Item | Value |
---|---|
geneid | 283971 |
ensemblid | ENSG00000157335.21 |
hgncid | 28538 |
symbol | CLEC18C |
name | C-type lectin domain family 18 member C |
refseq_nuc | NM_173619.4 |
refseq_prot | NP_775890.2 |
ensembl_nuc | ENST00000541793.7 |
ensembl_prot | ENSP00000444875.2 |
mane_status | MANE Select |
chr | chr16 |
start | 70173787 |
end | 70186895 |
strand | + |
ver | v1.2 |
region | chr16:70173787-70186895 |
region5000 | chr16:70168787-70191895 |
regionname0 | CLEC18C_chr16_70173787_70186895 |
regionname5000 | CLEC18C_chr16_70168787_70191895 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 446 | 157 | 40 | 34 | 66 | 1 | 16 | 51 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0002 | 0/0 | 446 | 63 | 2 | 19 | 34 | 3 | 5 | 19 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0003 | 1/0 | 446 | 47 | 1 | 16 | 10 | 4 | 15 | 8 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0004 | 0/0 | 446 | 27 | 27 | 0 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0005 | 0/0 | 446 | 17 | 1 | 3 | 5 | 3 | 5 | 3 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0006 | 0/0 | 446 | 10 | 0 | 0 | 10 | 0 | 0 | 7 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0007 | 0/0 | 446 | 9 | 0 | 0 | 9 | 0 | 0 | 3 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0008 | 0/0 | 446 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0009 | 0/0 | 445 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(440): Show |
chr16 | 70168787 | 70191895 |
a0010 | 0/0 | 446 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0011 | 0/0 | 446 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0012 | 0/0 | 446 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0013 | 0/0 | 446 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0014 | 0/0 | 446 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0015 | 0/0 | 446 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0016 | 0/0 | 171 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(166): Show |
chr16 | 70168787 | 70191895 |
a0017 | 0/0 | 446 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0018 | 0/0 | 446 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0019 | 0/0 | 446 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0020 | 0/0 | 446 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0021 | 0/0 | 446 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0022 | 0/0 | 446 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0023 | 0/0 | 446 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0024 | 0/0 | 446 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0025 | 0/0 | 446 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
a0026 | 0/0 | 446 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | MLHPE others(441): Show |
chr16 | 70168787 | 70191895 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1338 | 157 | 40 | 34 | 66 | 1 | 16 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0002c0002 | 0/0 | 1338 | 61 | 2 | 18 | 34 | 2 | 5 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0002c0011 | 0/0 | 1338 | 2 | 0 | 1 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0003c0003 | 1/0 | 1338 | 47 | 1 | 16 | 10 | 4 | 15 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0004c0004 | 0/0 | 1338 | 21 | 21 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0004c0008 | 0/0 | 1338 | 5 | 5 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0004c0029 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0005c0005 | 0/0 | 1338 | 17 | 1 | 3 | 5 | 3 | 5 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0006c0006 | 0/0 | 1338 | 10 | 0 | 0 | 10 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0007c0007 | 0/0 | 1338 | 9 | 0 | 0 | 9 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0008c0009 | 0/0 | 1338 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0009c0010 | 0/0 | 1335 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1330): Show |
chr16 | 70168787 | 70191895 | ||
a0010c0012 | 0/0 | 1338 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0011c0026 | 0/0 | 1338 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0012c0020 | 0/0 | 1338 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0013c0027 | 0/0 | 1338 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0014c0016 | 0/0 | 1338 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0015c0023 | 0/0 | 1338 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0016c0018 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0017c0025 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0018c0021 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0019c0028 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0020c0024 | 0/0 | 1338 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0021c0022 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0022c0015 | 0/0 | 1338 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0023c0019 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0024c0013 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0025c0014 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 | ||
a0026c0017 | 0/0 | 1338 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | ATGCT others(1333): Show |
chr16 | 70168787 | 70191895 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1987 | 78 | 7 | 21 | 41 | 0 | 9 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0001c0001t0003 | 0/0 | 1987 | 49 | 29 | 8 | 8 | 1 | 3 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0001c0001t0004 | 0/0 | 1987 | 19 | 1 | 0 | 16 | 0 | 2 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0001c0001t0008 | 0/0 | 1987 | 4 | 0 | 4 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0001c0001t0009 | 0/0 | 1987 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0001c0001t0011 | 0/0 | 1987 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0001c0001t0013 | 0/0 | 1987 | 2 | 0 | 1 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0001c0001t0018 | 0/0 | 1987 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0001c0001t0020 | 0/0 | 1987 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0002c0002t0002 | 0/0 | 1987 | 55 | 2 | 15 | 31 | 2 | 5 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0002c0002t0010 | 0/0 | 1987 | 3 | 0 | 2 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0002c0002t0012 | 0/0 | 1987 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0002c0002t0019 | 0/0 | 1987 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0002c0011t0002 | 0/0 | 1987 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0002c0011t0017 | 0/0 | 1987 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0003c0003t0001 | 1/0 | 1987 | 45 | 1 | 16 | 9 | 3 | 15 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0003c0003t0009 | 0/0 | 1987 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0003c0003t0016 | 0/0 | 1987 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0004c0004t0005 | 0/0 | 1987 | 8 | 8 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0004c0004t0006 | 0/0 | 1987 | 13 | 13 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0004c0008t0005 | 0/0 | 1987 | 5 | 5 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0004c0029t0006 | 0/0 | 1987 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0005c0005t0001 | 0/0 | 1987 | 16 | 1 | 2 | 5 | 3 | 5 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0005c0005t0009 | 0/0 | 1987 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0006c0006t0001 | 0/0 | 1987 | 10 | 0 | 0 | 10 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0007c0007t0004 | 0/0 | 1987 | 9 | 0 | 0 | 9 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0008c0009t0007 | 0/0 | 1987 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0009c0010t0005 | 0/0 | 1984 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1979): Show |
chr16 | 70168787 | 70191895 |
a0010c0012t0001 | 0/0 | 1987 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0011c0026t0009 | 0/0 | 1987 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0012c0020t0022 | 0/0 | 1987 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0013c0027t0005 | 0/0 | 1987 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0014c0016t0010 | 0/0 | 1987 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0015c0023t0001 | 0/0 | 1987 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0016c0018t0007 | 0/0 | 1987 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0017c0025t0014 | 0/0 | 1987 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0018c0021t0003 | 0/0 | 1987 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0019c0028t0006 | 0/0 | 1987 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0020c0024t0004 | 0/0 | 1987 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0021c0022t0003 | 0/0 | 1987 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0022c0015t0021 | 0/0 | 1987 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0023c0019t0001 | 0/0 | 1987 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0024c0013t0015 | 0/0 | 1987 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0025c0014t0002 | 0/0 | 1987 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
a0026c0017t0002 | 0/0 | 1987 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | GCCCA others(1982): Show |
chr16 | 70168787 | 70191895 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0004 | 0/0 | 11 | 0 | 4 | 6 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0007 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0008 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0009 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0004g0005 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0004g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0008g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0009g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0011g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0013g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0013g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0018g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0001c0001t0020g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0002 | 0/0 | 21 | 0 | 1 | 17 | 1 | 2 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0010 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0010g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0012g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0002t0019g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0011t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0002c0011t0017g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0001 | 0/0 | 23 | 1 | 9 | 1 | 1 | 11 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0009g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0003c0003t0016g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0006g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0006g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0004t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0008t0005g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0008t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0008t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0004c0029t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0005c0005t0001g0003 | 0/0 | 8 | 0 | 1 | 2 | 1 | 4 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0005c0005t0001g0035 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0005c0005t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0005c0005t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0005c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0005c0005t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0005c0005t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0005c0005t0009g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0006c0006t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0006c0006t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0006c0006t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0006c0006t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0006c0006t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0007c0007t0004g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0007c0007t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0007c0007t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0007c0007t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0007c0007t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0008c0009t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0008c0009t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0008c0009t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0008c0009t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0009c0010t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0010c0012t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0010c0012t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0011c0026t0009g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0012c0020t0022g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0013c0027t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0014c0016t0010g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0015c0023t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0016c0018t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0017c0025t0014g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0018c0021t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0019c0028t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0020c0024t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0021c0022t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0022c0015t0021g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0023c0019t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0024c0013t0015g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0025c0014t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
a0026c0017t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0005 | c0005 | t0001 | g0003 | EUR | GBR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00140 | hp2 | a0011 | c0026 | t0009 | g0117 | EUR | GBR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00323 | hp1 | a0005 | c0005 | t0001 | g0138 | EUR | FIN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0095 | EUR | FIN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00423 | hp2 | a0007 | c0007 | t0004 | g0013 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00558 | hp1 | a0007 | c0007 | t0004 | g0013 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00558 | hp2 | a0002 | c0002 | t0010 | g0021 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00597 | hp1 | a0003 | c0003 | t0001 | g0175 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00621 | hp1 | a0006 | c0006 | t0001 | g0023 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00621 | hp2 | a0005 | c0005 | t0001 | g0003 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00639 | hp2 | a0012 | c0020 | t0022 | g0179 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00642 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00735 | hp2 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00738 | hp1 | a0002 | c0002 | t0010 | g0021 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0034 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01069 | hp1 | a0010 | c0012 | t0001 | g0188 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0100 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01071 | hp1 | a0010 | c0012 | t0001 | g0189 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0153 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01099 | hp1 | a0002 | c0002 | t0002 | g0076 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01099 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0132 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01167 | hp2 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01169 | hp1 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01169 | hp2 | a0002 | c0002 | t0019 | g0068 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01175 | hp1 | a0002 | c0002 | t0010 | g0021 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01192 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0012 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0142 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01255 | hp2 | a0002 | c0011 | t0017 | g0047 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01256 | hp1 | a0003 | c0003 | t0001 | g0140 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0083 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01346 | hp2 | a0005 | c0005 | t0001 | g0003 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01358 | hp2 | a0001 | c0001 | t0013 | g0178 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0149 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01433 | hp1 | a0013 | c0027 | t0005 | g0115 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01496 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01515 | hp1 | a0002 | c0011 | t0002 | g0062 | EUR | IBS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01515 | hp2 | a0003 | c0003 | t0016 | g0001 | EUR | IBS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0009 | EUR | IBS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0166 | EUR | IBS | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0028 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01891 | hp1 | a0004 | c0004 | t0006 | g0105 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01891 | hp2 | a0004 | c0004 | t0006 | g0097 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01928 | hp1 | a0003 | c0003 | t0001 | g0176 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01934 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01943 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01943 | hp2 | a0014 | c0016 | t0010 | g0145 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0058 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01975 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0060 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0067 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01993 | hp1 | a0003 | c0003 | t0001 | g0168 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02015 | hp1 | a0005 | c0005 | t0001 | g0003 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02040 | hp1 | a0001 | c0001 | t0020 | g0025 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02040 | hp2 | a0002 | c0002 | t0012 | g0002 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02055 | hp1 | a0004 | c0004 | t0005 | g0111 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02071 | hp1 | a0006 | c0006 | t0001 | g0163 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02080 | hp1 | a0007 | c0007 | t0004 | g0013 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02083 | hp2 | a0007 | c0007 | t0004 | g0192 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02132 | hp2 | a0007 | c0007 | t0004 | g0126 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02135 | hp2 | a0002 | c0002 | t0012 | g0002 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02148 | hp2 | a0015 | c0023 | t0001 | g0154 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02165 | hp2 | a0003 | c0003 | t0001 | g0170 | EAS | CDX | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02258 | hp1 | a0004 | c0008 | t0005 | g0016 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02258 | hp2 | a0005 | c0005 | t0001 | g0035 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02273 | hp1 | a0005 | c0005 | t0009 | g0090 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02273 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02280 | hp2 | a0004 | c0004 | t0006 | g0099 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02300 | hp1 | a0005 | c0005 | t0001 | g0185 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02451 | hp1 | a0008 | c0009 | t0007 | g0124 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02451 | hp2 | a0004 | c0004 | t0006 | g0015 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02523 | hp2 | a0006 | c0006 | t0001 | g0003 | EAS | KHV | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02572 | hp1 | a0017 | c0025 | t0014 | g0108 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02602 | hp1 | a0005 | c0005 | t0001 | g0003 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02602 | hp2 | a0005 | c0005 | t0001 | g0003 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02647 | hp1 | a0004 | c0004 | t0005 | g0113 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02647 | hp2 | a0001 | c0001 | t0018 | g0182 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02698 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02698 | hp2 | a0003 | c0003 | t0001 | g0034 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02717 | hp2 | a0008 | c0009 | t0007 | g0123 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02723 | hp1 | a0009 | c0010 | t0005 | g0020 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02723 | hp2 | a0004 | c0004 | t0006 | g0031 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0078 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0079 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02738 | hp2 | a0001 | c0001 | t0009 | g0131 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02809 | hp2 | a0004 | c0004 | t0006 | g0031 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02818 | hp1 | a0009 | c0010 | t0005 | g0020 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02886 | hp1 | a0004 | c0004 | t0006 | g0098 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02896 | hp1 | a0004 | c0008 | t0005 | g0101 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02922 | hp1 | a0004 | c0004 | t0005 | g0016 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02922 | hp2 | a0004 | c0004 | t0006 | g0015 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02965 | hp1 | a0004 | c0029 | t0006 | g0104 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02970 | hp1 | a0004 | c0008 | t0005 | g0016 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02970 | hp2 | a0018 | c0021 | t0003 | g0081 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03017 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03098 | hp2 | a0019 | c0028 | t0006 | g0103 | AFR | MSL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03130 | hp2 | a0004 | c0004 | t0006 | g0107 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03195 | hp1 | a0004 | c0004 | t0006 | g0015 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | MSL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03225 | hp2 | a0001 | c0001 | t0011 | g0028 | AFR | MSL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03239 | hp1 | a0020 | c0024 | t0004 | g0026 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03486 | hp1 | a0004 | c0004 | t0006 | g0116 | AFR | MSL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03486 | hp2 | a0009 | c0010 | t0005 | g0020 | AFR | MSL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03490 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03492 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03492 | hp2 | a0003 | c0003 | t0001 | g0190 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03516 | hp1 | a0004 | c0008 | t0005 | g0016 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03516 | hp2 | a0021 | c0022 | t0003 | g0089 | AFR | ESN | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03540 | hp2 | a0008 | c0009 | t0007 | g0121 | AFR | GWD | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | MSL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03579 | hp2 | a0004 | c0004 | t0005 | g0118 | AFR | MSL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0119 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03669 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | STU | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0072 | SAS | PJL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03831 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | BEB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03834 | hp1 | a0005 | c0005 | t0001 | g0003 | SAS | BEB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03834 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | BEB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03927 | hp1 | a0001 | c0001 | t0013 | g0012 | SAS | BEB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0005 | SAS | BEB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG04199 | hp1 | a0005 | c0005 | t0001 | g0003 | SAS | STU | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG04199 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | STU | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG04204 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | STU | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG04228 | hp1 | a0005 | c0005 | t0001 | g0151 | SAS | STU | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG04228 | hp2 | a0003 | c0003 | t0001 | g0194 | SAS | STU | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18612 | hp1 | a0007 | c0007 | t0004 | g0013 | EAS | CHB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18612 | hp2 | a0023 | c0019 | t0001 | g0157 | EAS | CHB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18906 | hp1 | a0004 | c0004 | t0006 | g0096 | AFR | YRI | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18906 | hp2 | a0004 | c0004 | t0005 | g0114 | AFR | YRI | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18939 | hp2 | a0005 | c0005 | t0001 | g0125 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18943 | hp1 | a0024 | c0013 | t0015 | g0046 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18943 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18946 | hp1 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18952 | hp2 | a0006 | c0006 | t0001 | g0003 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18960 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18962 | hp2 | a0007 | c0007 | t0004 | g0193 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18971 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18976 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18976 | hp2 | a0006 | c0006 | t0001 | g0161 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18981 | hp1 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18983 | hp2 | a0006 | c0006 | t0001 | g0023 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18985 | hp1 | a0006 | c0006 | t0001 | g0023 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18986 | hp2 | a0006 | c0006 | t0001 | g0003 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18987 | hp1 | a0005 | c0005 | t0001 | g0043 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA18997 | hp2 | a0025 | c0014 | t0002 | g0065 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19003 | hp1 | a0026 | c0017 | t0002 | g0052 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19007 | hp2 | a0005 | c0005 | t0001 | g0043 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19009 | hp2 | a0007 | c0007 | t0004 | g0191 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19012 | hp2 | a0007 | c0007 | t0004 | g0013 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | LWK | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | LWK | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19057 | hp2 | a0003 | c0003 | t0009 | g0174 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19065 | hp1 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19083 | hp2 | a0006 | c0006 | t0001 | g0041 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19089 | hp1 | a0006 | c0006 | t0001 | g0041 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA20129 | hp1 | a0004 | c0004 | t0005 | g0112 | AFR | ASW | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ASW | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | TSI | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA20752 | hp2 | a0003 | c0003 | t0001 | g0167 | EUR | TSI | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA20805 | hp1 | a0005 | c0005 | t0001 | g0035 | EUR | TSI | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA20805 | hp2 | a0003 | c0003 | t0001 | g0001 | EUR | TSI | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA20905 | hp1 | a0003 | c0003 | t0001 | g0144 | SAS | GIH | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | GIH | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0094 | AMR | CLM | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02109 | hp1 | a0008 | c0009 | t0007 | g0120 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02109 | hp2 | a0004 | c0004 | t0006 | g0015 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02486 | hp1 | a0016 | c0018 | t0007 | g0122 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02559 | hp1 | a0004 | c0008 | t0005 | g0110 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | ACB | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03471 | hp1 | a0004 | c0004 | t0005 | g0106 | AFR | MSL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | MSL | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG06807 | hp1 | a0022 | c0015 | t0021 | g0102 | AFR | USA | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | USA | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA20300 | hp1 | a0003 | c0003 | t0001 | g0001 | AFR | USA | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA20300 | hp2 | a0004 | c0004 | t0005 | g0109 | AFR | USA | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | LWK | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0136 | REF | REF | CLEC18C_chr16_70168787_70191895 | CLEC18C | chr16 | 70168787 | 70191895 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:70174348 | G | A | 2 | a0007 a0024 |
10 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(7): Show |
missense_variant | MODERATE | c.70G>A | p.Ala24Thr | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/13 | 341/1987 | 70/1341 | 24/446 | chr16 | 70174348 | |||
chr16:70177274 | G | A | 1 | a0022 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.250G>A | p.Ala84Thr | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 521/1987 | 250/1341 | 84/446 | chr16 | 70177274 | |||
chr16:70177281 | C | T | 1 | a0020 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.257C>T | p.Ala86Val | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 528/1987 | 257/1341 | 86/446 | chr16 | 70177281 | |||
chr16:70177296 | T | C | 9 | a0002 a0008 a0009 others(6): Show |
76 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(73): Show |
missense_variant | MODERATE | c.272T>C | p.Ile91Thr | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 543/1987 | 272/1341 | 91/446 | chr16 | 70177296 | |||
chr16:70177298 | C | G | 1 | a0025 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.274C>G | p.Pro92Ala | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 545/1987 | 274/1341 | 92/446 | chr16 | 70177298 | |||
chr16:70177304 | C | A | 1 | a0025 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.280C>A | p.Pro94Thr | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 551/1987 | 280/1341 | 94/446 | chr16 | 70177304 | |||
chr16:70177305 | C | G | 1 | a0025 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.281C>G | p.Pro94Arg | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 552/1987 | 281/1341 | 94/446 | chr16 | 70177305 | |||
chr16:70177308 | G | T | 1 | a0025 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.284G>T | p.Ser95Ile | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 555/1987 | 284/1341 | 95/446 | chr16 | 70177308 | |||
chr16:70177323 | T | C | 11 | a0002 a0004 a0008 others(8): Show |
104 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(101): Show |
missense_variant | MODERATE | c.299T>C | p.Leu100Pro | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 570/1987 | 299/1341 | 100/446 | chr16 | 70177323 | |||
chr16:70177377 | C | T | 1 | a0011 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.353C>T | p.Ala118Val | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 624/1987 | 353/1341 | 118/446 | chr16 | 70177377 | |||
chr16:70177467 | C | G | 9 | a0002 a0004 a0008 others(6): Show |
102 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(99): Show |
missense_variant | MODERATE | c.443C>G | p.Thr148Ser | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 714/1987 | 443/1341 | 148/446 | chr16 | 70177467 | |||
chr16:70177476 | C | T | 1 | a0015 | 1 | HG02148.hp2 | missense_variant | MODERATE | c.452C>T | p.Thr151Met | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 723/1987 | 452/1341 | 151/446 | chr16 | 70177476 | |||
chr16:70177479 | A | T | 1 | a0006 | 10 | HG00621.hp1 HG02071.hp1 HG02523.hp2 others(7): Show |
missense_variant&splice_region_variant | MODERATE | c.455A>T | p.Gln152Leu | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 726/1987 | 455/1341 | 152/446 | chr16 | 70177479 | |||
chr16:70181897 | C | G | 1 | a0021 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.504C>G | p.Cys168Trp | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 5/13 | 775/1987 | 504/1341 | 168/446 | chr16 | 70181897 | |||
chr16:70181907 | C | T | 1 | a0016 | 1 | HG02486.hp1 | stop_gained | HIGH | c.514C>T | p.Gln172* | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 5/13 | 785/1987 | 514/1341 | 172/446 | chr16 | 70181907 | |||
chr16:70181910 | G | A | 1 | a0007 | 9 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(6): Show |
missense_variant | MODERATE | c.517G>A | p.Ala173Thr | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 5/13 | 788/1987 | 517/1341 | 173/446 | chr16 | 70181910 | |||
chr16:70181914 | C | T | 10 | a0002 a0004 a0008 others(7): Show |
101 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(98): Show |
missense_variant | MODERATE | c.521C>T | p.Ala174Val | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 5/13 | 792/1987 | 521/1341 | 174/446 | chr16 | 70181914 | |||
chr16:70181946 | A | G | 19 | a0001 a0002 a0004 others(16): Show |
300 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(297): Show |
missense_variant&splice_region_variant | MODERATE | c.553A>G | p.Arg185Gly | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 5/13 | 824/1987 | 553/1341 | 185/446 | chr16 | 70181946 | |||
chr16:70182399 | G | A | 9 | a0001 a0005 a0006 others(6): Show |
199 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(196): Show |
missense_variant | MODERATE | c.586G>A | p.Val196Ile | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 6/13 | 857/1987 | 586/1341 | 196/446 | chr16 | 70182399 | |||
chr16:70183321 | G | C | 7 | a0004 a0008 a0009 others(4): Show |
38 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
missense_variant | MODERATE | c.825G>C | p.Glu275Asp | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 8/13 | 1096/1987 | 825/1341 | 275/446 | chr16 | 70183321 | |||
chr16:70183794 | G | A | 8 | a0004 a0008 a0009 others(5): Show |
39 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
missense_variant | MODERATE | c.919G>A | p.Asp307Asn | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/13 | 1190/1987 | 919/1341 | 307/446 | chr16 | 70183794 | |||
chr16:70183847 | G | C | 7 | a0004 a0008 a0009 others(4): Show |
38 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
missense_variant | MODERATE | c.972G>C | p.Arg324Ser | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/13 | 1243/1987 | 972/1341 | 324/446 | chr16 | 70183847 | |||
chr16:70184503 | G | A | 2 | a0005 a0006 |
27 | HG00140.hp1 HG00323.hp1 HG00621.hp1 others(24): Show |
missense_variant | MODERATE | c.994G>A | p.Gly332Arg | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/13 | 1265/1987 | 994/1341 | 332/446 | chr16 | 70184503 | |||
chr16:70184506 | G | T | 1 | a0026 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.997G>T | p.Val333Leu | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/13 | 1268/1987 | 997/1341 | 333/446 | chr16 | 70184506 | |||
chr16:70184507 | T | G | 1 | a0026 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.998T>G | p.Val333Gly | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/13 | 1269/1987 | 998/1341 | 333/446 | chr16 | 70184507 | |||
chr16:70184563 | C | T | 1 | a0018 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1054C>T | p.Arg352Cys | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/13 | 1325/1987 | 1054/1341 | 352/446 | chr16 | 70184563 | |||
chr16:70184572 | A | C | 1 | a0026 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.1063A>C | p.Thr355Pro | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/13 | 1334/1987 | 1063/1341 | 355/446 | chr16 | 70184572 | |||
chr16:70184923 | CCTT | C | 1 | a0009 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
conservative_inframe_deletion | MODERATE | c.1144_1146delTTC | p.Phe382del | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/13 | 1415/1987 | 1144/1341 | 382/446 | INFO_REALIGN_3_PRIME | chr16 | 70184923 | ||
chr16:70184959 | C | G | 3 | a0004 a0013 a0019 |
29 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(26): Show |
missense_variant | MODERATE | c.1178C>G | p.Thr393Ser | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/13 | 1449/1987 | 1178/1341 | 393/446 | chr16 | 70184959 | |||
chr16:70185934 | A | G | 14 | a0002 a0004 a0008 others(11): Show |
107 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(104): Show |
missense_variant | MODERATE | c.1261A>G | p.Asn421Asp | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 12/13 | 1532/1987 | 1261/1341 | 421/446 | chr16 | 70185934 | |||
chr16:70186488 | G | A | 1 | a0010 | 2 | HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.1309G>A | p.Glu437Lys | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 13/13 | 1580/1987 | 1309/1341 | 437/446 | chr16 | 70186488 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:70174392 | G | A | 1 | a0002c0011 | 2 | HG01255.hp2 HG01515.hp1 |
synonymous_variant | LOW | c.114G>A | p.Pro38Pro | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/13 | 385/1987 | 114/1341 | 38/446 | chr16 | 70174392 | |||
chr16:70175030 | C | A | 1 | a0004c0008 | 5 | HG02258.hp1 HG02559.hp1 HG02896.hp1 others(2): Show |
synonymous_variant | LOW | c.208C>A | p.Arg70Arg | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/13 | 479/1987 | 208/1341 | 70/446 | chr16 | 70175030 | |||
chr16:70177261 | C | A | 1 | a0025c0014 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.237C>A | p.Ala79Ala | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 508/1987 | 237/1341 | 79/446 | chr16 | 70177261 | |||
chr16:70177264 | A | G | 8 | a0004c0004 a0004c0008 a0004c0029 others(5): Show |
34 | HG00140.hp2 HG01433.hp1 HG01891.hp1 others(31): Show |
synonymous_variant | LOW | c.240A>G | p.Gln80Gln | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 511/1987 | 240/1341 | 80/446 | chr16 | 70177264 | |||
chr16:70177297 | C | A | 1 | a0025c0014 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.273C>A | p.Ile91Ile | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 544/1987 | 273/1341 | 91/446 | chr16 | 70177297 | |||
chr16:70177303 | C | T | 1 | a0025c0014 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.279C>T | p.Thr93Thr | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 550/1987 | 279/1341 | 93/446 | chr16 | 70177303 | |||
chr16:70177306 | G | A | 1 | a0025c0014 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.282G>A | p.Pro94Pro | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 553/1987 | 282/1341 | 94/446 | chr16 | 70177306 | |||
chr16:70177333 | C | A | 1 | a0025c0014 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.309C>A | p.Thr103Thr | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 580/1987 | 309/1341 | 103/446 | chr16 | 70177333 | |||
chr16:70177363 | G | A | 2 | a0011c0026 a0017c0025 |
2 | HG00140.hp2 HG02572.hp1 |
synonymous_variant | LOW | c.339G>A | p.Leu113Leu | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 610/1987 | 339/1341 | 113/446 | chr16 | 70177363 | |||
chr16:70177387 | T | C | 16 | a0002c0002 a0002c0011 a0004c0004 others(13): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
synonymous_variant | LOW | c.363T>C | p.Val121Val | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 634/1987 | 363/1341 | 121/446 | chr16 | 70177387 | |||
chr16:70177402 | A | G | 2 | a0007c0007 a0024c0013 |
10 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(7): Show |
synonymous_variant | LOW | c.378A>G | p.Leu126Leu | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 649/1987 | 378/1341 | 126/446 | chr16 | 70177402 | |||
chr16:70177477 | G | A | 12 | a0002c0002 a0002c0011 a0004c0004 others(9): Show |
102 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(99): Show |
synonymous_variant | LOW | c.453G>A | p.Thr151Thr | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/13 | 724/1987 | 453/1341 | 151/446 | chr16 | 70177477 | |||
chr16:70182651 | C | T | 1 | a0004c0029 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.681C>T | p.Val227Val | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/13 | 952/1987 | 681/1341 | 227/446 | chr16 | 70182651 | |||
chr16:70182687 | T | C | 6 | a0002c0002 a0002c0011 a0014c0016 others(3): Show |
67 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(64): Show |
synonymous_variant | LOW | c.717T>C | p.His239His | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/13 | 988/1987 | 717/1341 | 239/446 | chr16 | 70182687 | |||
chr16:70184571 | G | A | 1 | a0026c0017 | 1 | NA19003.hp1 | synonymous_variant | LOW | c.1062G>A | p.Glu354Glu | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/13 | 1333/1987 | 1062/1341 | 354/446 | chr16 | 70184571 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:70173795 | T | C | 6 | a0001c0001t0011 a0001c0001t0018 a0002c0011t0017 others(3): Show |
7 | HG01255.hp2 HG01515.hp2 HG01884.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-263T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/13 | 484 | chr16 | 70173795 | ||||||
chr16:70173820 | G | A | 2 | a0001c0001t0011 a0017c0025t0014 |
3 | HG01884.hp2 HG02572.hp1 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-238G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/13 | 459 | chr16 | 70173820 | ||||||
chr16:70173840 | C | T | 1 | a0012c0020t0022 | 1 | HG00639.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-218C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/13 | chr16 | 70173840 | |||||||
chr16:70173925 | T | C | 8 | a0002c0002t0002 a0002c0002t0012 a0002c0011t0002 others(5): Show |
66 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(63): Show |
5_prime_UTR_variant | MODIFIER | c.-133T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/13 | 354 | chr16 | 70173925 | ||||||
chr16:70173925 | T | G | 1 | a0002c0002t0019 | 1 | HG01169.hp2 | 5_prime_UTR_variant | MODIFIER | c.-133T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/13 | 354 | chr16 | 70173925 | ||||||
chr16:70173935 | G | C | 1 | a0024c0013t0015 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-123G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/13 | 344 | chr16 | 70173935 | ||||||
chr16:70173937 | A | G | 4 | a0001c0001t0011 a0001c0001t0018 a0002c0002t0012 others(1): Show |
6 | HG01884.hp2 HG02040.hp2 HG02135.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-121A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/13 | 342 | chr16 | 70173937 | ||||||
chr16:70173948 | C | T | 1 | a0002c0011t0017 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-110C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/13 | 331 | chr16 | 70173948 | ||||||
chr16:70174228 | G | A | 1 | a0001c0001t0020 | 1 | HG02040.hp1 | 5_prime_UTR_variant | MODIFIER | c.-51G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/13 | 51 | chr16 | 70174228 | ||||||
chr16:70174256 | T | C | 30 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0009 others(27): Show |
144 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(141): Show |
5_prime_UTR_variant | MODIFIER | c.-23T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/13 | 23 | chr16 | 70174256 | ||||||
chr16:70174264 | G | A | 2 | a0001c0001t0008 a0001c0001t0013 |
6 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-15G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/13 | 15 | chr16 | 70174264 | ||||||
chr16:70186543 | G | C | 16 | a0002c0002t0002 a0002c0002t0010 a0002c0002t0012 others(13): Show |
89 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*23G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 13/13 | 23 | chr16 | 70186543 | ||||||
chr16:70186578 | C | T | 21 | a0002c0002t0002 a0002c0002t0010 a0002c0002t0012 others(18): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*58C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 13/13 | 58 | chr16 | 70186578 | ||||||
chr16:70186612 | C | T | 4 | a0004c0004t0006 a0004c0029t0006 a0017c0025t0014 others(1): Show |
16 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*92C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 13/13 | 92 | chr16 | 70186612 | ||||||
chr16:70186623 | A | G | 1 | a0001c0001t0008 | 4 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*103A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 13/13 | 103 | chr16 | 70186623 | ||||||
chr16:70186725 | C | T | 10 | a0002c0002t0002 a0002c0002t0010 a0002c0002t0012 others(7): Show |
67 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*205C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 13/13 | 205 | chr16 | 70186725 | ||||||
chr16:70186747 | G | A | 1 | a0022c0015t0021 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*227G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 13/13 | 227 | chr16 | 70186747 | ||||||
chr16:70186771 | A | G | 29 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0018 others(26): Show |
188 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*251A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 13/13 | 251 | chr16 | 70186771 | ||||||
chr16:70186842 | G | A | 1 | a0001c0001t0018 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 13/13 | 322 | chr16 | 70186842 | ||||||
chr16:70186869 | A | G | 4 | a0004c0004t0006 a0004c0029t0006 a0017c0025t0014 others(1): Show |
16 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*349A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 13/13 | 349 | chr16 | 70186869 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:70174011 | T | G | 1 | a0024c0013t0015g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-107+60T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/12 | chr16 | 70174011 | |||||||
chr16:70174063 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-106-110C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/12 | chr16 | 70174063 | |||||||
chr16:70174083 | C | T | 1 | a0003c0003t0001g0194 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-106-90C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/12 | chr16 | 70174083 | |||||||
chr16:70174154 | T | TCCTTCTT others(14): Show |
1 | a0024c0013t0015g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-106-17_-106-16ins others(21): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 70174154 | ||||||
chr16:70174162 | T | C | 2 | a0001c0001t0001g0048 a0002c0011t0017g0047 |
2 | HG01255.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-106-11T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 1/12 | chr16 | 70174162 | |||||||
chr16:70174403 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03710.hp1 | splice_donor_variant&intron_variant | HIGH | c.124+1G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174403 | |||||||
chr16:70174444 | T | C | 99 | a0001c0001t0001g0085 a0001c0001t0003g0007 a0001c0001t0003g0008 others(96): Show |
162 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.124+42T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174444 | |||||||
chr16:70174488 | C | T | 1 | a0016c0018t0007g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.124+86C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174488 | |||||||
chr16:70174512 | C | T | 5 | a0008c0009t0007g0120 a0008c0009t0007g0121 a0008c0009t0007g0123 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+110C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174512 | |||||||
chr16:70174513 | G | C | 1 | a0005c0005t0001g0125 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.124+111G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174513 | |||||||
chr16:70174551 | C | T | 1 | a0003c0003t0001g0045 | 2 | NA18954.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.124+149C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174551 | |||||||
chr16:70174552 | G | A | 3 | a0001c0001t0003g0007 a0001c0001t0003g0050 a0001c0001t0003g0051 |
8 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+150G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174552 | |||||||
chr16:70174575 | G | GGGAGGAA others(3): Show |
7 | a0001c0001t0001g0044 a0001c0001t0004g0119 a0007c0007t0004g0013 others(4): Show |
12 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.124+187_124+196dup others(10): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 70174575 | ||||||
chr16:70174600 | C | T | 1 | a0004c0004t0005g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+198C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174600 | |||||||
chr16:70174630 | A | G | 37 | a0001c0001t0001g0187 a0002c0002t0002g0100 a0003c0003t0001g0190 others(34): Show |
45 | HG00140.hp2 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.124+228A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174630 | |||||||
chr16:70174655 | A | AC | 76 | a0001c0001t0001g0032 a0001c0001t0001g0127 a0001c0001t0003g0008 others(73): Show |
119 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.124+253_124+254ins others(1): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174655 | |||||||
chr16:70174698 | A | G | 30 | a0001c0001t0001g0186 a0002c0002t0002g0075 a0002c0002t0002g0076 others(27): Show |
38 | HG00323.hp2 HG00741.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.125-249A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174698 | |||||||
chr16:70174739 | C | T | 1 | a0004c0004t0006g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.125-208C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174739 | |||||||
chr16:70174748 | A | G | 1 | a0001c0001t0003g0093 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.125-199A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174748 | |||||||
chr16:70174937 | T | C | 85 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0129 others(82): Show |
126 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.125-10T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 2/12 | chr16 | 70174937 | |||||||
chr16:70175085 | C | T | 51 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0054 others(48): Show |
81 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.216+47C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175085 | |||||||
chr16:70175086 | G | T | 1 | a0002c0002t0002g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.216+48G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175086 | |||||||
chr16:70175147 | G | A | 1 | a0002c0011t0017g0047 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.216+109G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175147 | |||||||
chr16:70175174 | C | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(150): Show |
271 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.216+136C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175174 | |||||||
chr16:70175215 | G | A | 1 | a0011c0026t0009g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.216+177G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175215 | |||||||
chr16:70175311 | C | T | 6 | a0001c0001t0004g0091 a0001c0001t0004g0092 a0002c0002t0002g0070 others(3): Show |
6 | HG00140.hp2 HG01255.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+273C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175311 | |||||||
chr16:70175380 | C | G | 2 | a0005c0005t0001g0185 a0005c0005t0009g0090 |
2 | HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.216+342C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175380 | |||||||
chr16:70175393 | C | G | 2 | a0005c0005t0001g0035 a0005c0005t0001g0138 |
3 | HG00323.hp1 HG02258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.216+355C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175393 | |||||||
chr16:70175436 | G | A | 31 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(28): Show |
59 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.216+398G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175436 | |||||||
chr16:70175446 | C | T | 9 | a0001c0001t0001g0184 a0001c0001t0003g0042 a0001c0001t0003g0133 others(6): Show |
12 | HG00323.hp1 HG01109.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.216+408C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175446 | |||||||
chr16:70175488 | G | T | 35 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(32): Show |
71 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.216+450G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175488 | |||||||
chr16:70175557 | G | A | 41 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(38): Show |
78 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.216+519G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175557 | |||||||
chr16:70175568 | G | C | 1 | a0003c0003t0001g0017 | 4 | NA18946.hp1 NA18979.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+530G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175568 | |||||||
chr16:70175575 | G | A | 38 | a0001c0001t0003g0019 a0001c0001t0003g0093 a0002c0002t0002g0002 others(35): Show |
67 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.216+537G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175575 | |||||||
chr16:70175601 | C | T | 1 | a0013c0027t0005g0115 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.216+563C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175601 | |||||||
chr16:70175641 | C | A | 30 | a0002c0002t0002g0024 a0004c0004t0005g0016 a0004c0004t0005g0106 others(27): Show |
39 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.216+603C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175641 | |||||||
chr16:70175642 | T | C | 73 | a0001c0001t0001g0141 a0001c0001t0001g0186 a0001c0001t0004g0119 others(70): Show |
110 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.216+604T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175642 | |||||||
chr16:70175645 | A | C | 73 | a0001c0001t0001g0141 a0001c0001t0001g0186 a0001c0001t0004g0119 others(70): Show |
110 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.216+607A>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175645 | |||||||
chr16:70175656 | C | A | 31 | a0002c0002t0002g0024 a0004c0004t0005g0016 a0004c0004t0005g0106 others(28): Show |
40 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.216+618C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175656 | |||||||
chr16:70175760 | T | C | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.216+722T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175760 | |||||||
chr16:70175767 | A | G | 72 | a0001c0001t0001g0137 a0001c0001t0001g0181 a0002c0002t0002g0002 others(69): Show |
108 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.216+729A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175767 | |||||||
chr16:70175772 | C | T | 1 | a0017c0025t0014g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.216+734C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175772 | |||||||
chr16:70175773 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.216+735G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175773 | |||||||
chr16:70175781 | G | A | 6 | a0007c0007t0004g0013 a0007c0007t0004g0126 a0007c0007t0004g0191 others(3): Show |
10 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.216+743G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175781 | |||||||
chr16:70175803 | G | A | 27 | a0002c0011t0017g0047 a0004c0004t0005g0016 a0004c0004t0005g0106 others(24): Show |
33 | HG01255.hp2 HG01433.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.216+765G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175803 | |||||||
chr16:70175814 | T | G | 1 | a0002c0002t0002g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.216+776T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175814 | |||||||
chr16:70175815 | G | T | 1 | a0002c0002t0002g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.216+777G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175815 | |||||||
chr16:70175837 | C | T | 1 | a0004c0004t0006g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.216+799C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175837 | |||||||
chr16:70175848 | C | G | 1 | a0011c0026t0009g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.216+810C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70175848 | |||||||
chr16:70176020 | T | C | 69 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(66): Show |
105 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.216+982T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176020 | |||||||
chr16:70176038 | A | G | 69 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(66): Show |
105 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.216+1000A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176038 | |||||||
chr16:70176090 | G | A | 1 | a0003c0003t0001g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.216+1052G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176090 | |||||||
chr16:70176127 | T | C | 71 | a0001c0001t0001g0037 a0001c0001t0001g0134 a0002c0002t0002g0002 others(68): Show |
108 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.216+1089T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176127 | |||||||
chr16:70176167 | G | A | 66 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(63): Show |
102 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.217-1074G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176167 | |||||||
chr16:70176233 | C | T | 11 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0111 others(8): Show |
13 | HG01433.hp1 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.217-1008C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176233 | |||||||
chr16:70176278 | C | A | 1 | a0002c0002t0002g0055 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.217-963C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176278 | |||||||
chr16:70176297 | C | A | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.217-944C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176297 | |||||||
chr16:70176306 | A | T | 6 | a0007c0007t0004g0013 a0007c0007t0004g0126 a0007c0007t0004g0191 others(3): Show |
10 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.217-935A>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176306 | |||||||
chr16:70176423 | CA | C | 6 | a0007c0007t0004g0013 a0007c0007t0004g0126 a0007c0007t0004g0191 others(3): Show |
10 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.217-817delA | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176423 | |||||||
chr16:70176528 | G | C | 6 | a0007c0007t0004g0013 a0007c0007t0004g0126 a0007c0007t0004g0191 others(3): Show |
10 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.217-713G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176528 | |||||||
chr16:70176557 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.217-684C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176557 | |||||||
chr16:70176558 | G | A | 1 | a0002c0002t0002g0056 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.217-683G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176558 | |||||||
chr16:70176589 | T | C | 7 | a0001c0001t0003g0086 a0004c0004t0005g0016 a0004c0008t0005g0016 others(4): Show |
9 | HG00140.hp2 HG00738.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-652T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176589 | |||||||
chr16:70176616 | C | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0092 |
3 | NA18960.hp1 NA19007.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.217-625C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176616 | |||||||
chr16:70176620 | T | C | 1 | a0014c0016t0010g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.217-621T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176620 | |||||||
chr16:70176683 | T | G | 2 | a0010c0012t0001g0188 a0010c0012t0001g0189 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.217-558T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176683 | |||||||
chr16:70176708 | G | A | 1 | a0005c0005t0009g0090 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.217-533G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176708 | |||||||
chr16:70176719 | ACT | A | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.217-519_217-518del others(2): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 70176719 | ||||||
chr16:70176722 | C | T | 2 | a0001c0001t0003g0139 a0001c0001t0018g0182 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.217-519C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176722 | |||||||
chr16:70176728 | C | CA | 6 | a0007c0007t0004g0013 a0007c0007t0004g0126 a0007c0007t0004g0191 others(3): Show |
10 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.217-502dupA | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 70176728 | ||||||
chr16:70176728 | C | CAAAAAA | 10 | a0002c0002t0002g0054 a0002c0002t0002g0066 a0002c0002t0002g0078 others(7): Show |
10 | HG00323.hp2 HG01081.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.217-507_217-502dup others(6): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 70176728 | ||||||
chr16:70176728 | C | CAAAAAAA | 35 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(32): Show |
65 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.217-508_217-502dup others(7): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 70176728 | ||||||
chr16:70176728 | C | CAAAAAAA others(1): Show |
9 | a0002c0002t0002g0057 a0002c0002t0002g0079 a0004c0004t0005g0016 others(6): Show |
11 | HG02055.hp1 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.217-509_217-502dup others(8): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 70176728 | ||||||
chr16:70176728 | C | CAAAAAAA others(3): Show |
7 | a0004c0004t0006g0015 a0004c0004t0006g0031 a0004c0004t0006g0097 others(4): Show |
11 | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.217-511_217-502dup others(10): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 70176728 | ||||||
chr16:70176728 | C | CAAAAAAA others(4): Show |
3 | a0004c0004t0006g0096 a0004c0004t0006g0116 a0019c0028t0006g0103 |
3 | HG03098.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.217-512_217-502dup others(11): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 70176728 | ||||||
chr16:70176728 | C | CAAAAAAA others(7): Show |
1 | a0014c0016t0010g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.217-502_217-501ins others(14): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 70176728 | ||||||
chr16:70176755 | G | A | 37 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(34): Show |
65 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.217-486G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176755 | |||||||
chr16:70176758 | G | A | 6 | a0002c0002t0002g0075 a0002c0002t0002g0076 a0002c0002t0002g0078 others(3): Show |
6 | HG00323.hp2 HG00741.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-483G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176758 | |||||||
chr16:70176768 | C | T | 38 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(35): Show |
66 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.217-473C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176768 | |||||||
chr16:70176791 | A | G | 72 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(69): Show |
108 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.217-450A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176791 | |||||||
chr16:70176801 | G | A | 1 | a0011c0026t0009g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.217-440G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176801 | |||||||
chr16:70176823 | G | C | 2 | a0001c0001t0003g0050 a0001c0001t0003g0051 |
2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.217-418G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176823 | |||||||
chr16:70176825 | C | T | 42 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(39): Show |
81 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.217-416C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176825 | |||||||
chr16:70176867 | C | T | 1 | a0006c0006t0001g0041 | 2 | NA19083.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.217-374C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176867 | |||||||
chr16:70176943 | C | T | 37 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(34): Show |
65 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.217-298C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176943 | |||||||
chr16:70176986 | C | T | 1 | a0011c0026t0009g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.217-255C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176986 | |||||||
chr16:70176987 | T | G | 1 | a0002c0002t0002g0055 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.217-254T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70176987 | |||||||
chr16:70177000 | C | A | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.217-241C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70177000 | |||||||
chr16:70177014 | C | A | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.217-227C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70177014 | |||||||
chr16:70177043 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0146 a0001c0001t0001g0147 |
4 | NA18976.hp1 NA18983.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-198G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70177043 | |||||||
chr16:70177063 | C | T | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.217-178C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70177063 | |||||||
chr16:70177107 | T | C | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.217-134T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70177107 | |||||||
chr16:70177108 | C | T | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.217-133C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70177108 | |||||||
chr16:70177193 | C | CCACTTTG others(8): Show |
1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.217-47_217-46insAC others(13): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 70177193 | ||||||
chr16:70177204 | A | T | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.217-37A>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70177204 | |||||||
chr16:70177214 | A | T | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.217-27A>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70177214 | |||||||
chr16:70177221 | T | A | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.217-20T>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70177221 | |||||||
chr16:70177222 | C | G | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.217-19C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70177222 | |||||||
chr16:70177226 | T | A | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.217-15T>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 3/12 | chr16 | 70177226 | |||||||
chr16:70177506 | C | T | 3 | a0011c0026t0009g0117 a0014c0016t0010g0145 a0017c0025t0014g0108 |
3 | HG00140.hp2 HG01943.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.456+26C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177506 | |||||||
chr16:70177517 | C | T | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.456+37C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177517 | |||||||
chr16:70177538 | T | G | 76 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(73): Show |
116 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.456+58T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177538 | |||||||
chr16:70177608 | C | CT | 68 | a0001c0001t0001g0177 a0001c0001t0008g0012 a0001c0001t0009g0131 others(65): Show |
107 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.456+141dupT | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70177608 | ||||||
chr16:70177638 | G | C | 71 | a0001c0001t0001g0148 a0002c0002t0002g0002 a0002c0002t0002g0010 others(68): Show |
107 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.456+158G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177638 | |||||||
chr16:70177643 | G | T | 1 | a0001c0001t0003g0029 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.456+163G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177643 | |||||||
chr16:70177645 | G | C | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.456+165G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177645 | |||||||
chr16:70177656 | T | G | 1 | a0002c0002t0002g0075 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.456+176T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177656 | |||||||
chr16:70177670 | C | G | 24 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0109 others(21): Show |
32 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.456+190C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177670 | |||||||
chr16:70177699 | A | G | 76 | a0001c0001t0003g0008 a0002c0002t0002g0002 a0002c0002t0002g0010 others(73): Show |
116 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.456+219A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177699 | |||||||
chr16:70177716 | A | C | 1 | a0017c0025t0014g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.456+236A>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177716 | |||||||
chr16:70177794 | T | C | 2 | a0003c0003t0001g0140 a0003c0003t0001g0149 |
2 | HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.456+314T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177794 | |||||||
chr16:70177795 | A | G | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.456+315A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177795 | |||||||
chr16:70177815 | A | C | 67 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(64): Show |
103 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.456+335A>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177815 | |||||||
chr16:70177862 | T | C | 1 | a0024c0013t0015g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.456+382T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177862 | |||||||
chr16:70177864 | C | A | 1 | a0024c0013t0015g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.456+384C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177864 | |||||||
chr16:70177870 | T | G | 1 | a0002c0002t0002g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.456+390T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177870 | |||||||
chr16:70177886 | G | A | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.456+406G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177886 | |||||||
chr16:70177896 | G | T | 1 | a0024c0013t0015g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.456+416G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177896 | |||||||
chr16:70177938 | G | C | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.456+458G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177938 | |||||||
chr16:70177967 | C | T | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.456+487C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177967 | |||||||
chr16:70177980 | T | C | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.456+500T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70177980 | |||||||
chr16:70178058 | C | A | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.456+578C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178058 | |||||||
chr16:70178059 | T | A | 69 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(66): Show |
105 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.456+579T>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178059 | |||||||
chr16:70178059 | T | C | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.456+579T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178059 | |||||||
chr16:70178060 | C | T | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.456+580C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178060 | |||||||
chr16:70178061 | T | A | 1 | a0025c0014t0002g0065 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.456+581T>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178061 | |||||||
chr16:70178067 | C | CAGCTCAT others(20): Show |
1 | a0003c0003t0001g0194 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.456+588_456+614dup others(27): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70178067 | ||||||
chr16:70178070 | CTCATTTT others(9): Show |
C | 1 | a0002c0002t0002g0064 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.456+592_456+607del others(16): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70178070 | ||||||
chr16:70178116 | C | T | 3 | a0011c0026t0009g0117 a0014c0016t0010g0145 a0017c0025t0014g0108 |
3 | HG00140.hp2 HG01943.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.456+636C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178116 | |||||||
chr16:70178126 | C | A | 1 | a0002c0002t0002g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.456+646C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178126 | |||||||
chr16:70178146 | T | C | 67 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(64): Show |
103 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.456+666T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178146 | |||||||
chr16:70178147 | G | T | 1 | a0002c0002t0002g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.456+667G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178147 | |||||||
chr16:70178180 | G | A | 34 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0109 others(31): Show |
42 | HG00140.hp2 HG01433.hp1 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.456+700G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178180 | |||||||
chr16:70178255 | A | G | 57 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(54): Show |
91 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.456+775A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178255 | |||||||
chr16:70178280 | G | A | 1 | a0011c0026t0009g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.456+800G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178280 | |||||||
chr16:70178357 | G | A | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.456+877G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178357 | |||||||
chr16:70178390 | A | G | 76 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(73): Show |
116 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.456+910A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178390 | |||||||
chr16:70178460 | T | C | 3 | a0001c0001t0001g0150 a0011c0026t0009g0117 a0017c0025t0014g0108 |
3 | HG00140.hp2 HG02572.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.456+980T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178460 | |||||||
chr16:70178507 | G | C | 3 | a0011c0026t0009g0117 a0013c0027t0005g0115 a0017c0025t0014g0108 |
3 | HG00140.hp2 HG01433.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.456+1027G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178507 | |||||||
chr16:70178534 | A | G | 1 | a0011c0026t0009g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.456+1054A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178534 | |||||||
chr16:70178564 | G | A | 6 | a0007c0007t0004g0013 a0007c0007t0004g0126 a0007c0007t0004g0191 others(3): Show |
10 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.456+1084G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178564 | |||||||
chr16:70178575 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA18976.hp1 | intron_variant | MODIFIER | c.456+1095A>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178575 | |||||||
chr16:70178576 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA18976.hp1 | intron_variant | MODIFIER | c.456+1096C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178576 | |||||||
chr16:70178578 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18976.hp1 | intron_variant | MODIFIER | c.456+1098G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178578 | |||||||
chr16:70178689 | C | CTGAT | 39 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(36): Show |
67 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.456+1209_456+1210i others(6): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178689 | |||||||
chr16:70178731 | A | G | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.456+1251A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178731 | |||||||
chr16:70178737 | T | C | 1 | a0005c0005t0001g0151 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.456+1257T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178737 | |||||||
chr16:70178765 | T | C | 41 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(38): Show |
69 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.456+1285T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178765 | |||||||
chr16:70178822 | C | T | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.456+1342C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178822 | |||||||
chr16:70178839 | G | T | 1 | a0003c0003t0001g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.456+1359G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178839 | |||||||
chr16:70178875 | C | A | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.456+1395C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178875 | |||||||
chr16:70178876 | G | A | 1 | a0002c0002t0002g0059 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.456+1396G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178876 | |||||||
chr16:70178892 | A | T | 1 | a0014c0016t0010g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.456+1412A>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178892 | |||||||
chr16:70178894 | T | A | 1 | a0014c0016t0010g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.456+1414T>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178894 | |||||||
chr16:70178895 | C | T | 1 | a0014c0016t0010g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.456+1415C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178895 | |||||||
chr16:70178950 | C | T | 40 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(37): Show |
68 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.456+1470C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178950 | |||||||
chr16:70178968 | A | C | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.456+1488A>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178968 | |||||||
chr16:70178985 | A | C | 3 | a0003c0003t0001g0045 a0003c0003t0001g0175 a0003c0003t0009g0174 |
4 | HG00597.hp1 NA18954.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+1505A>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178985 | |||||||
chr16:70178993 | A | G | 30 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0109 others(27): Show |
38 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.456+1513A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70178993 | |||||||
chr16:70179082 | A | G | 39 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(36): Show |
67 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.456+1602A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179082 | |||||||
chr16:70179149 | T | C | 114 | a0001c0001t0001g0135 a0001c0001t0003g0007 a0001c0001t0003g0008 others(111): Show |
189 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.456+1669T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179149 | |||||||
chr16:70179234 | C | A | 1 | a0002c0002t0019g0068 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.456+1754C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179234 | |||||||
chr16:70179260 | A | AT | 41 | a0001c0001t0001g0135 a0002c0002t0002g0002 a0002c0002t0002g0010 others(38): Show |
71 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.456+1797dupT | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70179260 | ||||||
chr16:70179260 | A | ATT | 16 | a0002c0002t0002g0055 a0002c0002t0002g0063 a0002c0002t0002g0094 others(13): Show |
20 | HG01123.hp2 HG01169.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.456+1796_456+1797d others(4): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70179260 | ||||||
chr16:70179260 | AT | A | 16 | a0001c0001t0001g0039 a0001c0001t0001g0152 a0001c0001t0001g0195 others(13): Show |
21 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.456+1797delT | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70179260 | ||||||
chr16:70179290 | T | C | 7 | a0001c0001t0001g0135 a0001c0001t0003g0139 a0007c0007t0004g0013 others(4): Show |
11 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.456+1810T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179290 | |||||||
chr16:70179300 | C | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02523.hp1 NA19000.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.456+1820C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179300 | |||||||
chr16:70179308 | A | G | 8 | a0001c0001t0001g0135 a0001c0001t0003g0139 a0007c0007t0004g0013 others(5): Show |
12 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.456+1828A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179308 | |||||||
chr16:70179320 | C | T | 43 | a0001c0001t0001g0135 a0001c0001t0003g0007 a0001c0001t0003g0008 others(40): Show |
82 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.456+1840C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179320 | |||||||
chr16:70179323 | G | A | 1 | a0015c0023t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.456+1843G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179323 | |||||||
chr16:70179423 | T | C | 133 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0038 others(130): Show |
223 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.456+1943T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179423 | |||||||
chr16:70179504 | C | T | 1 | a0011c0026t0009g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.456+2024C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179504 | |||||||
chr16:70179511 | C | T | 68 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(65): Show |
102 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.456+2031C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179511 | |||||||
chr16:70179513 | C | T | 1 | a0011c0026t0009g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.456+2033C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179513 | |||||||
chr16:70179541 | T | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(110): Show |
202 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.456+2061T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179541 | |||||||
chr16:70179579 | G | C | 1 | a0009c0010t0005g0020 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.456+2099G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179579 | |||||||
chr16:70179609 | C | G | 3 | a0004c0004t0006g0031 a0004c0004t0006g0105 a0004c0029t0006g0104 |
4 | HG01891.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+2129C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179609 | |||||||
chr16:70179620 | T | G | 1 | a0002c0002t0002g0064 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.456+2140T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179620 | |||||||
chr16:70179674 | T | G | 1 | a0024c0013t0015g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.457-2176T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179674 | |||||||
chr16:70179675 | C | T | 1 | a0024c0013t0015g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.457-2175C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179675 | |||||||
chr16:70179676 | T | C | 1 | a0024c0013t0015g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.457-2174T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179676 | |||||||
chr16:70179835 | T | G | 76 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(73): Show |
116 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.457-2015T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179835 | |||||||
chr16:70179953 | A | C | 71 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(68): Show |
107 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.457-1897A>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179953 | |||||||
chr16:70179964 | A | T | 76 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(73): Show |
116 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.457-1886A>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70179964 | |||||||
chr16:70180043 | G | GT | 68 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(65): Show |
104 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.457-1801dupT | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70180043 | ||||||
chr16:70180106 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0004g0092 |
3 | NA18960.hp1 NA19007.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.457-1744G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180106 | |||||||
chr16:70180109 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.457-1741C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180109 | |||||||
chr16:70180153 | A | G | 1 | a0001c0001t0003g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.457-1697A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180153 | |||||||
chr16:70180153 | A | T | 72 | a0001c0001t0018g0182 a0002c0002t0002g0002 a0002c0002t0002g0010 others(69): Show |
108 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.457-1697A>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180153 | |||||||
chr16:70180307 | T | G | 1 | a0011c0026t0009g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.457-1543T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180307 | |||||||
chr16:70180327 | A | AAAGTGCT others(20): Show |
1 | a0014c0016t0010g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.457-1505_457-1504i others(29): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70180327 | ||||||
chr16:70180483 | G | C | 71 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(68): Show |
107 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.457-1367G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180483 | |||||||
chr16:70180540 | A | G | 69 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(66): Show |
105 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.457-1310A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180540 | |||||||
chr16:70180586 | C | T | 5 | a0007c0007t0004g0013 a0007c0007t0004g0126 a0007c0007t0004g0191 others(2): Show |
9 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.457-1264C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180586 | |||||||
chr16:70180587 | G | T | 1 | a0016c0018t0007g0122 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.457-1263G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180587 | |||||||
chr16:70180624 | T | A | 1 | a0002c0002t0002g0061 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.457-1226T>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180624 | |||||||
chr16:70180937 | C | G | 1 | a0022c0015t0021g0102 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.457-913C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180937 | |||||||
chr16:70180959 | G | C | 1 | a0002c0002t0002g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.457-891G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70180959 | |||||||
chr16:70181212 | G | A | 5 | a0007c0007t0004g0013 a0007c0007t0004g0126 a0007c0007t0004g0191 others(2): Show |
9 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.457-638G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181212 | |||||||
chr16:70181213 | G | C | 5 | a0007c0007t0004g0013 a0007c0007t0004g0126 a0007c0007t0004g0191 others(2): Show |
9 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.457-637G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181213 | |||||||
chr16:70181262 | T | A | 1 | a0001c0001t0003g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.457-588T>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181262 | |||||||
chr16:70181262 | T | C | 5 | a0007c0007t0004g0013 a0007c0007t0004g0126 a0007c0007t0004g0191 others(2): Show |
9 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.457-588T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181262 | |||||||
chr16:70181304 | A | G | 1 | a0003c0003t0001g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.457-546A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181304 | |||||||
chr16:70181316 | T | G | 68 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(65): Show |
102 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.457-534T>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181316 | |||||||
chr16:70181369 | C | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(90): Show |
167 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.457-481C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181369 | |||||||
chr16:70181437 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
199 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.457-413T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181437 | |||||||
chr16:70181472 | G | C | 1 | a0024c0013t0015g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.457-378G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181472 | |||||||
chr16:70181480 | G | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(142): Show |
242 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.457-370G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181480 | |||||||
chr16:70181508 | G | GGCATGGG others(8): Show |
1 | a0006c0006t0001g0161 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.457-340_457-339ins others(15): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181508 | ||||||
chr16:70181508 | G | GGCATGGT others(7): Show |
78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(75): Show |
133 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.457-340_457-339ins others(14): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181508 | ||||||
chr16:70181508 | G | GGCATGGT others(7): Show |
66 | a0001c0001t0001g0160 a0001c0001t0003g0007 a0001c0001t0003g0008 others(63): Show |
108 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.457-340_457-339ins others(14): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181508 | ||||||
chr16:70181565 | G | A | 1 | a0009c0010t0005g0020 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.457-285G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181565 | |||||||
chr16:70181575 | G | A | 1 | a0009c0010t0005g0020 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.457-275G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181575 | |||||||
chr16:70181620 | G | T | 1 | a0002c0002t0002g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.457-230G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181620 | |||||||
chr16:70181638 | A | AAAAT | 10 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0134 others(7): Show |
24 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.457-177_457-174dup others(4): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181638 | ||||||
chr16:70181638 | A | AAAATAAA others(1): Show |
5 | a0001c0001t0001g0038 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
6 | HG02523.hp1 NA18612.hp2 NA18976.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-181_457-174dup others(8): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181638 | ||||||
chr16:70181638 | AAAAT | A | 35 | a0003c0003t0001g0001 a0003c0003t0001g0017 a0003c0003t0001g0034 others(32): Show |
65 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.457-177_457-174del others(4): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181638 | ||||||
chr16:70181638 | AAAATAAA others(1): Show |
A | 49 | a0001c0001t0003g0009 a0001c0001t0003g0128 a0001c0001t0003g0132 others(46): Show |
85 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.457-181_457-174del others(8): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181638 | ||||||
chr16:70181638 | AAAATAAA others(5): Show |
A | 5 | a0008c0009t0007g0120 a0008c0009t0007g0121 a0008c0009t0007g0123 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.457-185_457-174del others(12): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181638 | ||||||
chr16:70181674 | T | TAAAA | 12 | a0001c0001t0003g0008 a0001c0001t0003g0025 a0001c0001t0003g0073 others(9): Show |
26 | HG00408.hp1 HG00544.hp1 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.457-174_457-173ins others(4): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181674 | ||||||
chr16:70181674 | T | TAAATAAA others(1): Show |
32 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0032 others(29): Show |
56 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.457-174_457-173ins others(8): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181674 | ||||||
chr16:70181674 | T | TAAATAAA others(5): Show |
32 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0039 others(29): Show |
56 | HG00140.hp1 HG00621.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.457-174_457-173ins others(12): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181674 | ||||||
chr16:70181674 | T | TAAATAAA others(9): Show |
12 | a0001c0001t0001g0130 a0001c0001t0003g0139 a0005c0005t0001g0138 others(9): Show |
18 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.457-174_457-173ins others(16): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181674 | ||||||
chr16:70181674 | T | TAAATAAA others(13): Show |
1 | a0001c0001t0001g0165 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.457-174_457-173ins others(20): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 70181674 | ||||||
chr16:70181677 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.457-173G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181677 | |||||||
chr16:70181678 | C | G | 3 | a0004c0004t0006g0031 a0004c0004t0006g0105 a0004c0029t0006g0104 |
4 | HG01891.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.457-172C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181678 | |||||||
chr16:70181741 | C | G | 66 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(63): Show |
100 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.457-109C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181741 | |||||||
chr16:70181746 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
199 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.457-104G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181746 | |||||||
chr16:70181768 | C | G | 45 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(42): Show |
73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.457-82C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181768 | |||||||
chr16:70181769 | A | G | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(164): Show |
285 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(282): Show |
intron_variant | MODIFIER | c.457-81A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181769 | |||||||
chr16:70181800 | C | T | 1 | a0002c0002t0002g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.457-50C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181800 | |||||||
chr16:70181803 | C | A | 1 | a0024c0013t0015g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.457-47C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181803 | |||||||
chr16:70181804 | A | G | 1 | a0024c0013t0015g0046 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.457-46A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181804 | |||||||
chr16:70181834 | CCT | C | 45 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(42): Show |
73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.457-15_457-14delCT | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 4/12 | chr16 | 70181834 | |||||||
chr16:70181965 | C | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(106): Show |
197 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.554+18C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 5/12 | chr16 | 70181965 | |||||||
chr16:70182140 | C | T | 1 | a0004c0004t0005g0109 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.554+193C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 5/12 | chr16 | 70182140 | |||||||
chr16:70182288 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(107): Show |
198 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.555-80G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 5/12 | chr16 | 70182288 | |||||||
chr16:70182291 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(107): Show |
198 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.555-77C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 5/12 | chr16 | 70182291 | |||||||
chr16:70182310 | T | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
199 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.555-58T>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 5/12 | chr16 | 70182310 | |||||||
chr16:70182582 | G | C | 1 | a0001c0001t0003g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.677-65G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 6/12 | chr16 | 70182582 | |||||||
chr16:70182586 | GC | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
199 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.677-60delC | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 6/12 | chr16 | 70182586 | |||||||
chr16:70182599 | C | A | 1 | a0001c0001t0001g0187 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.677-48C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 6/12 | chr16 | 70182599 | |||||||
chr16:70182610 | A | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(109): Show |
202 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.677-37A>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 6/12 | chr16 | 70182610 | |||||||
chr16:70182631 | C | T | 1 | a0009c0010t0005g0020 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.677-16C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 6/12 | chr16 | 70182631 | |||||||
chr16:70182643 | C | T | 1 | a0004c0029t0006g0104 | 1 | HG02965.hp1 | splice_region_variant&intron_variant | LOW | c.677-4C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 6/12 | chr16 | 70182643 | |||||||
chr16:70182884 | A | G | 2 | a0010c0012t0001g0188 a0010c0012t0001g0189 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.784+130A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | chr16 | 70182884 | |||||||
chr16:70182906 | C | G | 37 | a0001c0001t0003g0139 a0002c0002t0002g0010 a0002c0002t0002g0058 others(34): Show |
49 | HG01070.hp1 HG01346.hp1 HG01433.hp1 others(46): Show |
intron_variant | MODIFIER | c.784+152C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | chr16 | 70182906 | |||||||
chr16:70182926 | A | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(111): Show |
203 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.784+172A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | chr16 | 70182926 | |||||||
chr16:70182959 | A | G | 38 | a0002c0002t0002g0010 a0002c0002t0002g0058 a0002c0002t0002g0059 others(35): Show |
50 | HG01070.hp1 HG01346.hp1 HG01433.hp1 others(47): Show |
intron_variant | MODIFIER | c.784+205A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | chr16 | 70182959 | |||||||
chr16:70183056 | C | A | 31 | a0002c0002t0002g0002 a0002c0002t0002g0024 a0002c0002t0002g0053 others(28): Show |
55 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.785-225C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | chr16 | 70183056 | |||||||
chr16:70183127 | C | A | 8 | a0001c0001t0004g0005 a0001c0001t0004g0014 a0001c0001t0004g0026 others(5): Show |
20 | HG00544.hp2 HG02015.hp2 HG03239.hp1 others(17): Show |
intron_variant | MODIFIER | c.785-154C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | chr16 | 70183127 | |||||||
chr16:70183163 | A | C | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(172): Show |
293 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.785-118A>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | chr16 | 70183163 | |||||||
chr16:70183212 | C | CT | 30 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0109 others(27): Show |
38 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.785-68dupT | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr16 | 70183212 | ||||||
chr16:70183214 | C | T | 30 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0109 others(27): Show |
38 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.785-67C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | chr16 | 70183214 | |||||||
chr16:70183226 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.785-55G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | chr16 | 70183226 | |||||||
chr16:70183229 | G | A | 30 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0109 others(27): Show |
38 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.785-52G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | chr16 | 70183229 | |||||||
chr16:70183262 | C | T | 30 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0109 others(27): Show |
38 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.785-19C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 7/12 | chr16 | 70183262 | |||||||
chr16:70183500 | T | A | 1 | a0003c0003t0001g0167 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.877+127T>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 8/12 | chr16 | 70183500 | |||||||
chr16:70183555 | A | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0129 others(1): Show |
6 | NA18966.hp1 NA18974.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+182A>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 8/12 | chr16 | 70183555 | |||||||
chr16:70183564 | AT | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(147): Show |
267 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.878-178delT | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 70183564 | ||||||
chr16:70183564 | ATTT | A | 29 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0109 others(26): Show |
35 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.878-180_878-178del others(3): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 70183564 | ||||||
chr16:70183618 | G | A | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.878-135G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 8/12 | chr16 | 70183618 | |||||||
chr16:70183634 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0011g0028 |
3 | HG01884.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.878-119A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 8/12 | chr16 | 70183634 | |||||||
chr16:70183716 | T | C | 39 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(36): Show |
67 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.878-37T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 8/12 | chr16 | 70183716 | |||||||
chr16:70183864 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19000.hp2 | splice_region_variant&intron_variant | LOW | c.984+5C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70183864 | |||||||
chr16:70183868 | C | T | 30 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0109 others(27): Show |
38 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.984+9C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70183868 | |||||||
chr16:70183887 | A | G | 39 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(36): Show |
67 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.984+28A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70183887 | |||||||
chr16:70183889 | C | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(111): Show |
203 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.984+30C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70183889 | |||||||
chr16:70183904 | G | T | 38 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(35): Show |
66 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.984+45G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70183904 | |||||||
chr16:70183907 | A | T | 7 | a0008c0009t0007g0120 a0008c0009t0007g0121 a0008c0009t0007g0123 others(4): Show |
9 | HG02109.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.984+48A>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70183907 | |||||||
chr16:70183950 | C | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(181): Show |
309 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(306): Show |
intron_variant | MODIFIER | c.984+91C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70183950 | |||||||
chr16:70183952 | C | T | 30 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0109 others(27): Show |
38 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.984+93C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70183952 | |||||||
chr16:70183953 | G | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(111): Show |
203 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.984+94G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70183953 | |||||||
chr16:70183996 | G | A | 1 | a0017c0025t0014g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.984+137G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70183996 | |||||||
chr16:70184185 | A | G | 68 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(65): Show |
104 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.985-309A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70184185 | |||||||
chr16:70184213 | T | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(180): Show |
308 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.985-281T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70184213 | |||||||
chr16:70184272 | C | T | 1 | a0011c0026t0009g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.985-222C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70184272 | |||||||
chr16:70184284 | G | A | 69 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(66): Show |
105 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.985-210G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70184284 | |||||||
chr16:70184301 | C | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(166): Show |
283 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.985-193C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70184301 | |||||||
chr16:70184423 | G | A | 68 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(65): Show |
104 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.985-71G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70184423 | |||||||
chr16:70184450 | G | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
197 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.985-44G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70184450 | |||||||
chr16:70184450 | G | T | 3 | a0001c0001t0008g0012 a0001c0001t0013g0012 a0001c0001t0013g0178 |
6 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.985-44G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70184450 | |||||||
chr16:70184462 | C | A | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.985-32C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 9/12 | chr16 | 70184462 | |||||||
chr16:70184668 | A | G | 1 | a0017c0025t0014g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1114+45A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/12 | chr16 | 70184668 | |||||||
chr16:70184765 | C | G | 1 | a0001c0001t0003g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1115-131C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/12 | chr16 | 70184765 | |||||||
chr16:70184781 | A | G | 1 | a0017c0025t0014g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1115-115A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/12 | chr16 | 70184781 | |||||||
chr16:70184789 | A | T | 1 | a0002c0011t0017g0047 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1115-107A>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/12 | chr16 | 70184789 | |||||||
chr16:70184792 | T | A | 1 | a0001c0001t0003g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1115-104T>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/12 | chr16 | 70184792 | |||||||
chr16:70184816 | C | T | 68 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(65): Show |
102 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1115-80C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/12 | chr16 | 70184816 | |||||||
chr16:70184888 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG01358.hp1 HG01496.hp2 |
splice_region_variant&intron_variant | LOW | c.1115-8C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 10/12 | chr16 | 70184888 | |||||||
chr16:70185042 | G | A | 68 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(65): Show |
104 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1211+50G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185042 | |||||||
chr16:70185042 | G | C | 1 | a0026c0017t0002g0052 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1211+50G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185042 | |||||||
chr16:70185052 | G | GC | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(175): Show |
301 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(298): Show |
intron_variant | MODIFIER | c.1211+66dupC | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 70185052 | ||||||
chr16:70185064 | G | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(110): Show |
202 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1211+72G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185064 | |||||||
chr16:70185088 | G | A | 1 | a0001c0001t0003g0139 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1211+96G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185088 | |||||||
chr16:70185142 | G | A | 1 | a0019c0028t0006g0103 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1211+150G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185142 | |||||||
chr16:70185150 | C | T | 1 | a0001c0001t0013g0178 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1211+158C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185150 | |||||||
chr16:70185171 | G | T | 1 | a0004c0004t0005g0109 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1211+179G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185171 | |||||||
chr16:70185172 | C | A | 1 | a0004c0004t0005g0109 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1211+180C>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185172 | |||||||
chr16:70185177 | C | T | 7 | a0001c0001t0003g0009 a0001c0001t0003g0036 a0001c0001t0003g0042 others(4): Show |
14 | HG00639.hp1 HG01106.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1211+185C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185177 | |||||||
chr16:70185178 | G | A | 5 | a0001c0001t0003g0139 a0001c0001t0018g0182 a0007c0007t0004g0126 others(2): Show |
5 | HG02083.hp2 HG02132.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1211+186G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185178 | |||||||
chr16:70185190 | A | AC | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(179): Show |
307 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(304): Show |
intron_variant | MODIFIER | c.1211+199dupC | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 70185190 | ||||||
chr16:70185251 | G | GC | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(180): Show |
308 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.1211+259_1211+260i others(3): Show |
CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185251 | |||||||
chr16:70185264 | C | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(180): Show |
308 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.1211+272C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185264 | |||||||
chr16:70185292 | G | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(180): Show |
308 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.1211+300G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185292 | |||||||
chr16:70185426 | C | T | 1 | a0009c0010t0005g0020 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1211+434C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185426 | |||||||
chr16:70185456 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0164 others(1): Show |
7 | HG01358.hp1 HG01496.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1212-429C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185456 | |||||||
chr16:70185458 | A | G | 45 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(42): Show |
75 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1212-427A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185458 | |||||||
chr16:70185482 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1212-403G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185482 | |||||||
chr16:70185486 | G | A | 2 | a0008c0009t0007g0120 a0008c0009t0007g0124 |
2 | HG02109.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1212-399G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185486 | |||||||
chr16:70185487 | G | T | 67 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(64): Show |
103 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1212-398G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185487 | |||||||
chr16:70185542 | C | T | 39 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(36): Show |
67 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1212-343C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185542 | |||||||
chr16:70185561 | C | G | 69 | a0001c0001t0003g0084 a0002c0002t0002g0002 a0002c0002t0002g0010 others(66): Show |
103 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.1212-324C>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185561 | |||||||
chr16:70185575 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1212-310G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185575 | |||||||
chr16:70185601 | G | A | 12 | a0001c0001t0003g0084 a0004c0004t0005g0016 a0004c0004t0005g0106 others(9): Show |
14 | HG02055.hp1 HG02258.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1212-284G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185601 | |||||||
chr16:70185629 | G | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(111): Show |
203 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1212-256G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185629 | |||||||
chr16:70185756 | G | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(141): Show |
241 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1212-129G>A | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185756 | |||||||
chr16:70185773 | G | T | 1 | a0009c0010t0005g0020 | 3 | HG02723.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1212-112G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185773 | |||||||
chr16:70185791 | C | T | 30 | a0004c0004t0005g0016 a0004c0004t0005g0106 a0004c0004t0005g0109 others(27): Show |
38 | HG01433.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.1212-94C>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185791 | |||||||
chr16:70185874 | A | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(180): Show |
308 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.1212-11A>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 11/12 | chr16 | 70185874 | |||||||
chr16:70185991 | G | C | 39 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(36): Show |
67 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1303+15G>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 12/12 | chr16 | 70185991 | |||||||
chr16:70186011 | T | C | 71 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(68): Show |
107 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1303+35T>C | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 12/12 | chr16 | 70186011 | |||||||
chr16:70186256 | G | T | 70 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0024 others(67): Show |
106 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1304-227G>T | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 12/12 | chr16 | 70186256 | |||||||
chr16:70186417 | A | G | 73 | a0001c0001t0003g0139 a0002c0002t0002g0002 a0002c0002t0002g0010 others(70): Show |
109 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1304-66A>G | CLEC18C | ENSG00000157335.21 | transcript | ENST00000541793.7 | protein_coding | 12/12 | chr16 | 70186417 |