Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 497190 |
| ensemblid | ENSG00000140839.13 |
| hgncid | 33849 |
| symbol | CLEC18B |
| name | C-type lectin domain family 18 member B |
| refseq_nuc | NM_001385193.1 |
| refseq_prot | NP_001372122.1 |
| ensembl_nuc | ENST00000682950.1 |
| ensembl_prot | ENSP00000507367.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 74408631 |
| end | 74421478 |
| strand | - |
| ver | v1.2 |
| region | chr16:74408631-74421478 |
| region5000 | chr16:74403631-74426478 |
| regionname0 | CLEC18B_chr16_74408631_74421478 |
| regionname5000 | CLEC18B_chr16_74403631_74426478 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 446 | 217 | 45 | 46 | 97 | 4 | 25 | 81 | CLEC18B_chr16_74403631_74426478 | CLEC18B | MLHPE others(441): Show |
chr16 | 74403631 | 74426478 |
| a0002 | 1/0 | 446 | 41 | 9 | 3 | 26 | 0 | 2 | 20 | CLEC18B_chr16_74403631_74426478 | CLEC18B | MLHPE others(441): Show |
chr16 | 74403631 | 74426478 |
| a0003 | 0/0 | 446 | 21 | 0 | 0 | 20 | 0 | 1 | 14 | CLEC18B_chr16_74403631_74426478 | CLEC18B | MLHPE others(441): Show |
chr16 | 74403631 | 74426478 |
| a0004 | 0/0 | 446 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | CLEC18B_chr16_74403631_74426478 | CLEC18B | MLHPE others(441): Show |
chr16 | 74403631 | 74426478 |
| a0005 | 0/0 | 14 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | MQGGS others(9): Show |
chr16 | 74403631 | 74426478 |
| a0006 | 0/0 | 446 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | MLHPE others(441): Show |
chr16 | 74403631 | 74426478 |
| a0007 | 0/0 | 446 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | MLHPE others(441): Show |
chr16 | 74403631 | 74426478 |
| a0008 | 0/0 | 181 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | MLHPE others(176): Show |
chr16 | 74403631 | 74426478 |
| a0009 | 0/0 | 446 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | MLHPE others(441): Show |
chr16 | 74403631 | 74426478 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1338 | 214 | 45 | 46 | 95 | 4 | 24 | CLEC18B_chr16_74403631_74426478 | CLEC18B | ATGCT others(1333): Show |
chr16 | 74403631 | 74426478 | ||
| a0001c0005 | 0/0 | 1338 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | ATGCT others(1333): Show |
chr16 | 74403631 | 74426478 | ||
| a0001c0008 | 0/0 | 1338 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | ATGCT others(1333): Show |
chr16 | 74403631 | 74426478 | ||
| a0002c0002 | 1/0 | 1338 | 40 | 8 | 3 | 26 | 0 | 2 | CLEC18B_chr16_74403631_74426478 | CLEC18B | ATGCT others(1333): Show |
chr16 | 74403631 | 74426478 | ||
| a0002c0009 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | ATGCT others(1333): Show |
chr16 | 74403631 | 74426478 | ||
| a0003c0003 | 0/0 | 1338 | 21 | 0 | 0 | 20 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | ATGCT others(1333): Show |
chr16 | 74403631 | 74426478 | ||
| a0004c0004 | 0/0 | 1338 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | ATGCT others(1333): Show |
chr16 | 74403631 | 74426478 | ||
| a0005c0012 | 0/0 | 882 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCGT others(877): Show |
chr16 | 74403631 | 74426478 | ||
| a0006c0011 | 0/0 | 1338 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | ATGCT others(1333): Show |
chr16 | 74403631 | 74426478 | ||
| a0007c0007 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | ATGCT others(1333): Show |
chr16 | 74403631 | 74426478 | ||
| a0008c0010 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | ATGCT others(1333): Show |
chr16 | 74403631 | 74426478 | ||
| a0009c0006 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | ATGCT others(1333): Show |
chr16 | 74403631 | 74426478 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1924 | 171 | 40 | 33 | 76 | 2 | 20 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0001c0001t0002 | 0/0 | 1924 | 41 | 5 | 12 | 19 | 2 | 3 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0001c0001t0004 | 0/0 | 1924 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0001c0001t0005 | 0/0 | 1924 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0001c0005t0001 | 0/0 | 1924 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0001c0008t0001 | 0/0 | 1924 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0002c0002t0001 | 1/0 | 1924 | 38 | 8 | 3 | 24 | 0 | 2 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0002c0002t0003 | 0/0 | 1924 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0002c0009t0001 | 0/0 | 1924 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0003c0003t0001 | 0/0 | 1924 | 21 | 0 | 0 | 20 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0004c0004t0001 | 0/0 | 1924 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0005c0012t0006 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCGT others(1255): Show |
chr16 | 74403631 | 74426478 |
| a0006c0011t0001 | 0/0 | 1924 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0007c0007t0001 | 0/0 | 1924 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0008c0010t0001 | 0/0 | 1924 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| a0009c0006t0002 | 0/0 | 1924 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | CTCTT others(1919): Show |
chr16 | 74403631 | 74426478 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 35 | 1 | 3 | 25 | 0 | 6 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0005 | 0/0 | 12 | 4 | 0 | 7 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0006 | 0/0 | 9 | 2 | 3 | 3 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0008 | 0/0 | 7 | 2 | 3 | 0 | 1 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 4 | 1 | 1 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0002g0002 | 0/0 | 34 | 4 | 11 | 16 | 1 | 2 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0005t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0001c0008t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0003 | 1/0 | 14 | 1 | 0 | 12 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0002t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0002c0009t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0003c0003t0001g0004 | 0/0 | 13 | 0 | 0 | 12 | 0 | 1 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0003c0003t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0004c0004t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0005c0012t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0006c0011t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0007c0007t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0008c0010t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| a0009c0006t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG00597 | hp1 | a0005 | c0012 | t0006 | g0036 | EAS | CHS | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG00738 | hp1 | a0006 | c0011 | t0001 | g0066 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0074 | EUR | IBS | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0099 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02027 | hp1 | a0004 | c0004 | t0001 | g0022 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0015 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02155 | hp1 | a0002 | c0002 | t0003 | g0026 | EAS | CDX | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | CDX | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02165 | hp2 | a0003 | c0003 | t0001 | g0107 | EAS | CDX | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | KHV | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03130 | hp2 | a0007 | c0007 | t0001 | g0103 | AFR | ESN | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03486 | hp2 | a0008 | c0010 | t0001 | g0062 | AFR | MSL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0101 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | BEB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG04199 | hp2 | a0001 | c0008 | t0001 | g0061 | SAS | STU | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | YRI | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | YRI | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | CHB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | CHB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18940 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18941 | hp1 | a0004 | c0004 | t0001 | g0022 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18951 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18953 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18954 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18965 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18977 | hp2 | a0001 | c0005 | t0001 | g0034 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18986 | hp2 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18990 | hp1 | a0003 | c0003 | t0001 | g0094 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18995 | hp2 | a0004 | c0004 | t0001 | g0022 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19059 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19065 | hp1 | a0001 | c0005 | t0001 | g0034 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19067 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19074 | hp1 | a0003 | c0003 | t0001 | g0100 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19075 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19089 | hp1 | a0009 | c0006 | t0002 | g0086 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19089 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ASW | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA20129 | hp2 | a0002 | c0009 | t0001 | g0057 | AFR | ASW | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | GIH | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0004 | SAS | GIH | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | USA | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | USA | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | USA | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0003 | REF | REF | CLEC18B_chr16_74403631_74426478 | CLEC18B | chr16 | 74403631 | 74426478 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74409026 | G | A | 1 | a0007 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1321C>T | p.Arg441Trp | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 12/12 | 1529/1924 | 1321/1341 | 441/446 | chr16 | 74409026 | |||
| chr16:74410926 | C | T | 1 | a0009 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.1093G>A | p.Glu365Lys | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 9/12 | 1301/1924 | 1093/1341 | 365/446 | chr16 | 74410926 | |||
| chr16:74410940 | A | G | 8 | a0001 a0003 a0004 others(5): Show |
246 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(243): Show |
missense_variant | MODERATE | c.1079T>C | p.Ile360Thr | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 9/12 | 1287/1924 | 1079/1341 | 360/446 | chr16 | 74410940 | |||
| chr16:74411718 | A | G | 2 | a0003 a0004 |
24 | HG02015.hp2 HG02027.hp1 HG02056.hp1 others(21): Show |
missense_variant | MODERATE | c.935T>C | p.Met312Thr | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 8/12 | 1143/1924 | 935/1341 | 312/446 | chr16 | 74411718 | |||
| chr16:74413587 | G | C | 1 | a0008 | 1 | HG03486.hp2 | stop_gained | HIGH | c.546C>G | p.Tyr182* | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 4/12 | 754/1924 | 546/1341 | 182/446 | chr16 | 74413587 | |||
| chr16:74413616 | T | C | 1 | a0006 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.517A>G | p.Thr173Ala | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 4/12 | 725/1924 | 517/1341 | 173/446 | chr16 | 74413616 | |||
| chr16:74413640 | G | A | 1 | a0004 | 3 | HG02027.hp1 NA18941.hp1 NA18995.hp2 |
missense_variant | MODERATE | c.493C>T | p.Arg165Trp | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 4/12 | 701/1924 | 493/1341 | 165/446 | chr16 | 74413640 | |||
| chr16:74416618 | GCCACCTT others(6286): Show |
G | 1 | a0005 | 1 | HG00597.hp1 | exon_loss_variant | HIGH | c.-1641_456+1440del | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/12 | chr16 | 74416618 | |||||||
| chr16:74421155 | A | T | 2 | a0002 a0003 |
3 | NA18997.hp1 NA19000.hp1 NA19067.hp2 |
missense_variant | MODERATE | c.116T>A | p.Met39Lys | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/12 | 324/1924 | 116/1341 | 39/446 | chr16 | 74421155 | |||
| chr16:74421201 | T | C | 2 | a0001 a0003 |
2 | NA20300.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.70A>G | p.Thr24Ala | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/12 | 278/1924 | 70/1341 | 24/446 | chr16 | 74421201 | |||
| chr16:74421239 | C | A | 1 | a0001 | 2 | HG02818.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.32G>T | p.Gly11Val | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/12 | 240/1924 | 32/1341 | 11/446 | chr16 | 74421239 | |||
| chr16:74421242 | C | T | 1 | a0001 | 2 | HG03139.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.29G>A | p.Arg10Gln | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/12 | 237/1924 | 29/1341 | 10/446 | chr16 | 74421242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74410927 | G | A | 1 | a0001c0008 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1092C>T | p.Phe364Phe | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 9/12 | 1300/1924 | 1092/1341 | 364/446 | chr16 | 74410927 | |||
| chr16:74410948 | G | A | 1 | a0001c0005 | 2 | NA18977.hp2 NA19065.hp1 |
synonymous_variant | LOW | c.1071C>T | p.Asn357Asn | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 9/12 | 1279/1924 | 1071/1341 | 357/446 | chr16 | 74410948 | |||
| chr16:74412837 | T | C | 1 | a0002c0009 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.720A>G | p.Gly240Gly | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 6/12 | 928/1924 | 720/1341 | 240/446 | chr16 | 74412837 | |||
| chr16:74418137 | C | T | 3 | a0001c0001 a0007c0007 a0009c0006 |
87 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(84): Show |
synonymous_variant | LOW | c.378G>A | p.Leu126Leu | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/12 | 586/1924 | 378/1341 | 126/446 | chr16 | 74418137 | |||
| chr16:74418149 | T | C | 1 | a0002c0002 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.366A>G | p.Glu122Glu | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/12 | 574/1924 | 366/1341 | 122/446 | chr16 | 74418149 | |||
| chr16:74418173 | G | A | 2 | a0001c0001 a0006c0011 |
11 | HG00738.hp1 HG01074.hp1 HG01099.hp2 others(8): Show |
synonymous_variant | LOW | c.342C>T | p.Pro114Pro | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/12 | 550/1924 | 342/1341 | 114/446 | chr16 | 74418173 | |||
| chr16:74418224 | C | T | 1 | a0001c0001 | 11 | HG00733.hp2 HG01255.hp2 HG01346.hp1 others(8): Show |
synonymous_variant | LOW | c.291G>A | p.Ala97Ala | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/12 | 499/1924 | 291/1341 | 97/446 | chr16 | 74418224 | |||
| chr16:74421193 | T | C | 1 | a0002c0002 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.78A>G | p.Ala26Ala | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/12 | 286/1924 | 78/1341 | 26/446 | chr16 | 74421193 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74408714 | A | G | 1 | a0001c0001t0005 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*292T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 12/12 | 292 | chr16 | 74408714 | ||||||
| chr16:74408814 | C | T | 1 | a0001c0001t0004 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*192G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 12/12 | 192 | chr16 | 74408814 | ||||||
| chr16:74408948 | A | G | 1 | a0002c0002t0003 | 2 | HG02155.hp1 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*58T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 12/12 | 58 | chr16 | 74408948 | ||||||
| chr16:74408983 | C | G | 2 | a0001c0001t0002 a0009c0006t0002 |
42 | HG00408.hp1 HG01255.hp1 HG01256.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 12/12 | 23 | chr16 | 74408983 | ||||||
| chr16:74421292 | C | T | 2 | a0001c0001t0001 a0002c0002t0001 |
3 | NA18522.hp2 NA18959.hp1 NA18982.hp2 |
5_prime_UTR_variant | MODIFIER | c.-22G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/12 | 22 | chr16 | 74421292 | ||||||
| chr16:74421293 | G | A | 1 | a0003c0003t0001 | 1 | NA20905.hp2 | 5_prime_UTR_variant | MODIFIER | c.-23C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/12 | 23 | chr16 | 74421293 | ||||||
| chr16:74421392 | GGGGGGCT others(14): Show |
G | 1 | a0003c0003t0001 | 1 | NA20905.hp2 | 5_prime_UTR_variant | MODIFIER | c.-143_-123delTTCTTT others(15): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/12 | 123 | chr16 | 74421392 | ||||||
| chr16:74421393 | G | C | 3 | a0001c0001t0001 a0001c0001t0002 a0009c0006t0002 |
40 | HG00408.hp1 HG01255.hp1 HG01256.hp1 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-123C>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/12 | 123 | chr16 | 74421393 | ||||||
| chr16:74421404 | A | G | 13 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(10): Show |
218 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(215): Show |
5_prime_UTR_variant | MODIFIER | c.-134T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/12 | 134 | chr16 | 74421404 | ||||||
| chr16:74421446 | G | A | 1 | a0001c0008t0001 | 1 | HG04199.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-176C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/12 | chr16 | 74421446 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:74409062 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1304-19C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 11/11 | chr16 | 74409062 | |||||||
| chr16:74409270 | A | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
240 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(237): Show |
intron_variant | MODIFIER | c.1304-227T>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 11/11 | chr16 | 74409270 | |||||||
| chr16:74409367 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1303+183G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 11/11 | chr16 | 74409367 | |||||||
| chr16:74409368 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1303+182C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 11/11 | chr16 | 74409368 | |||||||
| chr16:74409371 | A | G | 6 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0105 others(3): Show |
6 | HG00738.hp2 HG02818.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303+179T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 11/11 | chr16 | 74409371 | |||||||
| chr16:74409502 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1303+48G>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 11/11 | chr16 | 74409502 | |||||||
| chr16:74409503 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
248 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(245): Show |
intron_variant | MODIFIER | c.1303+47A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 11/11 | chr16 | 74409503 | |||||||
| chr16:74409511 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1303+39A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 11/11 | chr16 | 74409511 | |||||||
| chr16:74409644 | G | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0077 others(4): Show |
13 | HG00408.hp2 HG00733.hp2 HG01255.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1212-3C>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 10/11 | chr16 | 74409644 | |||||||
| chr16:74409753 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0044 |
10 | NA18951.hp1 NA18952.hp1 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.1212-112G>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 10/11 | chr16 | 74409753 | |||||||
| chr16:74409835 | T | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
239 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(236): Show |
intron_variant | MODIFIER | c.1212-194A>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 10/11 | chr16 | 74409835 | |||||||
| chr16:74409891 | T | TG | 46 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(43): Show |
120 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(117): Show |
intron_variant | MODIFIER | c.1212-251dupC | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 10/11 | chr16 | 74409891 | |||||||
| chr16:74409908 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0023 |
5 | HG00673.hp2 HG01109.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1212-267T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 10/11 | chr16 | 74409908 | |||||||
| chr16:74410119 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1211+417A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 10/11 | chr16 | 74410119 | |||||||
| chr16:74410185 | T | A | 46 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(43): Show |
120 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(117): Show |
intron_variant | MODIFIER | c.1211+351A>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 10/11 | chr16 | 74410185 | |||||||
| chr16:74410210 | T | G | 1 | a0003c0003t0001g0100 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1211+326A>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 10/11 | chr16 | 74410210 | |||||||
| chr16:74410321 | C | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0079 |
2 | HG00738.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1211+215G>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 10/11 | chr16 | 74410321 | |||||||
| chr16:74410340 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0077 others(5): Show |
14 | HG00408.hp2 HG00733.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.1211+196G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 10/11 | chr16 | 74410340 | |||||||
| chr16:74410639 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0045 a0001c0001t0001g0047 others(4): Show |
8 | HG01167.hp1 HG01167.hp2 HG01257.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1115-7G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 9/11 | chr16 | 74410639 | |||||||
| chr16:74410640 | G | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
106 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(103): Show |
splice_region_variant&intron_variant | LOW | c.1115-8C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 9/11 | chr16 | 74410640 | |||||||
| chr16:74410778 | C | T | 1 | a0007c0007t0001g0103 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1114+127G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 9/11 | chr16 | 74410778 | |||||||
| chr16:74410824 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1114+81G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 9/11 | chr16 | 74410824 | |||||||
| chr16:74411066 | T | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(57): Show |
136 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(133): Show |
intron_variant | MODIFIER | c.985-32A>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 8/11 | chr16 | 74411066 | |||||||
| chr16:74411284 | G | C | 23 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0028 others(20): Show |
32 | HG00408.hp2 HG00733.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.985-250C>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 8/11 | chr16 | 74411284 | |||||||
| chr16:74411294 | C | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(31): Show |
106 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(103): Show |
intron_variant | MODIFIER | c.985-260G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 8/11 | chr16 | 74411294 | |||||||
| chr16:74411399 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.984+270G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 8/11 | chr16 | 74411399 | |||||||
| chr16:74411470 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.984+199C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 8/11 | chr16 | 74411470 | |||||||
| chr16:74411476 | G | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.984+193C>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 8/11 | chr16 | 74411476 | |||||||
| chr16:74411576 | G | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0032 a0001c0001t0002g0074 others(4): Show |
41 | HG00408.hp1 HG01255.hp1 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.984+93C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 8/11 | chr16 | 74411576 | |||||||
| chr16:74411910 | T | C | 1 | a0005c0012t0006g0036 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.878-135A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 7/11 | chr16 | 74411910 | |||||||
| chr16:74411919 | C | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(74): Show |
212 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(209): Show |
intron_variant | MODIFIER | c.878-144G>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 7/11 | chr16 | 74411919 | |||||||
| chr16:74412050 | G | T | 1 | a0001c0001t0001g0029 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.877+104C>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 7/11 | chr16 | 74412050 | |||||||
| chr16:74412146 | G | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(30): Show |
104 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(101): Show |
splice_region_variant&intron_variant | LOW | c.877+8C>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 7/11 | chr16 | 74412146 | |||||||
| chr16:74412146 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG01975.hp2 | splice_region_variant&intron_variant | LOW | c.877+8C>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 7/11 | chr16 | 74412146 | |||||||
| chr16:74412373 | C | T | 1 | a0007c0007t0001g0103 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.785-127G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 6/11 | chr16 | 74412373 | |||||||
| chr16:74412400 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.785-154C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 6/11 | chr16 | 74412400 | |||||||
| chr16:74412443 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.785-197A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 6/11 | chr16 | 74412443 | |||||||
| chr16:74412531 | T | C | 1 | a0002c0002t0001g0059 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.784+242A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 6/11 | chr16 | 74412531 | |||||||
| chr16:74412564 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.784+209G>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 6/11 | chr16 | 74412564 | |||||||
| chr16:74412891 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.677-11C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 5/11 | chr16 | 74412891 | |||||||
| chr16:74412932 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.677-52C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 5/11 | chr16 | 74412932 | |||||||
| chr16:74413226 | C | CT | 18 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0069 others(15): Show |
54 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(51): Show |
intron_variant | MODIFIER | c.555-69dupA | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 4/11 | chr16 | 74413226 | |||||||
| chr16:74413226 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0023 others(1): Show |
18 | HG00597.hp2 HG00673.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.555-68G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 4/11 | chr16 | 74413226 | |||||||
| chr16:74413404 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0093 a0001c0001t0001g0096 others(3): Show |
6 | HG00408.hp2 HG02818.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.554+175G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 4/11 | chr16 | 74413404 | |||||||
| chr16:74413441 | C | A | 1 | a0001c0001t0001g0021 | 3 | NA18957.hp2 NA18981.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.554+138G>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 4/11 | chr16 | 74413441 | |||||||
| chr16:74413810 | G | A | 1 | a0001c0008t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.457-134C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74413810 | |||||||
| chr16:74413849 | C | CTTAT | 6 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0049 others(3): Show |
25 | HG00597.hp2 HG01891.hp2 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.457-177_457-174dup others(4): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74413849 | |||||||
| chr16:74413849 | C | CTTATTTA others(1): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0037 |
3 | HG00673.hp2 HG01109.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.457-181_457-174dup others(8): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74413849 | |||||||
| chr16:74413849 | C | CTTTT | 3 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0092 |
6 | HG02896.hp1 HG02897.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-174_457-173ins others(4): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74413849 | |||||||
| chr16:74413849 | C | CTTTTTTA others(1): Show |
12 | a0001c0001t0001g0064 a0001c0001t0001g0077 a0001c0001t0001g0079 others(9): Show |
13 | HG00408.hp1 HG00408.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.457-174_457-173ins others(8): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74413849 | |||||||
| chr16:74413849 | C | CTTTTTTA others(5): Show |
33 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(30): Show |
129 | HG00642.hp2 HG00673.hp1 HG00738.hp1 others(126): Show |
intron_variant | MODIFIER | c.457-174_457-173ins others(12): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74413849 | |||||||
| chr16:74413849 | C | CTTTTTTA others(9): Show |
17 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0028 others(14): Show |
34 | HG00597.hp1 HG00738.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.457-174_457-173ins others(16): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74413849 | |||||||
| chr16:74413849 | C | CTTTTTTA others(13): Show |
4 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0084 others(1): Show |
4 | HG01069.hp2 NA18989.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.457-174_457-173ins others(20): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74413849 | |||||||
| chr16:74413849 | C | CTTTTTTA others(17): Show |
1 | a0001c0001t0001g0102 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.457-174_457-173ins others(24): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74413849 | |||||||
| chr16:74413849 | CTTAT | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(14): Show |
38 | HG00642.hp1 HG00733.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.457-177_457-174del others(4): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74413849 | |||||||
| chr16:74413881 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0007c0007t0001g0103 |
4 | HG02896.hp1 HG02897.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.457-205A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74413881 | |||||||
| chr16:74414127 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0023 others(16): Show |
69 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.457-451C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74414127 | |||||||
| chr16:74414200 | G | T | 2 | a0001c0001t0001g0063 a0008c0010t0001g0062 |
2 | HG00738.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.457-524C>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74414200 | |||||||
| chr16:74414278 | G | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0019 others(22): Show |
41 | HG00597.hp1 HG00738.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.457-602C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74414278 | |||||||
| chr16:74414327 | G | C | 1 | a0005c0012t0006g0036 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.457-651C>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74414327 | |||||||
| chr16:74414328 | T | C | 1 | a0005c0012t0006g0036 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.457-652A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74414328 | |||||||
| chr16:74414419 | T | A | 16 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0073 others(13): Show |
52 | HG00408.hp1 HG01167.hp1 HG01169.hp1 others(49): Show |
intron_variant | MODIFIER | c.457-743A>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74414419 | |||||||
| chr16:74414528 | A | G | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(30): Show |
65 | HG00597.hp2 HG00673.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.457-852T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74414528 | |||||||
| chr16:74414578 | G | A | 1 | a0005c0012t0006g0036 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.457-902C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74414578 | |||||||
| chr16:74414954 | A | G | 2 | a0001c0008t0001g0061 a0005c0012t0006g0036 |
2 | HG00597.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.457-1278T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74414954 | |||||||
| chr16:74415003 | A | G | 1 | a0002c0002t0001g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.457-1327T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415003 | |||||||
| chr16:74415120 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | HG01167.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.457-1444C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415120 | |||||||
| chr16:74415149 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0023 others(7): Show |
26 | HG00597.hp2 HG00673.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.457-1473T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415149 | |||||||
| chr16:74415273 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.457-1597A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415273 | |||||||
| chr16:74415325 | C | A | 7 | a0001c0001t0002g0002 a0001c0001t0002g0032 a0001c0001t0002g0074 others(4): Show |
41 | HG00408.hp1 HG01255.hp1 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.457-1649G>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415325 | |||||||
| chr16:74415496 | A | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
105 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.457-1820T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415496 | |||||||
| chr16:74415526 | C | T | 1 | a0001c0008t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.457-1850G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415526 | |||||||
| chr16:74415527 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.457-1851C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415527 | |||||||
| chr16:74415576 | A | T | 1 | a0005c0012t0006g0036 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.457-1900T>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415576 | |||||||
| chr16:74415587 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.457-1911A>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415587 | |||||||
| chr16:74415601 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.457-1925A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415601 | |||||||
| chr16:74415705 | C | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
198 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(195): Show |
intron_variant | MODIFIER | c.457-2029G>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415705 | |||||||
| chr16:74415824 | T | C | 1 | a0002c0002t0001g0075 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.457-2148A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415824 | |||||||
| chr16:74415853 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.457-2177C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415853 | |||||||
| chr16:74415920 | A | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
106 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.456+2139T>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74415920 | |||||||
| chr16:74416117 | G | A | 1 | a0005c0012t0006g0036 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.456+1942C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416117 | |||||||
| chr16:74416120 | G | A | 1 | a0003c0003t0001g0107 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.456+1939C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416120 | |||||||
| chr16:74416220 | A | G | 2 | a0001c0001t0001g0089 a0005c0012t0006g0036 |
2 | HG00597.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.456+1839T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416220 | |||||||
| chr16:74416232 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(34): Show |
107 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.456+1827G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416232 | |||||||
| chr16:74416234 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.456+1825C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416234 | |||||||
| chr16:74416249 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.456+1810G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416249 | |||||||
| chr16:74416250 | G | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
106 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.456+1809C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416250 | |||||||
| chr16:74416262 | C | CA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(45): Show |
160 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.456+1796dupT | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416262 | |||||||
| chr16:74416262 | C | CAA | 3 | a0001c0001t0001g0035 a0001c0001t0002g0108 a0003c0003t0001g0015 |
7 | HG02056.hp1 HG02135.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.456+1795_456+1796d others(4): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416262 | |||||||
| chr16:74416262 | CA | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
6 | HG01069.hp2 HG01433.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.456+1796delT | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416262 | |||||||
| chr16:74416345 | C | G | 1 | a0001c0001t0001g0038 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.456+1714G>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416345 | |||||||
| chr16:74416375 | GTTC | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0023 others(1): Show |
18 | HG00597.hp2 HG00673.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.456+1681_456+1683d others(5): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416375 | |||||||
| chr16:74416390 | G | A | 1 | a0005c0012t0006g0036 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.456+1669C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416390 | |||||||
| chr16:74416434 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.456+1625C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416434 | |||||||
| chr16:74416672 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.456+1387G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416672 | |||||||
| chr16:74416949 | G | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0077 others(3): Show |
13 | HG00733.hp2 HG01255.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.456+1110C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74416949 | |||||||
| chr16:74417002 | A | G | 1 | a0001c0008t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.456+1057T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417002 | |||||||
| chr16:74417103 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.456+956T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417103 | |||||||
| chr16:74417149 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(34): Show |
117 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(114): Show |
intron_variant | MODIFIER | c.456+910G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417149 | |||||||
| chr16:74417170 | C | G | 1 | a0001c0001t0005g0043 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.456+889G>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417170 | |||||||
| chr16:74417359 | C | T | 36 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(33): Show |
82 | HG00408.hp1 HG00738.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.456+700G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417359 | |||||||
| chr16:74417467 | G | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(21): Show |
88 | HG00642.hp2 HG00673.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.456+592C>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417467 | |||||||
| chr16:74417483 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0077 others(3): Show |
12 | HG00733.hp2 HG01255.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.456+576G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417483 | |||||||
| chr16:74417849 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.456+210G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417849 | |||||||
| chr16:74417878 | A | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0019 others(19): Show |
33 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.456+181T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417878 | |||||||
| chr16:74417883 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0058 |
2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.456+176T>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417883 | |||||||
| chr16:74417917 | CA | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(52): Show |
131 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(128): Show |
intron_variant | MODIFIER | c.456+141delT | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417917 | |||||||
| chr16:74417929 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0096 |
2 | HG00408.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.456+130T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417929 | |||||||
| chr16:74417986 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(34): Show |
107 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.456+73G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74417986 | |||||||
| chr16:74418033 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0077 others(2): Show |
11 | HG00733.hp2 HG01255.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.456+26C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74418033 | |||||||
| chr16:74418036 | G | GGCCTCAC others(13): Show |
1 | a0003c0003t0001g0004 | 2 | NA18942.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.456+3_456+22dupGAG others(17): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 3/11 | chr16 | 74418036 | |||||||
| chr16:74418370 | C | T | 1 | a0001c0008t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.217-72G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74418370 | |||||||
| chr16:74418392 | C | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0093 a0001c0001t0001g0096 others(3): Show |
6 | HG00408.hp2 HG01069.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.217-94G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74418392 | |||||||
| chr16:74418572 | T | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0005t0001g0034 |
10 | HG02155.hp2 NA18939.hp2 NA18977.hp2 others(7): Show |
intron_variant | MODIFIER | c.217-274A>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74418572 | |||||||
| chr16:74418799 | CT | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(15): Show |
22 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.217-502delA | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74418799 | |||||||
| chr16:74418872 | C | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(30): Show |
98 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(95): Show |
intron_variant | MODIFIER | c.217-574G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74418872 | |||||||
| chr16:74418983 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.217-685C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74418983 | |||||||
| chr16:74419012 | G | C | 1 | a0001c0008t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.217-714C>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419012 | |||||||
| chr16:74419194 | G | A | 1 | a0001c0001t0001g0005 | 3 | HG02132.hp2 NA19057.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.217-896C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419194 | |||||||
| chr16:74419208 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0077 others(3): Show |
12 | HG00733.hp2 HG01255.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-910G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419208 | |||||||
| chr16:74419430 | T | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0041 others(14): Show |
24 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.216+1071A>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419430 | |||||||
| chr16:74419496 | C | T | 1 | a0001c0008t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.216+1005G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419496 | |||||||
| chr16:74419501 | T | C | 11 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(8): Show |
45 | HG00408.hp1 HG01255.hp1 HG01256.hp1 others(42): Show |
intron_variant | MODIFIER | c.216+1000A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419501 | |||||||
| chr16:74419555 | T | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0096 |
2 | HG00408.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.216+946A>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419555 | |||||||
| chr16:74419644 | C | G | 1 | a0003c0003t0001g0015 | 2 | NA18983.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.216+857G>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419644 | |||||||
| chr16:74419710 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0077 others(4): Show |
13 | HG00733.hp2 HG01255.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+791C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419710 | |||||||
| chr16:74419913 | G | A | 1 | a0002c0002t0001g0007 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.216+588C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419913 | |||||||
| chr16:74419915 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.216+586G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419915 | |||||||
| chr16:74419922 | T | C | 9 | a0001c0001t0001g0020 a0001c0001t0002g0002 a0001c0001t0002g0032 others(6): Show |
43 | HG00408.hp1 HG01255.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.216+579A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419922 | |||||||
| chr16:74419961 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0058 |
2 | HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.216+540C>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419961 | |||||||
| chr16:74419972 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.216+529G>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74419972 | |||||||
| chr16:74420051 | A | C | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0002c0002t0001g0017 |
3 | HG00733.hp1 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.216+450T>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74420051 | |||||||
| chr16:74420093 | G | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(25): Show |
95 | HG00642.hp2 HG00673.hp1 HG01099.hp1 others(92): Show |
intron_variant | MODIFIER | c.216+408C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74420093 | |||||||
| chr16:74420142 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0005t0001g0034 |
10 | HG02155.hp2 NA18939.hp2 NA18977.hp2 others(7): Show |
intron_variant | MODIFIER | c.216+359C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74420142 | |||||||
| chr16:74420159 | G | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0033 a0001c0001t0001g0077 others(4): Show |
12 | HG00408.hp2 HG00733.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.216+342C>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74420159 | |||||||
| chr16:74420187 | A | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0016 others(25): Show |
84 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.216+314T>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74420187 | |||||||
| chr16:74420290 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.216+211G>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74420290 | |||||||
| chr16:74420365 | G | A | 3 | a0002c0002t0001g0027 a0003c0003t0001g0094 a0004c0004t0001g0022 |
3 | HG02723.hp1 NA18941.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.216+136C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74420365 | |||||||
| chr16:74420454 | G | A | 1 | a0001c0001t0005g0043 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.216+47C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 2/11 | chr16 | 74420454 | |||||||
| chr16:74420602 | G | T | 1 | a0002c0002t0001g0007 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.125-10C>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74420602 | |||||||
| chr16:74420623 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0033 others(4): Show |
14 | HG00408.hp2 HG00733.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.125-31C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74420623 | |||||||
| chr16:74420652 | G | A | 2 | a0002c0002t0001g0017 a0002c0009t0001g0057 |
3 | HG01109.hp1 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.125-60C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74420652 | |||||||
| chr16:74420659 | T | C | 1 | a0001c0001t0001g0014 | 3 | NA18951.hp1 NA18983.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.125-67A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74420659 | |||||||
| chr16:74420848 | C | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0090 |
2 | NA18959.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.125-256G>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74420848 | |||||||
| chr16:74420940 | GTCCTCCT others(3): Show |
G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(79): Show |
217 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(214): Show |
intron_variant | MODIFIER | c.124+197_124+206del others(10): Show |
CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74420940 | |||||||
| chr16:74421005 | G | A | 1 | a0001c0001t0001g0010 | 5 | HG02083.hp2 NA18939.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+142C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74421005 | |||||||
| chr16:74421009 | G | A | 1 | a0002c0002t0001g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.124+138C>T | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74421009 | |||||||
| chr16:74421035 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.124+112G>A | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74421035 | |||||||
| chr16:74421036 | C | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(19): Show |
39 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.124+111G>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74421036 | |||||||
| chr16:74421105 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(62): Show |
184 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(181): Show |
intron_variant | MODIFIER | c.124+42T>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74421105 | |||||||
| chr16:74421125 | C | G | 1 | a0001c0008t0001g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.124+22G>C | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74421125 | |||||||
| chr16:74421126 | T | C | 1 | a0002c0002t0001g0017 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.124+21A>G | CLEC18B | ENSG00000140839.13 | transcript | ENST00000682950.1 | protein_coding | 1/11 | chr16 | 74421126 |