Item | Value |
---|---|
geneid | 284498 |
ensemblid | ENSG00000215910.8 |
hgncid | 25262 |
symbol | C1orf167 |
name | chromosome 1 open reading frame 167 |
refseq_nuc | NM_001010881.2 |
refseq_prot | NP_001010881.1 |
ensembl_nuc | ENST00000688073.1 |
ensembl_prot | ENSP00000510540.1 |
mane_status | MANE Select |
chr | chr1 |
start | 11762193 |
end | 11789585 |
strand | + |
ver | v1.2 |
region | chr1:11762193-11789585 |
region5000 | chr1:11757193-11794585 |
regionname0 | C1orf167_chr1_11762193_11789585 |
regionname5000 | C1orf167_chr1_11757193_11794585 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1449 | 148 | 14 | 44 | 70 | 6 | 14 | 57 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0002 | 0/1 | 1449 | 42 | 0 | 10 | 15 | 3 | 13 | 11 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0003 | 0/0 | 1449 | 21 | 0 | 4 | 16 | 0 | 1 | 11 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0004 | 1/0 | 1449 | 11 | 9 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0005 | 0/0 | 1449 | 11 | 5 | 4 | 0 | 1 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0006 | 0/0 | 1449 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0007 | 0/0 | 1449 | 9 | 4 | 0 | 1 | 1 | 3 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0008 | 0/0 | 1449 | 8 | 0 | 1 | 7 | 0 | 0 | 5 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0009 | 0/0 | 1449 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0010 | 0/0 | 1449 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0011 | 0/0 | 1098 | 4 | 0 | 2 | 1 | 1 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1093): Show |
chr1 | 11757193 | 11794585 |
a0012 | 0/0 | 1449 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0013 | 0/0 | 1449 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0014 | 0/0 | 443 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(438): Show |
chr1 | 11757193 | 11794585 |
a0015 | 0/0 | 1449 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0016 | 0/0 | 1449 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0017 | 0/0 | 1449 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0018 | 0/0 | 1449 | 3 | 1 | 0 | 1 | 1 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0019 | 0/0 | 1449 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0020 | 0/0 | 1449 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0021 | 0/0 | 1449 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0022 | 0/0 | 1449 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0023 | 0/0 | 1449 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0024 | 0/0 | 1449 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0025 | 0/0 | 1449 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0026 | 0/0 | 1449 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0027 | 0/0 | 1449 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0028 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0029 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0030 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0031 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0032 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0033 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0034 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0035 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0036 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0037 | 0/0 | 525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(520): Show |
chr1 | 11757193 | 11794585 |
a0038 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0039 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0040 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0041 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0042 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0043 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0044 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0045 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0046 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0047 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0048 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0049 | 0/0 | 1449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0050 | 0/0 | 1449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0051 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
a0052 | 0/0 | 1449 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | MELRS others(1444): Show |
chr1 | 11757193 | 11794585 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4347 | 139 | 9 | 42 | 68 | 6 | 14 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0001c0009 | 0/0 | 4347 | 7 | 5 | 2 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0001c0045 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0001c0052 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0002c0002 | 0/1 | 4347 | 42 | 0 | 10 | 15 | 3 | 13 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0003c0003 | 0/0 | 4347 | 20 | 0 | 4 | 15 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0003c0031 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0004c0007 | 1/0 | 4347 | 8 | 7 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0004c0017 | 0/0 | 4347 | 3 | 2 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0005c0004 | 0/0 | 4347 | 11 | 5 | 4 | 0 | 1 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0006c0005 | 0/0 | 4347 | 11 | 11 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0007c0010 | 0/0 | 4347 | 7 | 2 | 0 | 1 | 1 | 3 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0007c0050 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0007c0057 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0008c0006 | 0/0 | 4347 | 8 | 0 | 1 | 7 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0009c0008 | 0/0 | 4347 | 8 | 8 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0010c0011 | 0/0 | 4347 | 5 | 5 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0010c0037 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0011c0020 | 0/0 | 4347 | 3 | 0 | 2 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0011c0064 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0012c0013 | 0/0 | 4347 | 4 | 3 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0013c0014 | 0/0 | 4347 | 4 | 4 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0014c0015 | 0/0 | 4345 | 4 | 4 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4340): Show |
chr1 | 11757193 | 11794585 | ||
a0015c0012 | 0/0 | 4347 | 4 | 4 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0016c0018 | 0/0 | 4347 | 3 | 3 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0017c0021 | 0/0 | 4347 | 3 | 3 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0018c0019 | 0/0 | 4347 | 3 | 1 | 0 | 1 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0019c0026 | 0/0 | 4347 | 2 | 2 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0019c0061 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0020c0024 | 0/0 | 4347 | 2 | 2 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0020c0035 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0021c0016 | 0/0 | 4347 | 3 | 0 | 0 | 2 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0022c0028 | 0/0 | 4347 | 2 | 0 | 0 | 2 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0023c0025 | 0/0 | 4347 | 2 | 0 | 1 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0024c0046 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0024c0059 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0025c0023 | 0/0 | 4347 | 2 | 0 | 0 | 2 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0026c0027 | 0/0 | 4347 | 2 | 0 | 0 | 2 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0027c0022 | 0/0 | 4347 | 2 | 0 | 0 | 2 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0028c0048 | 0/0 | 4347 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0029c0033 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0030c0053 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0031c0054 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0032c0047 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0033c0056 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0034c0030 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0035c0062 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0036c0032 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0037c0060 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0038c0034 | 0/0 | 4347 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0039c0043 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0040c0063 | 0/0 | 4347 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0041c0058 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0042c0040 | 0/0 | 4347 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0043c0041 | 0/0 | 4347 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0044c0055 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0045c0029 | 0/0 | 4347 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0046c0044 | 0/0 | 4347 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0047c0051 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0048c0042 | 0/0 | 4347 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0049c0038 | 0/0 | 4347 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0050c0036 | 0/0 | 4347 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0051c0039 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 | ||
a0052c0049 | 0/0 | 4347 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | ATGGA others(4342): Show |
chr1 | 11757193 | 11794585 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4672 | 139 | 9 | 42 | 68 | 6 | 14 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0001c0009t0001 | 0/0 | 4672 | 7 | 5 | 2 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0001c0045t0001 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0001c0052t0001 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0002c0002t0001 | 0/1 | 4672 | 42 | 0 | 10 | 15 | 3 | 13 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0003c0003t0001 | 0/0 | 4672 | 20 | 0 | 4 | 15 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0003c0031t0001 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0004c0007t0001 | 1/0 | 4672 | 8 | 7 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0004c0017t0001 | 0/0 | 4672 | 3 | 2 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0005c0004t0001 | 0/0 | 4672 | 11 | 5 | 4 | 0 | 1 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0006c0005t0001 | 0/0 | 4672 | 8 | 8 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0006c0005t0002 | 0/0 | 4672 | 3 | 3 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0007c0010t0001 | 0/0 | 4672 | 7 | 2 | 0 | 1 | 1 | 3 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0007c0050t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0007c0057t0003 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0008c0006t0001 | 0/0 | 4672 | 8 | 0 | 1 | 7 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0009c0008t0001 | 0/0 | 4672 | 8 | 8 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0010c0011t0001 | 0/0 | 4672 | 4 | 4 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0010c0011t0005 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0010c0037t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0011c0020t0001 | 0/0 | 4672 | 3 | 0 | 2 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0011c0064t0001 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0012c0013t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0012c0013t0002 | 0/0 | 4672 | 2 | 1 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0012c0013t0004 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0013c0014t0001 | 0/0 | 4672 | 4 | 4 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0014c0015t0001 | 0/0 | 4670 | 4 | 4 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4665): Show |
chr1 | 11757193 | 11794585 |
a0015c0012t0001 | 0/0 | 4672 | 4 | 4 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0016c0018t0001 | 0/0 | 4672 | 3 | 3 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0017c0021t0001 | 0/0 | 4672 | 3 | 3 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0018c0019t0001 | 0/0 | 4672 | 3 | 1 | 0 | 1 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0019c0026t0001 | 0/0 | 4672 | 2 | 2 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0019c0061t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0020c0024t0001 | 0/0 | 4672 | 2 | 2 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0020c0035t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0021c0016t0001 | 0/0 | 4672 | 3 | 0 | 0 | 2 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0022c0028t0001 | 0/0 | 4672 | 2 | 0 | 0 | 2 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0023c0025t0001 | 0/0 | 4672 | 2 | 0 | 1 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0024c0046t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0024c0059t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0025c0023t0001 | 0/0 | 4672 | 2 | 0 | 0 | 2 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0026c0027t0001 | 0/0 | 4672 | 2 | 0 | 0 | 2 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0027c0022t0001 | 0/0 | 4672 | 2 | 0 | 0 | 2 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0028c0048t0001 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0029c0033t0001 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0030c0053t0001 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0031c0054t0001 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0032c0047t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0033c0056t0001 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0034c0030t0001 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0035c0062t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0036c0032t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0037c0060t0003 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0038c0034t0001 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0039c0043t0002 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0040c0063t0001 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0041c0058t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0042c0040t0001 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0043c0041t0001 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0044c0055t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0045c0029t0001 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0046c0044t0001 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0047c0051t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0048c0042t0001 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0049c0038t0001 | 0/0 | 4672 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0050c0036t0001 | 0/0 | 4672 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0051c0039t0001 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
a0052c0049t0001 | 0/0 | 4672 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | GACGT others(4667): Show |
chr1 | 11757193 | 11794585 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0009t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0009t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0009t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0009t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0009t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0045t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0001c0052t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0003c0031t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0004c0007t0001g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0004c0007t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0004c0007t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0004c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0004c0007t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0004c0007t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0004c0007t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0004c0007t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0004c0017t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0004c0017t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0004c0017t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0005c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0005c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0005c0004t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0005c0004t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0005c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0005c0004t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0005c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0005c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0005c0004t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0005c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0005c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0006c0005t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0006c0005t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0006c0005t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0006c0005t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0006c0005t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0006c0005t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0006c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0006c0005t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0006c0005t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0006c0005t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0007c0010t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0007c0010t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0007c0010t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0007c0010t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0007c0010t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0007c0010t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0007c0010t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0007c0050t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0007c0057t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0008c0006t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0008c0006t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0008c0006t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0008c0006t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0008c0006t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0008c0006t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0008c0006t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0008c0006t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0009c0008t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0009c0008t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0009c0008t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0009c0008t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0009c0008t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0009c0008t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0009c0008t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0009c0008t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0010c0011t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0010c0011t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0010c0011t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0010c0011t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0010c0011t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0010c0037t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0011c0020t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0011c0020t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0011c0020t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0011c0064t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0012c0013t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0012c0013t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0012c0013t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0012c0013t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0013c0014t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0013c0014t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0013c0014t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0013c0014t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0014c0015t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0014c0015t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0014c0015t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0014c0015t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0015c0012t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0015c0012t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0015c0012t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0015c0012t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0016c0018t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0016c0018t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0016c0018t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0017c0021t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0017c0021t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0017c0021t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0018c0019t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0018c0019t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0018c0019t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0019c0026t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0019c0026t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0019c0061t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0020c0024t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0020c0024t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0020c0035t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0021c0016t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0021c0016t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0021c0016t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0022c0028t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0022c0028t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0023c0025t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0023c0025t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0024c0046t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0024c0059t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0025c0023t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0025c0023t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0026c0027t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0026c0027t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0027c0022t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0027c0022t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0028c0048t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0029c0033t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0030c0053t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0031c0054t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0032c0047t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0033c0056t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0034c0030t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0035c0062t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0036c0032t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0037c0060t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0038c0034t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0039c0043t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0040c0063t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0041c0058t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0042c0040t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0043c0041t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0044c0055t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0045c0029t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0046c0044t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0047c0051t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0048c0042t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0049c0038t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0050c0036t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0051c0039t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
a0052c0049t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0007 | c0010 | t0001 | g0050 | EUR | GBR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0175 | EUR | GBR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | GBR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00140 | hp2 | a0005 | c0004 | t0001 | g0293 | EUR | GBR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | FIN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00323 | hp2 | a0028 | c0048 | t0001 | g0287 | EUR | FIN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00438 | hp1 | a0029 | c0033 | t0001 | g0291 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00544 | hp1 | a0030 | c0053 | t0001 | g0304 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00597 | hp1 | a0003 | c0003 | t0001 | g0277 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00609 | hp1 | a0003 | c0003 | t0001 | g0166 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00609 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00621 | hp1 | a0031 | c0054 | t0001 | g0228 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0279 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00642 | hp1 | a0005 | c0004 | t0001 | g0144 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00642 | hp2 | a0003 | c0003 | t0001 | g0307 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0179 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01069 | hp1 | a0011 | c0020 | t0001 | g0082 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01071 | hp1 | a0011 | c0020 | t0001 | g0081 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01074 | hp1 | a0005 | c0004 | t0001 | g0256 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0202 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01106 | hp2 | a0003 | c0003 | t0001 | g0306 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01109 | hp2 | a0012 | c0013 | t0002 | g0147 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01167 | hp2 | a0001 | c0009 | t0001 | g0128 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01192 | hp1 | a0001 | c0009 | t0001 | g0006 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01243 | hp1 | a0004 | c0017 | t0001 | g0046 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0283 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01358 | hp1 | a0005 | c0004 | t0001 | g0185 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01361 | hp2 | a0008 | c0006 | t0001 | g0055 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0323 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01884 | hp1 | a0016 | c0018 | t0001 | g0155 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01884 | hp2 | a0032 | c0047 | t0001 | g0063 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01891 | hp1 | a0004 | c0007 | t0001 | g0150 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01891 | hp2 | a0012 | c0013 | t0004 | g0117 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01934 | hp1 | a0003 | c0003 | t0001 | g0284 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02004 | hp1 | a0005 | c0004 | t0001 | g0098 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02015 | hp1 | a0033 | c0056 | t0001 | g0085 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02040 | hp2 | a0022 | c0028 | t0001 | g0271 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02055 | hp1 | a0007 | c0010 | t0001 | g0035 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02055 | hp2 | a0013 | c0014 | t0001 | g0047 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02056 | hp1 | a0008 | c0006 | t0001 | g0186 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0203 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02074 | hp1 | a0022 | c0028 | t0001 | g0248 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02074 | hp2 | a0034 | c0030 | t0001 | g0076 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02080 | hp2 | a0003 | c0003 | t0001 | g0297 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02132 | hp2 | a0007 | c0010 | t0001 | g0049 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02145 | hp1 | a0013 | c0014 | t0001 | g0022 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02145 | hp2 | a0016 | c0018 | t0001 | g0028 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02165 | hp1 | a0003 | c0003 | t0001 | g0298 | EAS | CDX | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CDX | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02257 | hp1 | a0009 | c0008 | t0001 | g0114 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02257 | hp2 | a0007 | c0010 | t0001 | g0039 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02258 | hp1 | a0014 | c0015 | t0001 | g0017 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02280 | hp1 | a0014 | c0015 | t0001 | g0133 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02280 | hp2 | a0009 | c0008 | t0001 | g0043 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02293 | hp1 | a0023 | c0025 | t0001 | g0196 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02451 | hp1 | a0001 | c0009 | t0001 | g0126 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02451 | hp2 | a0001 | c0009 | t0001 | g0038 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02572 | hp1 | a0018 | c0019 | t0001 | g0153 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02572 | hp2 | a0009 | c0008 | t0001 | g0122 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02602 | hp1 | a0007 | c0010 | t0001 | g0172 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02615 | hp1 | a0036 | c0032 | t0001 | g0095 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02615 | hp2 | a0037 | c0060 | t0003 | g0113 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02622 | hp1 | a0009 | c0008 | t0001 | g0042 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02622 | hp2 | a0015 | c0012 | t0001 | g0018 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02630 | hp1 | a0010 | c0011 | t0001 | g0034 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02630 | hp2 | a0019 | c0026 | t0001 | g0068 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02647 | hp1 | a0006 | c0005 | t0002 | g0020 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02647 | hp2 | a0015 | c0012 | t0001 | g0094 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02698 | hp1 | a0038 | c0034 | t0001 | g0322 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02717 | hp1 | a0012 | c0013 | t0002 | g0030 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02717 | hp2 | a0004 | c0007 | t0001 | g0112 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02723 | hp2 | a0039 | c0043 | t0002 | g0021 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02735 | hp1 | a0040 | c0063 | t0001 | g0004 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02738 | hp2 | a0005 | c0004 | t0001 | g0064 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02809 | hp1 | a0004 | c0017 | t0001 | g0251 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02809 | hp2 | a0024 | c0046 | t0001 | g0009 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02886 | hp1 | a0004 | c0007 | t0001 | g0252 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02886 | hp2 | a0006 | c0005 | t0001 | g0026 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02895 | hp1 | a0010 | c0037 | t0001 | g0036 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02895 | hp2 | a0015 | c0012 | t0001 | g0328 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02896 | hp1 | a0001 | c0009 | t0001 | g0053 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02896 | hp2 | a0004 | c0007 | t0001 | g0100 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02897 | hp1 | a0015 | c0012 | t0001 | g0327 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02897 | hp2 | a0001 | c0009 | t0001 | g0006 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02922 | hp1 | a0005 | c0004 | t0001 | g0145 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02922 | hp2 | a0005 | c0004 | t0001 | g0257 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02965 | hp1 | a0020 | c0024 | t0001 | g0151 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02965 | hp2 | a0006 | c0005 | t0001 | g0012 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02970 | hp1 | a0004 | c0007 | t0001 | g0062 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02970 | hp2 | a0006 | c0005 | t0001 | g0032 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02976 | hp1 | a0041 | c0058 | t0001 | g0167 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02976 | hp2 | a0006 | c0005 | t0001 | g0148 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03017 | hp1 | a0042 | c0040 | t0001 | g0317 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03017 | hp2 | a0043 | c0041 | t0001 | g0288 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03041 | hp1 | a0010 | c0011 | t0001 | g0045 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03098 | hp1 | a0017 | c0021 | t0001 | g0052 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03098 | hp2 | a0044 | c0055 | t0001 | g0024 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03130 | hp1 | a0009 | c0008 | t0001 | g0048 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03130 | hp2 | a0020 | c0024 | t0001 | g0132 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03139 | hp2 | a0024 | c0059 | t0001 | g0009 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03195 | hp1 | a0006 | c0005 | t0001 | g0025 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03195 | hp2 | a0009 | c0008 | t0001 | g0124 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03225 | hp1 | a0020 | c0035 | t0001 | g0040 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03225 | hp2 | a0013 | c0014 | t0001 | g0121 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03239 | hp1 | a0023 | c0025 | t0001 | g0250 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03239 | hp2 | a0045 | c0029 | t0001 | g0218 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03453 | hp1 | a0006 | c0005 | t0001 | g0012 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03453 | hp2 | a0007 | c0057 | t0003 | g0019 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03486 | hp1 | a0004 | c0017 | t0001 | g0044 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03486 | hp2 | a0010 | c0011 | t0001 | g0134 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03491 | hp1 | a0021 | c0016 | t0001 | g0276 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03492 | hp2 | a0046 | c0044 | t0001 | g0219 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03516 | hp1 | a0014 | c0015 | t0001 | g0116 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03516 | hp2 | a0005 | c0004 | t0001 | g0254 | AFR | ESN | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03540 | hp1 | a0006 | c0005 | t0002 | g0023 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03540 | hp2 | a0047 | c0051 | t0001 | g0029 | AFR | GWD | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03579 | hp1 | a0014 | c0015 | t0001 | g0115 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03669 | hp1 | a0048 | c0042 | t0001 | g0299 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0295 | SAS | STU | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0097 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03831 | hp1 | a0003 | c0003 | t0001 | g0258 | SAS | BEB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03831 | hp2 | a0007 | c0010 | t0001 | g0173 | SAS | BEB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | BEB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0253 | SAS | BEB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03927 | hp2 | a0007 | c0010 | t0001 | g0199 | SAS | BEB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03942 | hp1 | a0049 | c0038 | t0001 | g0077 | SAS | BEB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0174 | SAS | STU | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | STU | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18522 | hp1 | a0017 | c0021 | t0001 | g0146 | AFR | YRI | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18522 | hp2 | a0006 | c0005 | t0001 | g0125 | AFR | YRI | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18747 | hp1 | a0008 | c0006 | t0001 | g0205 | EAS | CHB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | CHB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18906 | hp1 | a0016 | c0018 | t0001 | g0051 | AFR | YRI | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18906 | hp2 | a0010 | c0011 | t0001 | g0135 | AFR | YRI | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18944 | hp2 | a0003 | c0031 | t0001 | g0229 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18951 | hp2 | a0011 | c0064 | t0001 | g0170 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18954 | hp1 | a0051 | c0039 | t0001 | g0201 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18959 | hp2 | a0025 | c0023 | t0001 | g0261 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18961 | hp1 | a0003 | c0003 | t0001 | g0263 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18961 | hp2 | a0001 | c0045 | t0001 | g0249 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18967 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18969 | hp1 | a0026 | c0027 | t0001 | g0004 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18970 | hp2 | a0052 | c0049 | t0001 | g0230 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18971 | hp2 | a0027 | c0022 | t0001 | g0169 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18972 | hp2 | a0008 | c0006 | t0001 | g0206 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18981 | hp2 | a0003 | c0003 | t0001 | g0075 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18984 | hp1 | a0018 | c0019 | t0001 | g0247 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18984 | hp2 | a0003 | c0003 | t0001 | g0207 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18986 | hp2 | a0021 | c0016 | t0001 | g0289 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18993 | hp2 | a0008 | c0006 | t0001 | g0316 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19000 | hp2 | a0003 | c0003 | t0001 | g0300 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19030 | hp1 | a0004 | c0007 | t0001 | g0041 | AFR | LWK | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19030 | hp2 | a0007 | c0050 | t0001 | g0119 | AFR | LWK | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19043 | hp1 | a0019 | c0026 | t0001 | g0096 | AFR | LWK | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19043 | hp2 | a0009 | c0008 | t0001 | g0136 | AFR | LWK | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19055 | hp1 | a0027 | c0022 | t0001 | g0198 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19057 | hp1 | a0008 | c0006 | t0001 | g0078 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19064 | hp1 | a0026 | c0027 | t0001 | g0211 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19067 | hp2 | a0003 | c0003 | t0001 | g0208 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19074 | hp2 | a0008 | c0006 | t0001 | g0209 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19079 | hp1 | a0003 | c0003 | t0001 | g0105 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19081 | hp1 | a0008 | c0006 | t0001 | g0106 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19081 | hp2 | a0003 | c0003 | t0001 | g0111 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19084 | hp1 | a0025 | c0023 | t0001 | g0262 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19085 | hp1 | a0003 | c0003 | t0001 | g0296 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19088 | hp1 | a0001 | c0052 | t0001 | g0086 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0204 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19089 | hp2 | a0021 | c0016 | t0001 | g0197 | EAS | JPT | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19240 | hp1 | a0010 | c0011 | t0005 | g0033 | AFR | YRI | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA19240 | hp2 | a0006 | c0005 | t0002 | g0061 | AFR | YRI | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA20129 | hp1 | a0019 | c0061 | t0001 | g0319 | AFR | ASW | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ASW | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0180 | EUR | TSI | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA20752 | hp2 | a0011 | c0020 | t0001 | g0056 | EUR | TSI | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA20805 | hp1 | a0018 | c0019 | t0001 | g0093 | EUR | TSI | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0070 | EUR | TSI | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0294 | SAS | GIH | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | GIH | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02109 | hp1 | a0017 | c0021 | t0001 | g0154 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02109 | hp2 | a0035 | c0062 | t0001 | g0260 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02486 | hp1 | a0005 | c0004 | t0001 | g0071 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02559 | hp1 | a0013 | c0014 | t0001 | g0118 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG02559 | hp2 | a0006 | c0005 | t0001 | g0101 | AFR | ACB | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03471 | hp1 | a0012 | c0013 | t0001 | g0120 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG03471 | hp2 | a0009 | c0008 | t0001 | g0123 | AFR | MSL | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG06807 | hp1 | a0050 | c0036 | t0001 | g0149 | AFR | USA | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
HG06807 | hp2 | a0004 | c0007 | t0001 | g0137 | AFR | USA | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | USA | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA20300 | hp2 | a0005 | c0004 | t0001 | g0255 | AFR | USA | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA21309 | hp1 | a0001 | c0009 | t0001 | g0102 | AFR | LWK | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0139 | REF | REF | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
homoSapiens | grch38p0 | a0004 | c0007 | t0001 | g0037 | REF | REF | C1orf167_chr1_11757193_11794585 | C1orf167 | chr1 | 11757193 | 11794585 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11762305 | C | T | 3 | a0006 a0012 a0039 |
6 | HG01109.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
splice_region_variant | LOW | c.-71C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/21 | chr1 | 11762305 | |||||||
chr1:11765889 | G | A | 1 | a0045 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.103G>A | p.Gly35Ser | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 286/4672 | 103/4350 | 35/1449 | chr1 | 11765889 | |||
chr1:11765976 | C | G | 1 | a0040 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.190C>G | p.Leu64Val | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 373/4672 | 190/4350 | 64/1449 | chr1 | 11765976 | |||
chr1:11766028 | G | A | 4 | a0003 a0008 a0025 others(1): Show |
32 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(29): Show |
missense_variant | MODERATE | c.242G>A | p.Arg81His | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 425/4672 | 242/4350 | 81/1449 | chr1 | 11766028 | |||
chr1:11766129 | G | T | 2 | a0021 a0027 |
5 | HG03491.hp1 NA18971.hp2 NA18986.hp2 others(2): Show |
missense_variant | MODERATE | c.343G>T | p.Ala115Ser | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 526/4672 | 343/4350 | 115/1449 | chr1 | 11766129 | |||
chr1:11766237 | G | T | 1 | a0035 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.451G>T | p.Gly151Cys | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 634/4672 | 451/4350 | 151/1449 | chr1 | 11766237 | |||
chr1:11766294 | G | A | 3 | a0021 a0027 a0036 |
6 | HG02615.hp1 HG03491.hp1 NA18971.hp2 others(3): Show |
missense_variant | MODERATE | c.508G>A | p.Gly170Arg | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 691/4672 | 508/4350 | 170/1449 | chr1 | 11766294 | |||
chr1:11766364 | A | G | 2 | a0013 a0014 |
8 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
missense_variant | MODERATE | c.578A>G | p.His193Arg | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 761/4672 | 578/4350 | 193/1449 | chr1 | 11766364 | |||
chr1:11766493 | C | T | 1 | a0025 | 2 | NA18959.hp2 NA19084.hp1 |
missense_variant | MODERATE | c.707C>T | p.Ala236Val | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 890/4672 | 707/4350 | 236/1449 | chr1 | 11766493 | |||
chr1:11766544 | G | A | 1 | a0038 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.758G>A | p.Arg253Gln | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 941/4672 | 758/4350 | 253/1449 | chr1 | 11766544 | |||
chr1:11766570 | C | G | 1 | a0037 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.784C>G | p.Pro262Ala | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 967/4672 | 784/4350 | 262/1449 | chr1 | 11766570 | |||
chr1:11766573 | C | T | 26 | a0001 a0006 a0007 others(23): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
missense_variant | MODERATE | c.787C>T | p.Pro263Ser | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 970/4672 | 787/4350 | 263/1449 | chr1 | 11766573 | |||
chr1:11766606 | G | A | 1 | a0046 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.820G>A | p.Gly274Ser | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 1003/4672 | 820/4350 | 274/1449 | chr1 | 11766606 | |||
chr1:11766804 | A | C | 2 | a0014 a0037 |
5 | HG02258.hp1 HG02280.hp1 HG02615.hp2 others(2): Show |
missense_variant | MODERATE | c.1018A>C | p.Asn340His | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 1201/4672 | 1018/4350 | 340/1449 | chr1 | 11766804 | |||
chr1:11766922 | G | T | 1 | a0029 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1136G>T | p.Ser379Ile | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 1319/4672 | 1136/4350 | 379/1449 | chr1 | 11766922 | |||
chr1:11766933 | G | A | 1 | a0016 | 3 | HG01884.hp1 HG02145.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.1147G>A | p.Asp383Asn | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 1330/4672 | 1147/4350 | 383/1449 | chr1 | 11766933 | |||
chr1:11767014 | C | T | 2 | a0013 a0014 |
8 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
missense_variant | MODERATE | c.1228C>T | p.Arg410Trp | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 1411/4672 | 1228/4350 | 410/1449 | chr1 | 11767014 | |||
chr1:11767056 | GAC | G | 1 | a0014 | 4 | HG02258.hp1 HG02280.hp1 HG03516.hp1 others(1): Show |
frameshift_variant | HIGH | c.1274_1275delCA | p.Thr425fs | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 1457/4672 | 1274/4350 | 425/1449 | INFO_REALIGN_3_PRIME | chr1 | 11767056 | ||
chr1:11767252 | C | T | 1 | a0037 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.1331C>T | p.Ser444Phe | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 4/21 | 1514/4672 | 1331/4350 | 444/1449 | chr1 | 11767252 | |||
chr1:11768181 | G | A | 24 | a0001 a0006 a0007 others(21): Show |
204 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(201): Show |
missense_variant | MODERATE | c.1448G>A | p.Arg483Gln | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/21 | 1631/4672 | 1448/4350 | 483/1449 | chr1 | 11768181 | |||
chr1:11768249 | G | A | 1 | a0029 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1516G>A | p.Val506Ile | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/21 | 1699/4672 | 1516/4350 | 506/1449 | chr1 | 11768249 | |||
chr1:11768262 | G | A | 24 | a0001 a0006 a0007 others(21): Show |
204 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(201): Show |
missense_variant | MODERATE | c.1529G>A | p.Arg510Gln | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/21 | 1712/4672 | 1529/4350 | 510/1449 | chr1 | 11768262 | |||
chr1:11769006 | C | T | 1 | a0037 | 1 | HG02615.hp2 | stop_gained | HIGH | c.1576C>T | p.Gln526* | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/21 | 1759/4672 | 1576/4350 | 526/1449 | chr1 | 11769006 | |||
chr1:11771538 | G | A | 5 | a0005 a0021 a0024 others(2): Show |
19 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(16): Show |
missense_variant | MODERATE | c.1712G>A | p.Arg571Lys | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 7/21 | 1895/4672 | 1712/4350 | 571/1449 | chr1 | 11771538 | |||
chr1:11771558 | C | T | 28 | a0001 a0003 a0007 others(25): Show |
234 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(231): Show |
missense_variant | MODERATE | c.1732C>T | p.Arg578Trp | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 7/21 | 1915/4672 | 1732/4350 | 578/1449 | chr1 | 11771558 | |||
chr1:11772139 | G | A | 1 | a0049 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.1868G>A | p.Arg623Gln | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/21 | 2051/4672 | 1868/4350 | 623/1449 | chr1 | 11772139 | |||
chr1:11772232 | C | A | 4 | a0002 a0018 a0042 others(1): Show |
46 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(43): Show |
missense_variant | MODERATE | c.1961C>A | p.Pro654His | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/21 | 2144/4672 | 1961/4350 | 654/1449 | chr1 | 11772232 | |||
chr1:11775442 | G | A | 1 | a0034 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.1996G>A | p.Gly666Arg | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/21 | 2179/4672 | 1996/4350 | 666/1449 | chr1 | 11775442 | |||
chr1:11775475 | C | G | 1 | a0033 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.2029C>G | p.Arg677Gly | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/21 | 2212/4672 | 2029/4350 | 677/1449 | chr1 | 11775475 | |||
chr1:11775476 | G | A | 1 | a0043 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.2030G>A | p.Arg677Gln | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/21 | 2213/4672 | 2030/4350 | 677/1449 | chr1 | 11775476 | |||
chr1:11775499 | C | T | 10 | a0003 a0007 a0012 others(7): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
missense_variant | MODERATE | c.2053C>T | p.Arg685Cys | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/21 | 2236/4672 | 2053/4350 | 685/1449 | chr1 | 11775499 | |||
chr1:11775556 | C | T | 1 | a0026 | 2 | NA18969.hp1 NA19064.hp1 |
missense_variant | MODERATE | c.2110C>T | p.Arg704Trp | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/21 | 2293/4672 | 2110/4350 | 704/1449 | chr1 | 11775556 | |||
chr1:11776496 | G | T | 2 | a0015 a0044 |
5 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
missense_variant | MODERATE | c.2197G>T | p.Ala733Ser | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/21 | 2380/4672 | 2197/4350 | 733/1449 | chr1 | 11776496 | |||
chr1:11776571 | T | C | 30 | a0001 a0003 a0007 others(27): Show |
237 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(234): Show |
missense_variant | MODERATE | c.2272T>C | p.Trp758Arg | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/21 | 2455/4672 | 2272/4350 | 758/1449 | chr1 | 11776571 | |||
chr1:11776625 | C | T | 20 | a0001 a0008 a0010 others(17): Show |
191 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(188): Show |
missense_variant | MODERATE | c.2326C>T | p.Arg776Cys | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/21 | 2509/4672 | 2326/4350 | 776/1449 | chr1 | 11776625 | |||
chr1:11778719 | T | G | 1 | a0051 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.2399T>G | p.Leu800Trp | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 11/21 | 2582/4672 | 2399/4350 | 800/1449 | chr1 | 11778719 | |||
chr1:11778784 | A | G | 10 | a0003 a0007 a0012 others(7): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
missense_variant | MODERATE | c.2464A>G | p.Ser822Gly | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 11/21 | 2647/4672 | 2464/4350 | 822/1449 | chr1 | 11778784 | |||
chr1:11778791 | G | T | 20 | a0001 a0008 a0010 others(17): Show |
191 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(188): Show |
missense_variant | MODERATE | c.2471G>T | p.Ser824Ile | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 11/21 | 2654/4672 | 2471/4350 | 824/1449 | chr1 | 11778791 | |||
chr1:11778976 | G | T | 2 | a0023 a0049 |
3 | HG02293.hp1 HG03239.hp1 HG03942.hp1 |
missense_variant | MODERATE | c.2547G>T | p.Trp849Cys | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/21 | 2730/4672 | 2547/4350 | 849/1449 | chr1 | 11778976 | |||
chr1:11778977 | G | A | 8 | a0003 a0007 a0022 others(5): Show |
38 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(35): Show |
missense_variant | MODERATE | c.2548G>A | p.Ala850Thr | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/21 | 2731/4672 | 2548/4350 | 850/1449 | chr1 | 11778977 | |||
chr1:11779079 | C | T | 1 | a0031 | 1 | HG00621.hp1 | missense_variant&splice_region_variant | MODERATE | c.2650C>T | p.Arg884Cys | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/21 | 2833/4672 | 2650/4350 | 884/1449 | chr1 | 11779079 | |||
chr1:11779866 | C | T | 16 | a0003 a0007 a0013 others(13): Show |
50 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
missense_variant | MODERATE | c.2716C>T | p.Arg906Trp | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/21 | 2899/4672 | 2716/4350 | 906/1449 | chr1 | 11779866 | |||
chr1:11779909 | G | A | 19 | a0001 a0008 a0010 others(16): Show |
190 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(187): Show |
missense_variant | MODERATE | c.2759G>A | p.Arg920His | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/21 | 2942/4672 | 2759/4350 | 920/1449 | chr1 | 11779909 | |||
chr1:11779914 | C | T | 5 | a0005 a0021 a0024 others(2): Show |
18 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(15): Show |
missense_variant | MODERATE | c.2764C>T | p.Arg922Trp | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/21 | 2947/4672 | 2764/4350 | 922/1449 | chr1 | 11779914 | |||
chr1:11779915 | G | A | 5 | a0002 a0012 a0014 others(2): Show |
53 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(50): Show |
missense_variant | MODERATE | c.2765G>A | p.Arg922Gln | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/21 | 2948/4672 | 2765/4350 | 922/1449 | chr1 | 11779915 | |||
chr1:11779941 | T | C | 38 | a0001 a0002 a0003 others(35): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
missense_variant | MODERATE | c.2791T>C | p.Trp931Arg | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/21 | 2974/4672 | 2791/4350 | 931/1449 | chr1 | 11779941 | |||
chr1:11779986 | T | C | 1 | a0032 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.2836T>C | p.Cys946Arg | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/21 | 3019/4672 | 2836/4350 | 946/1449 | chr1 | 11779986 | |||
chr1:11784232 | C | T | 1 | a0011 | 1 | NA18951.hp2 | stop_gained | HIGH | c.3064C>T | p.Gln1022* | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/21 | 3247/4672 | 3064/4350 | 1022/1449 | chr1 | 11784232 | |||
chr1:11784367 | G | A | 2 | a0009 a0019 |
11 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
missense_variant | MODERATE | c.3199G>A | p.Gly1067Arg | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/21 | 3382/4672 | 3199/4350 | 1067/1449 | chr1 | 11784367 | |||
chr1:11784397 | A | C | 5 | a0005 a0021 a0024 others(2): Show |
18 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(15): Show |
missense_variant | MODERATE | c.3229A>C | p.Lys1077Gln | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/21 | 3412/4672 | 3229/4350 | 1077/1449 | chr1 | 11784397 | |||
chr1:11784463 | C | T | 1 | a0011 | 3 | HG01069.hp1 HG01071.hp1 NA20752.hp2 |
stop_gained | HIGH | c.3295C>T | p.Gln1099* | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/21 | 3478/4672 | 3295/4350 | 1099/1449 | chr1 | 11784463 | |||
chr1:11785165 | T | C | 10 | a0003 a0007 a0022 others(7): Show |
40 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(37): Show |
missense_variant | MODERATE | c.3443T>C | p.Val1148Ala | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/21 | 3626/4672 | 3443/4350 | 1148/1449 | chr1 | 11785165 | |||
chr1:11787392 | G | A | 5 | a0003 a0022 a0025 others(2): Show |
27 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(24): Show |
missense_variant | MODERATE | c.3572G>A | p.Arg1191His | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 17/21 | 3755/4672 | 3572/4350 | 1191/1449 | chr1 | 11787392 | |||
chr1:11787875 | T | C | 1 | a0021 | 3 | HG03491.hp1 NA18986.hp2 NA19089.hp2 |
missense_variant&splice_region_variant | MODERATE | c.3676T>C | p.Cys1226Arg | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 18/21 | 3859/4672 | 3676/4350 | 1226/1449 | chr1 | 11787875 | |||
chr1:11788011 | G | C | 9 | a0003 a0007 a0022 others(6): Show |
39 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(36): Show |
missense_variant | MODERATE | c.3812G>C | p.Cys1271Ser | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 18/21 | 3995/4672 | 3812/4350 | 1271/1449 | chr1 | 11788011 | |||
chr1:11789390 | A | G | 48 | a0001 a0002 a0003 others(45): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
missense_variant | MODERATE | c.4294A>G | p.Arg1432Gly | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 21/21 | 4477/4672 | 4294/4350 | 1432/1449 | chr1 | 11789390 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11764466 | G | A | 2 | a0021c0016 a0027c0022 |
5 | HG03491.hp1 NA18971.hp2 NA18986.hp2 others(2): Show |
synonymous_variant | LOW | c.66G>A | p.Lys22Lys | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/21 | 249/4672 | 66/4350 | 22/1449 | chr1 | 11764466 | |||
chr1:11765960 | C | T | 1 | a0011c0064 | 1 | NA18951.hp2 | synonymous_variant | LOW | c.174C>T | p.Pro58Pro | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 357/4672 | 174/4350 | 58/1449 | chr1 | 11765960 | |||
chr1:11766143 | C | T | 2 | a0021c0016 a0027c0022 |
5 | HG03491.hp1 NA18971.hp2 NA18986.hp2 others(2): Show |
synonymous_variant | LOW | c.357C>T | p.Ala119Ala | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 540/4672 | 357/4350 | 119/1449 | chr1 | 11766143 | |||
chr1:11766302 | G | A | 3 | a0021c0016 a0027c0022 a0029c0033 |
6 | HG00438.hp1 HG03491.hp1 NA18971.hp2 others(3): Show |
synonymous_variant | LOW | c.516G>A | p.Pro172Pro | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 699/4672 | 516/4350 | 172/1449 | chr1 | 11766302 | |||
chr1:11766356 | C | T | 1 | a0019c0061 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.570C>T | p.Leu190Leu | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 753/4672 | 570/4350 | 190/1449 | chr1 | 11766356 | |||
chr1:11766608 | C | T | 1 | a0024c0059 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.822C>T | p.Gly274Gly | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 1005/4672 | 822/4350 | 274/1449 | chr1 | 11766608 | |||
chr1:11766701 | T | G | 1 | a0001c0045 | 1 | NA18961.hp2 | synonymous_variant | LOW | c.915T>G | p.Thr305Thr | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 1098/4672 | 915/4350 | 305/1449 | chr1 | 11766701 | |||
chr1:11766923 | C | T | 1 | a0029c0033 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.1137C>T | p.Ser379Ser | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/21 | 1320/4672 | 1137/4350 | 379/1449 | chr1 | 11766923 | |||
chr1:11767247 | A | G | 60 | a0001c0001 a0001c0009 a0001c0045 others(57): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
synonymous_variant | LOW | c.1326A>G | p.Pro442Pro | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 4/21 | 1509/4672 | 1326/4350 | 442/1449 | chr1 | 11767247 | |||
chr1:11772212 | C | A | 3 | a0007c0050 a0012c0013 a0014c0015 |
9 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
synonymous_variant | LOW | c.1941C>A | p.Ala647Ala | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/21 | 2124/4672 | 1941/4350 | 647/1449 | chr1 | 11772212 | |||
chr1:11772254 | G | C | 24 | a0001c0001 a0001c0009 a0001c0045 others(21): Show |
189 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(186): Show |
synonymous_variant | LOW | c.1983G>C | p.Leu661Leu | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/21 | 2166/4672 | 1983/4350 | 661/1449 | chr1 | 11772254 | |||
chr1:11776555 | C | T | 1 | a0021c0016 | 3 | HG03491.hp1 NA18986.hp2 NA19089.hp2 |
synonymous_variant | LOW | c.2256C>T | p.Ser752Ser | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/21 | 2439/4672 | 2256/4350 | 752/1449 | chr1 | 11776555 | |||
chr1:11776613 | C | A | 13 | a0003c0003 a0003c0031 a0007c0010 others(10): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
synonymous_variant | LOW | c.2314C>A | p.Arg772Arg | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/21 | 2497/4672 | 2314/4350 | 772/1449 | chr1 | 11776613 | |||
chr1:11778705 | G | A | 3 | a0007c0010 a0035c0062 a0037c0060 |
9 | HG00099.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
synonymous_variant | LOW | c.2385G>A | p.Leu795Leu | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 11/21 | 2568/4672 | 2385/4350 | 795/1449 | chr1 | 11778705 | |||
chr1:11778952 | C | T | 13 | a0003c0003 a0003c0031 a0007c0010 others(10): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
synonymous_variant | LOW | c.2523C>T | p.Asp841Asp | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/21 | 2706/4672 | 2523/4350 | 841/1449 | chr1 | 11778952 | |||
chr1:11784273 | C | T | 17 | a0001c0001 a0001c0045 a0001c0052 others(14): Show |
166 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(163): Show |
synonymous_variant | LOW | c.3105C>T | p.Ala1035Ala | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/21 | 3288/4672 | 3105/4350 | 1035/1449 | chr1 | 11784273 | |||
chr1:11784366 | C | T | 1 | a0001c0052 | 1 | NA19088.hp1 | synonymous_variant | LOW | c.3198C>T | p.Cys1066Cys | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/21 | 3381/4672 | 3198/4350 | 1066/1449 | chr1 | 11784366 | |||
chr1:11787393 | C | G | 1 | a0003c0031 | 1 | NA18944.hp2 | synonymous_variant | LOW | c.3573C>G | p.Arg1191Arg | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 17/21 | 3756/4672 | 3573/4350 | 1191/1449 | chr1 | 11787393 | |||
chr1:11787997 | T | C | 3 | a0009c0008 a0019c0026 a0019c0061 |
11 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
synonymous_variant | LOW | c.3798T>C | p.Pro1266Pro | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 18/21 | 3981/4672 | 3798/4350 | 1266/1449 | chr1 | 11787997 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11762209 | C | G | 2 | a0007c0057t0003 a0037c0060t0003 |
2 | HG02615.hp2 HG03453.hp2 |
5_prime_UTR_variant | MODIFIER | c.-167C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/21 | 2192 | chr1 | 11762209 | ||||||
chr1:11762248 | C | T | 1 | a0010c0011t0005 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-128C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/21 | 2153 | chr1 | 11762248 | ||||||
chr1:11789566 | A | C | 1 | a0012c0013t0004 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 21/21 | 120 | chr1 | 11789566 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11762437 | C | T | 2 | a0015c0012t0001g0327 a0015c0012t0001g0328 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-71+132C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11762437 | |||||||
chr1:11762538 | G | T | 9 | a0001c0001t0001g0318 a0001c0001t0001g0320 a0001c0001t0001g0321 others(6): Show |
9 | HG00741.hp2 HG01255.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.-71+233G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11762538 | |||||||
chr1:11762677 | A | G | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(224): Show |
242 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.-71+372A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11762677 | |||||||
chr1:11762687 | A | T | 1 | a0042c0040t0001g0317 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-71+382A>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11762687 | |||||||
chr1:11762833 | C | G | 1 | a0004c0007t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-71+528C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11762833 | |||||||
chr1:11762949 | T | C | 29 | a0001c0001t0001g0127 a0001c0009t0001g0126 a0001c0009t0001g0128 others(26): Show |
29 | HG01167.hp2 HG01891.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.-71+644T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11762949 | |||||||
chr1:11762986 | G | A | 1 | a0006c0005t0001g0026 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-71+681G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11762986 | |||||||
chr1:11763078 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-71+773T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763078 | |||||||
chr1:11763099 | A | G | 95 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(92): Show |
100 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-71+794A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763099 | |||||||
chr1:11763113 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-71+808T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763113 | |||||||
chr1:11763116 | G | A | 1 | a0016c0018t0001g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-71+811G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763116 | |||||||
chr1:11763123 | C | T | 2 | a0006c0005t0001g0025 a0015c0012t0001g0094 |
2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-71+818C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763123 | |||||||
chr1:11763216 | A | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.-71+911A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763216 | |||||||
chr1:11763238 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0274 |
2 | HG00673.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.-71+933G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763238 | |||||||
chr1:11763270 | T | C | 12 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0130 others(9): Show |
12 | HG00597.hp1 HG01081.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-71+965T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763270 | |||||||
chr1:11763402 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-70-929G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763402 | |||||||
chr1:11763442 | CA | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.-70-872delA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr1 | 11763442 | ||||||
chr1:11763461 | G | T | 7 | a0004c0007t0001g0062 a0006c0005t0001g0025 a0006c0005t0001g0101 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70-870G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763461 | |||||||
chr1:11763466 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-70-865G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763466 | |||||||
chr1:11763525 | C | T | 11 | a0004c0007t0001g0041 a0004c0007t0001g0100 a0004c0007t0001g0112 others(8): Show |
11 | HG01891.hp1 HG02717.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-70-806C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763525 | |||||||
chr1:11763538 | G | T | 1 | a0041c0058t0001g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-70-793G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763538 | |||||||
chr1:11763649 | G | C | 2 | a0002c0002t0001g0131 a0002c0002t0001g0171 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-70-682G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763649 | |||||||
chr1:11763723 | T | C | 1 | a0027c0022t0001g0198 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-70-608T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763723 | |||||||
chr1:11763738 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-70-593C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763738 | |||||||
chr1:11763750 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-70-581C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11763750 | |||||||
chr1:11764020 | A | G | 1 | a0008c0006t0001g0316 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-70-311A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11764020 | |||||||
chr1:11764076 | A | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
223 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.-70-255A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11764076 | |||||||
chr1:11764121 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-70-210G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11764121 | |||||||
chr1:11764185 | A | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
230 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.-70-146A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11764185 | |||||||
chr1:11764203 | T | C | 5 | a0016c0018t0001g0028 a0016c0018t0001g0051 a0016c0018t0001g0155 others(2): Show |
5 | HG00438.hp1 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70-128T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11764203 | |||||||
chr1:11764246 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
214 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.-70-85T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11764246 | |||||||
chr1:11764289 | G | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
207 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.-70-42G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 1/20 | chr1 | 11764289 | |||||||
chr1:11764499 | A | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
205 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.70+29A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764499 | |||||||
chr1:11764518 | T | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
275 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.70+48T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764518 | |||||||
chr1:11764519 | C | A | 2 | a0016c0018t0001g0028 a0016c0018t0001g0051 |
2 | HG02145.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.70+49C>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764519 | |||||||
chr1:11764521 | C | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
205 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.70+51C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764521 | |||||||
chr1:11764564 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
213 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.70+94T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764564 | |||||||
chr1:11764614 | G | C | 1 | a0001c0001t0001g0210 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.70+144G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764614 | |||||||
chr1:11764616 | A | T | 1 | a0002c0002t0001g0203 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.70+146A>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764616 | |||||||
chr1:11764619 | G | C | 8 | a0004c0017t0001g0044 a0004c0017t0001g0046 a0009c0008t0001g0114 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+149G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764619 | |||||||
chr1:11764636 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.70+166G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764636 | |||||||
chr1:11764858 | C | T | 1 | a0019c0061t0001g0319 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.70+388C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764858 | |||||||
chr1:11764870 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.70+400T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764870 | |||||||
chr1:11764957 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.70+487A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764957 | |||||||
chr1:11764985 | C | T | 1 | a0037c0060t0003g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.70+515C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11764985 | |||||||
chr1:11765002 | C | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
233 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.70+532C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11765002 | |||||||
chr1:11765030 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.70+560A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11765030 | |||||||
chr1:11765053 | C | CA | 22 | a0001c0001t0001g0165 a0001c0001t0001g0272 a0001c0001t0001g0315 others(19): Show |
22 | HG01993.hp2 HG02257.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.70+607dupA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | 11765053 | ||||||
chr1:11765053 | C | CAA | 131 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(128): Show |
135 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.70+606_70+607dupAA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | 11765053 | ||||||
chr1:11765053 | C | CAAA | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(81): Show |
92 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.70+605_70+607dupAA others(1): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | 11765053 | ||||||
chr1:11765053 | C | CAAAA | 19 | a0001c0001t0001g0079 a0001c0001t0001g0187 a0001c0001t0001g0212 others(16): Show |
19 | HG02109.hp1 HG02572.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.70+604_70+607dupAA others(2): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | 11765053 | ||||||
chr1:11765053 | C | CAAAAA | 5 | a0006c0005t0001g0012 a0006c0005t0001g0125 a0006c0005t0002g0020 others(2): Show |
6 | HG02647.hp1 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+603_70+607dupAA others(3): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | 11765053 | ||||||
chr1:11765053 | CA | C | 13 | a0002c0002t0001g0138 a0002c0002t0001g0174 a0002c0002t0001g0200 others(10): Show |
13 | HG02055.hp2 HG02056.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.70+607delA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | 11765053 | ||||||
chr1:11765053 | CAA | C | 35 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(32): Show |
41 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.70+606_70+607delAA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | 11765053 | ||||||
chr1:11765107 | G | T | 1 | a0037c0060t0003g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.70+637G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11765107 | |||||||
chr1:11765159 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70+689T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11765159 | |||||||
chr1:11765161 | G | A | 1 | a0037c0060t0003g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.70+691G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11765161 | |||||||
chr1:11765485 | C | CT | 6 | a0021c0016t0001g0197 a0021c0016t0001g0276 a0021c0016t0001g0289 others(3): Show |
6 | HG00438.hp1 HG03491.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-363dupT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | 11765485 | ||||||
chr1:11765486 | T | TTTTC | 5 | a0014c0015t0001g0017 a0014c0015t0001g0115 a0014c0015t0001g0116 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-368_71-367insCT others(2): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | 11765486 | ||||||
chr1:11765487 | T | C | 37 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(34): Show |
38 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.71-370T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11765487 | |||||||
chr1:11765506 | C | G | 12 | a0009c0008t0001g0042 a0009c0008t0001g0043 a0009c0008t0001g0136 others(9): Show |
12 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-351C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11765506 | |||||||
chr1:11765583 | C | CA | 212 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(209): Show |
224 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.71-273dupA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr1 | 11765583 | ||||||
chr1:11765684 | G | A | 1 | a0002c0002t0001g0175 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.71-173G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11765684 | |||||||
chr1:11765794 | G | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
221 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.71-63G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 2/20 | chr1 | 11765794 | |||||||
chr1:11767123 | A | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(316): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1299+38A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 3/20 | chr1 | 11767123 | |||||||
chr1:11767298 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(194): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1343+34A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 4/20 | chr1 | 11767298 | |||||||
chr1:11767717 | G | A | 4 | a0014c0015t0001g0017 a0014c0015t0001g0115 a0014c0015t0001g0116 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344-360G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 4/20 | chr1 | 11767717 | |||||||
chr1:11767719 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(209): Show |
224 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.1344-358A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 4/20 | chr1 | 11767719 | |||||||
chr1:11767739 | T | C | 7 | a0007c0010t0001g0035 a0007c0010t0001g0049 a0007c0010t0001g0050 others(4): Show |
7 | HG00099.hp1 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344-338T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 4/20 | chr1 | 11767739 | |||||||
chr1:11767759 | G | A | 1 | a0037c0060t0003g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1344-318G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 4/20 | chr1 | 11767759 | |||||||
chr1:11767775 | G | A | 319 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(316): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1344-302G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 4/20 | chr1 | 11767775 | |||||||
chr1:11767961 | G | A | 1 | a0037c0060t0003g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1344-116G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 4/20 | chr1 | 11767961 | |||||||
chr1:11768025 | C | T | 1 | a0019c0061t0001g0319 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1344-52C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 4/20 | chr1 | 11768025 | |||||||
chr1:11768307 | G | A | 42 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(39): Show |
43 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1542+32G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/20 | chr1 | 11768307 | |||||||
chr1:11768528 | C | T | 1 | a0037c0060t0003g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1542+253C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/20 | chr1 | 11768528 | |||||||
chr1:11768710 | G | A | 4 | a0013c0014t0001g0022 a0013c0014t0001g0047 a0013c0014t0001g0118 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-263G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/20 | chr1 | 11768710 | |||||||
chr1:11768721 | G | T | 4 | a0013c0014t0001g0022 a0013c0014t0001g0047 a0013c0014t0001g0118 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-252G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/20 | chr1 | 11768721 | |||||||
chr1:11768722 | C | T | 4 | a0013c0014t0001g0022 a0013c0014t0001g0047 a0013c0014t0001g0118 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-251C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/20 | chr1 | 11768722 | |||||||
chr1:11768766 | T | C | 1 | a0009c0008t0001g0122 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1543-207T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/20 | chr1 | 11768766 | |||||||
chr1:11768890 | C | G | 17 | a0009c0008t0001g0042 a0009c0008t0001g0043 a0009c0008t0001g0048 others(14): Show |
17 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1543-83C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/20 | chr1 | 11768890 | |||||||
chr1:11768939 | C | T | 4 | a0013c0014t0001g0022 a0013c0014t0001g0047 a0013c0014t0001g0118 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543-34C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/20 | chr1 | 11768939 | |||||||
chr1:11768955 | C | G | 1 | a0001c0045t0001g0249 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1543-18C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 5/20 | chr1 | 11768955 | |||||||
chr1:11769309 | G | A | 1 | a0007c0010t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1697+182G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11769309 | |||||||
chr1:11769475 | G | A | 5 | a0013c0014t0001g0022 a0013c0014t0001g0047 a0013c0014t0001g0118 others(2): Show |
5 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1697+348G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11769475 | |||||||
chr1:11769553 | T | G | 319 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(316): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1697+426T>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11769553 | |||||||
chr1:11769674 | G | GT | 242 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1697+562dupT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11769674 | ||||||
chr1:11769674 | G | GTT | 27 | a0001c0001t0001g0054 a0001c0001t0001g0110 a0001c0001t0001g0213 others(24): Show |
27 | HG00621.hp1 HG00741.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.1697+561_1697+562d others(4): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11769674 | ||||||
chr1:11769674 | G | GTTT | 34 | a0002c0002t0001g0097 a0003c0003t0001g0010 a0003c0003t0001g0075 others(31): Show |
35 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.1697+560_1697+562d others(5): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11769674 | ||||||
chr1:11769740 | C | T | 39 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(36): Show |
45 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1697+613C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11769740 | |||||||
chr1:11769741 | A | G | 43 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(40): Show |
49 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1697+614A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11769741 | |||||||
chr1:11769980 | A | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0001t0001g0189 others(1): Show |
4 | HG01243.hp2 HG03139.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1697+853A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11769980 | |||||||
chr1:11770012 | A | T | 1 | a0005c0004t0001g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1697+885A>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770012 | |||||||
chr1:11770037 | G | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0246 |
2 | NA18945.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1697+910G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770037 | |||||||
chr1:11770112 | T | C | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1697+985T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770112 | |||||||
chr1:11770123 | A | T | 45 | a0002c0002t0001g0001 a0002c0002t0001g0181 a0002c0002t0001g0200 others(42): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1697+996A>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770123 | |||||||
chr1:11770151 | T | TTAAATTT others(2161): Show |
1 | a0003c0003t0001g0075 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2172): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2160): Show |
1 | a0039c0043t0002g0021 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2171): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2160): Show |
1 | a0007c0057t0003g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2171): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2161): Show |
2 | a0003c0003t0001g0111 a0003c0003t0001g0166 |
2 | HG00609.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1697+1036_1697+103 others(2172): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2162): Show |
11 | a0003c0003t0001g0010 a0003c0003t0001g0105 a0003c0003t0001g0204 others(8): Show |
12 | HG00609.hp2 HG02040.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.1697+1036_1697+103 others(2173): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2163): Show |
1 | a0022c0028t0001g0248 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2174): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2164): Show |
1 | a0003c0003t0001g0300 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2175): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2162): Show |
1 | a0003c0003t0001g0283 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2173): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2163): Show |
1 | a0003c0003t0001g0306 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2174): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2163): Show |
1 | a0003c0003t0001g0284 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2174): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2164): Show |
1 | a0048c0042t0001g0299 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2175): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2164): Show |
1 | a0025c0023t0001g0262 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2175): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2163): Show |
1 | a0003c0003t0001g0307 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2174): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2167): Show |
1 | a0003c0003t0001g0277 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2178): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2167): Show |
1 | a0003c0003t0001g0258 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2178): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2160): Show |
3 | a0007c0010t0001g0049 a0007c0010t0001g0050 a0035c0062t0001g0260 |
3 | HG00099.hp1 HG02109.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1697+1036_1697+103 others(2171): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2161): Show |
1 | a0007c0010t0001g0172 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2172): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2160): Show |
1 | a0007c0010t0001g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2171): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2161): Show |
1 | a0037c0060t0003g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2172): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2161): Show |
1 | a0007c0010t0001g0173 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2172): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2164): Show |
1 | a0007c0010t0001g0199 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2175): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2163): Show |
1 | a0007c0010t0001g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2174): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770151 | T | TTAAATTT others(2163): Show |
1 | a0003c0003t0001g0208 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1697+1036_1697+103 others(2174): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770151 | ||||||
chr1:11770251 | G | GA | 10 | a0007c0050t0001g0119 a0012c0013t0001g0120 a0012c0013t0002g0030 others(7): Show |
10 | HG01109.hp2 HG01891.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1697+1135dupA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770251 | ||||||
chr1:11770364 | G | A | 5 | a0021c0016t0001g0197 a0021c0016t0001g0276 a0021c0016t0001g0289 others(2): Show |
5 | HG03491.hp1 NA18971.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.1698-1160G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770364 | |||||||
chr1:11770419 | G | A | 5 | a0021c0016t0001g0197 a0021c0016t0001g0276 a0021c0016t0001g0289 others(2): Show |
5 | HG03491.hp1 NA18971.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.1698-1105G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770419 | |||||||
chr1:11770449 | C | CT | 188 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
199 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1698-1062dupT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770449 | ||||||
chr1:11770449 | CT | C | 7 | a0002c0002t0001g0003 a0021c0016t0001g0197 a0021c0016t0001g0276 others(4): Show |
9 | HG01099.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1698-1062delT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770449 | ||||||
chr1:11770485 | G | T | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1698-1039G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770485 | |||||||
chr1:11770529 | C | T | 11 | a0009c0008t0001g0042 a0009c0008t0001g0043 a0009c0008t0001g0048 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1698-995C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770529 | |||||||
chr1:11770601 | G | A | 2 | a0003c0003t0001g0297 a0003c0003t0001g0298 |
2 | HG02080.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1698-923G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770601 | |||||||
chr1:11770610 | A | AT | 39 | a0001c0001t0001g0245 a0001c0001t0001g0259 a0002c0002t0001g0104 others(36): Show |
40 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1698-899dupT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770610 | ||||||
chr1:11770610 | AT | A | 24 | a0001c0001t0001g0301 a0009c0008t0001g0042 a0009c0008t0001g0043 others(21): Show |
24 | HG00438.hp1 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1698-899delT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770610 | ||||||
chr1:11770610 | ATT | A | 9 | a0007c0050t0001g0119 a0012c0013t0001g0120 a0012c0013t0002g0030 others(6): Show |
9 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1698-900_1698-899d others(4): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770610 | ||||||
chr1:11770741 | C | T | 3 | a0001c0009t0001g0006 a0001c0009t0001g0053 a0001c0009t0001g0126 |
4 | HG01192.hp1 HG02451.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1698-783C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770741 | |||||||
chr1:11770810 | A | AT | 6 | a0013c0014t0001g0022 a0013c0014t0001g0047 a0013c0014t0001g0118 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1698-701dupT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770810 | ||||||
chr1:11770810 | AT | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
203 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1698-701delT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770810 | ||||||
chr1:11770829 | G | C | 1 | a0036c0032t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1698-695G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770829 | |||||||
chr1:11770866 | G | A | 43 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(40): Show |
49 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1698-658G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11770866 | |||||||
chr1:11770972 | T | TTG | 8 | a0004c0007t0001g0062 a0004c0007t0001g0112 a0012c0013t0002g0147 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1698-524_1698-523d others(4): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770972 | ||||||
chr1:11770972 | T | TTGTG | 3 | a0004c0007t0001g0041 a0004c0007t0001g0150 a0004c0017t0001g0046 |
3 | HG01243.hp1 HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1698-526_1698-523d others(6): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770972 | ||||||
chr1:11770972 | T | TTGTGTG | 11 | a0009c0008t0001g0042 a0009c0008t0001g0043 a0009c0008t0001g0048 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1698-528_1698-523d others(8): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770972 | ||||||
chr1:11770972 | TTG | T | 4 | a0002c0002t0001g0131 a0002c0002t0001g0171 a0029c0033t0001g0291 others(1): Show |
4 | HG00438.hp1 HG01168.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1698-524_1698-523d others(4): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770972 | ||||||
chr1:11770972 | TTGTG | T | 44 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(41): Show |
50 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.1698-526_1698-523d others(6): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770972 | ||||||
chr1:11770972 | TTGTGTGT others(1): Show |
T | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1698-530_1698-523d others(10): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770972 | ||||||
chr1:11770992 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0001g0259 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1698-530_1698-521d others(12): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770992 | ||||||
chr1:11770994 | GTGTGTGT others(1): Show |
G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(157): Show |
170 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.1698-528_1698-521d others(10): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770994 | ||||||
chr1:11770996 | GTGTGTA | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0073 others(13): Show |
17 | HG00140.hp1 HG00323.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.1698-526_1698-521d others(8): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770996 | ||||||
chr1:11770998 | GTGTA | G | 3 | a0014c0015t0001g0017 a0014c0015t0001g0133 a0021c0016t0001g0276 |
3 | HG02258.hp1 HG02280.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1698-524_1698-521d others(6): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11770998 | ||||||
chr1:11771000 | GTA | G | 22 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(19): Show |
22 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1698-518_1698-517d others(4): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771000 | ||||||
chr1:11771002 | A | G | 4 | a0007c0050t0001g0119 a0012c0013t0002g0147 a0032c0047t0001g0063 others(1): Show |
4 | HG01109.hp2 HG01884.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1698-522A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771002 | |||||||
chr1:11771004 | A | G | 14 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.1698-520A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771004 | |||||||
chr1:11771021 | G | A | 1 | a0012c0013t0002g0147 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1698-503G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771021 | |||||||
chr1:11771031 | A | ATG | 4 | a0002c0002t0001g0176 a0003c0003t0001g0297 a0007c0010t0001g0035 others(1): Show |
4 | HG02055.hp1 HG02080.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1698-475_1698-474d others(4): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771031 | ||||||
chr1:11771031 | A | ATGTGTG | 3 | a0003c0003t0001g0263 a0003c0003t0001g0298 a0035c0062t0001g0260 |
3 | HG02109.hp2 HG02165.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1698-479_1698-474d others(8): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771031 | ||||||
chr1:11771031 | A | ATGTGTGT others(1): Show |
22 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(19): Show |
23 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1698-481_1698-474d others(10): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771031 | ||||||
chr1:11771031 | A | G | 1 | a0003c0003t0001g0208 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1698-493A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771031 | |||||||
chr1:11771031 | ATG | A | 22 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(19): Show |
22 | HG00323.hp1 HG00597.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1698-475_1698-474d others(4): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771031 | ||||||
chr1:11771031 | ATGTG | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0057 others(43): Show |
48 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1698-477_1698-474d others(6): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771031 | ||||||
chr1:11771045 | G | A | 21 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(18): Show |
21 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.1698-479G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771045 | |||||||
chr1:11771047 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
148 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.1698-477G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771047 | |||||||
chr1:11771049 | G | A | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
190 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1698-475G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771049 | |||||||
chr1:11771049 | G | GTGTGTGT others(11): Show |
1 | a0022c0028t0001g0271 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1698-474_1698-473i others(20): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771049 | ||||||
chr1:11771051 | A | G | 78 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(75): Show |
84 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1698-473A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771051 | |||||||
chr1:11771053 | A | G | 54 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(51): Show |
60 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1698-471A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771053 | |||||||
chr1:11771055 | A | G | 51 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(48): Show |
57 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1698-469A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771055 | |||||||
chr1:11771057 | A | G | 12 | a0002c0002t0001g0007 a0002c0002t0001g0143 a0002c0002t0001g0171 others(9): Show |
13 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1698-467A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771057 | |||||||
chr1:11771064 | TATA | T | 5 | a0001c0001t0001g0226 a0001c0001t0001g0305 a0001c0001t0001g0313 others(2): Show |
5 | HG02630.hp1 NA18966.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1698-459_1698-457d others(5): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771064 | |||||||
chr1:11771066 | TATA | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0107 others(16): Show |
19 | HG01123.hp2 HG01258.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1698-457_1698-455d others(5): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771066 | |||||||
chr1:11771067 | ATAT | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
68 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1698-455_1698-453d others(5): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771067 | ||||||
chr1:11771069 | A | ATATATAT others(8): Show |
1 | a0052c0049t0001g0230 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1698-454_1698-453i others(17): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771069 | ||||||
chr1:11771069 | A | ATATATAT others(11): Show |
1 | a0029c0033t0001g0291 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1698-454_1698-453i others(20): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771069 | ||||||
chr1:11771069 | A | ATATATAT others(3): Show |
1 | a0005c0004t0001g0064 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1698-454_1698-453i others(12): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771069 | ||||||
chr1:11771069 | A | ATATATTT | 6 | a0005c0004t0001g0144 a0005c0004t0001g0145 a0005c0004t0001g0254 others(3): Show |
6 | HG00642.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1698-454_1698-453i others(9): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771069 | ||||||
chr1:11771069 | A | T | 12 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0103 others(9): Show |
12 | HG00544.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1698-455A>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771069 | |||||||
chr1:11771069 | AT | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0130 a0001c0001t0001g0214 others(11): Show |
14 | HG02109.hp2 HG02559.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1698-428delT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771069 | ||||||
chr1:11771069 | ATTT | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0087 others(15): Show |
20 | HG00140.hp1 HG00673.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1698-430_1698-428d others(5): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771069 | ||||||
chr1:11771069 | ATTTTTTT others(3): Show |
A | 1 | a0004c0007t0001g0252 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1698-437_1698-428d others(12): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771069 | ||||||
chr1:11771070 | T | TA | 32 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0069 others(29): Show |
37 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1698-454_1698-453i others(3): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771070 | |||||||
chr1:11771070 | T | TATA | 20 | a0002c0002t0001g0007 a0002c0002t0001g0138 a0002c0002t0001g0140 others(17): Show |
21 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1698-454_1698-453i others(5): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771070 | |||||||
chr1:11771070 | T | TATATA | 4 | a0009c0008t0001g0042 a0009c0008t0001g0048 a0009c0008t0001g0122 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1698-454_1698-453i others(7): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771070 | |||||||
chr1:11771070 | T | TATATATA others(8): Show |
1 | a0009c0008t0001g0136 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1698-454_1698-453i others(17): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771070 | |||||||
chr1:11771071 | T | A | 69 | a0001c0001t0001g0057 a0001c0001t0001g0080 a0001c0001t0001g0091 others(66): Show |
70 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1698-453T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771071 | |||||||
chr1:11771072 | T | A | 59 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(56): Show |
65 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1698-452T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771072 | |||||||
chr1:11771073 | T | A | 36 | a0001c0001t0001g0080 a0001c0001t0001g0215 a0001c0001t0001g0274 others(33): Show |
37 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1698-451T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771073 | |||||||
chr1:11771074 | T | A | 62 | a0001c0001t0001g0308 a0002c0002t0001g0001 a0002c0002t0001g0003 others(59): Show |
68 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.1698-450T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771074 | |||||||
chr1:11771075 | T | A | 30 | a0002c0002t0001g0176 a0002c0002t0001g0177 a0003c0003t0001g0010 others(27): Show |
31 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1698-449T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771075 | |||||||
chr1:11771076 | T | A | 57 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(54): Show |
63 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1698-448T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771076 | |||||||
chr1:11771077 | T | A | 26 | a0002c0002t0001g0176 a0003c0003t0001g0010 a0003c0003t0001g0105 others(23): Show |
27 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.1698-447T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771077 | |||||||
chr1:11771078 | T | A | 17 | a0002c0002t0001g0181 a0003c0003t0001g0075 a0003c0003t0001g0204 others(14): Show |
17 | HG00741.hp1 HG01884.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.1698-446T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771078 | |||||||
chr1:11771079 | T | A | 24 | a0003c0003t0001g0010 a0003c0003t0001g0105 a0003c0003t0001g0111 others(21): Show |
25 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.1698-445T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771079 | |||||||
chr1:11771080 | T | A | 13 | a0003c0003t0001g0075 a0003c0003t0001g0204 a0003c0003t0001g0296 others(10): Show |
13 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1698-444T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771080 | |||||||
chr1:11771081 | T | A | 23 | a0003c0003t0001g0010 a0003c0003t0001g0105 a0003c0003t0001g0111 others(20): Show |
24 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.1698-443T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771081 | |||||||
chr1:11771082 | T | A | 6 | a0003c0003t0001g0075 a0003c0003t0001g0204 a0003c0003t0001g0296 others(3): Show |
6 | HG01884.hp2 HG03130.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1698-442T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771082 | |||||||
chr1:11771151 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0187 |
2 | NA18986.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1698-373T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771151 | |||||||
chr1:11771187 | C | G | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1698-337C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771187 | |||||||
chr1:11771200 | T | G | 1 | a0001c0001t0001g0312 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1698-324T>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771200 | |||||||
chr1:11771203 | G | A | 1 | a0033c0056t0001g0085 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1698-321G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771203 | |||||||
chr1:11771246 | G | T | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1698-278G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771246 | |||||||
chr1:11771297 | T | TA | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1698-220dupA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr1 | 11771297 | ||||||
chr1:11771359 | C | T | 5 | a0007c0050t0001g0119 a0012c0013t0001g0120 a0012c0013t0002g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1698-165C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771359 | |||||||
chr1:11771387 | C | T | 5 | a0013c0014t0001g0022 a0013c0014t0001g0047 a0013c0014t0001g0118 others(2): Show |
5 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1698-137C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771387 | |||||||
chr1:11771435 | C | T | 1 | a0003c0003t0001g0306 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1698-89C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771435 | |||||||
chr1:11771455 | C | T | 9 | a0002c0002t0001g0184 a0009c0008t0001g0042 a0009c0008t0001g0043 others(6): Show |
9 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1698-69C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771455 | |||||||
chr1:11771486 | C | T | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1698-38C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 6/20 | chr1 | 11771486 | |||||||
chr1:11771688 | G | T | 1 | a0021c0016t0001g0276 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1810+52G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 7/20 | chr1 | 11771688 | |||||||
chr1:11771699 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
236 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1810+63A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 7/20 | chr1 | 11771699 | |||||||
chr1:11771818 | A | G | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1810+182A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 7/20 | chr1 | 11771818 | |||||||
chr1:11772043 | T | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
189 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.1811-39T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 7/20 | chr1 | 11772043 | |||||||
chr1:11772311 | G | C | 3 | a0023c0025t0001g0196 a0023c0025t0001g0250 a0049c0038t0001g0077 |
3 | HG02293.hp1 HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1988+52G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11772311 | |||||||
chr1:11772413 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1988+154T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11772413 | |||||||
chr1:11772431 | AT | A | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
235 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1988+179delT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772431 | ||||||
chr1:11772474 | C | G | 1 | a0032c0047t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1988+215C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11772474 | |||||||
chr1:11772554 | A | C | 1 | a0032c0047t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1988+295A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11772554 | |||||||
chr1:11772566 | C | G | 20 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(17): Show |
20 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1988+307C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11772566 | |||||||
chr1:11772602 | A | G | 40 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(37): Show |
46 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.1988+343A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11772602 | |||||||
chr1:11772655 | C | G | 1 | a0032c0047t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1988+396C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11772655 | |||||||
chr1:11772730 | C | T | 5 | a0021c0016t0001g0197 a0021c0016t0001g0276 a0021c0016t0001g0289 others(2): Show |
5 | HG03491.hp1 NA18971.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988+471C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11772730 | |||||||
chr1:11772839 | A | C | 1 | a0032c0047t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1988+580A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11772839 | |||||||
chr1:11772855 | C | CT | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1988+603dupT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772855 | ||||||
chr1:11772864 | C | T | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1988+605C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11772864 | |||||||
chr1:11772894 | C | CATTATTA others(8): Show |
23 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(20): Show |
24 | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1988+642_1988+656d others(17): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772894 | ||||||
chr1:11772894 | C | CATTATTA others(11): Show |
8 | a0003c0003t0001g0277 a0007c0010t0001g0035 a0007c0050t0001g0119 others(5): Show |
8 | HG00597.hp1 HG01109.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1988+639_1988+656d others(20): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772894 | ||||||
chr1:11772894 | C | CATTATTA others(14): Show |
7 | a0007c0010t0001g0049 a0007c0010t0001g0172 a0007c0010t0001g0173 others(4): Show |
7 | HG02109.hp2 HG02132.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1988+636_1988+656d others(23): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772894 | ||||||
chr1:11772894 | C | CATTATTA others(17): Show |
5 | a0007c0010t0001g0050 a0007c0010t0001g0199 a0007c0057t0003g0019 others(2): Show |
5 | HG00099.hp1 HG02258.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988+656_1988+657i others(26): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772894 | ||||||
chr1:11772894 | C | CATTATTA others(20): Show |
3 | a0001c0001t0001g0156 a0007c0010t0001g0039 a0014c0015t0001g0133 |
3 | HG01952.hp2 HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1988+656_1988+657i others(29): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772894 | ||||||
chr1:11772904 | A | ATTATTAT others(16): Show |
3 | a0001c0001t0001g0214 a0001c0001t0001g0220 a0001c0009t0001g0038 |
3 | HG02451.hp2 NA18968.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1988+656_1988+657i others(25): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772904 | ||||||
chr1:11772904 | A | ATTATTAT others(19): Show |
87 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(84): Show |
92 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1988+656_1988+657i others(28): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772904 | ||||||
chr1:11772904 | A | ATTATTAT others(22): Show |
72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(69): Show |
78 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1988+656_1988+657i others(31): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772904 | ||||||
chr1:11772904 | A | ATTATTAT others(25): Show |
14 | a0001c0001t0001g0054 a0001c0001t0001g0092 a0001c0001t0001g0110 others(11): Show |
14 | HG00544.hp2 HG00621.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.1988+656_1988+657i others(34): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772904 | ||||||
chr1:11772904 | A | ATTATTAT others(28): Show |
1 | a0001c0001t0001g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1988+656_1988+657i others(37): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11772904 | ||||||
chr1:11772930 | G | A | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1988+671G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11772930 | |||||||
chr1:11773038 | C | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
189 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.1988+779C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773038 | |||||||
chr1:11773058 | C | T | 1 | a0010c0011t0001g0135 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1988+799C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773058 | |||||||
chr1:11773081 | A | G | 3 | a0020c0024t0001g0132 a0020c0024t0001g0151 a0020c0035t0001g0040 |
3 | HG02965.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1988+822A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773081 | |||||||
chr1:11773090 | A | G | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
235 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1988+831A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773090 | |||||||
chr1:11773091 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1988+832G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773091 | |||||||
chr1:11773102 | T | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
235 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1988+843T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773102 | |||||||
chr1:11773247 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1988+988G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773247 | |||||||
chr1:11773289 | C | T | 9 | a0007c0050t0001g0119 a0012c0013t0001g0120 a0012c0013t0002g0030 others(6): Show |
9 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1988+1030C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773289 | |||||||
chr1:11773309 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
189 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.1988+1050A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773309 | |||||||
chr1:11773344 | T | C | 5 | a0021c0016t0001g0197 a0021c0016t0001g0276 a0021c0016t0001g0289 others(2): Show |
5 | HG03491.hp1 NA18971.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988+1085T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773344 | |||||||
chr1:11773384 | T | C | 2 | a0002c0002t0001g0131 a0002c0002t0001g0171 |
2 | HG01168.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1988+1125T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773384 | |||||||
chr1:11773434 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
198 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.1988+1175G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773434 | |||||||
chr1:11773436 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1988+1177G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773436 | |||||||
chr1:11773468 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
198 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.1988+1209G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773468 | |||||||
chr1:11773505 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1988+1246T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773505 | |||||||
chr1:11773650 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1988+1391G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773650 | |||||||
chr1:11773651 | T | A | 9 | a0007c0050t0001g0119 a0012c0013t0001g0120 a0012c0013t0002g0030 others(6): Show |
9 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1988+1392T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773651 | |||||||
chr1:11773663 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
198 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.1988+1404G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773663 | |||||||
chr1:11773695 | G | A | 5 | a0023c0025t0001g0196 a0023c0025t0001g0250 a0029c0033t0001g0291 others(2): Show |
5 | HG00438.hp1 HG02293.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1988+1436G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773695 | |||||||
chr1:11773795 | C | T | 5 | a0007c0050t0001g0119 a0012c0013t0001g0120 a0012c0013t0002g0030 others(2): Show |
5 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1988+1536C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773795 | |||||||
chr1:11773799 | C | T | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1988+1540C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773799 | |||||||
chr1:11773853 | A | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
198 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.1989-1582A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773853 | |||||||
chr1:11773885 | T | A | 1 | a0034c0030t0001g0076 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1989-1550T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773885 | |||||||
chr1:11773917 | A | AG | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1989-1518_1989-151 others(5): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773917 | |||||||
chr1:11773919 | A | AT | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
198 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.1989-1515dupT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11773919 | ||||||
chr1:11773919 | A | T | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1989-1516A>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11773919 | |||||||
chr1:11774050 | A | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
235 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1989-1385A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774050 | |||||||
chr1:11774106 | C | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
197 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.1989-1329C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774106 | |||||||
chr1:11774125 | G | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
189 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.1989-1310G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774125 | |||||||
chr1:11774130 | C | G | 1 | a0005c0004t0001g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1989-1305C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774130 | |||||||
chr1:11774147 | C | T | 1 | a0009c0008t0001g0042 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1989-1288C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774147 | |||||||
chr1:11774211 | A | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0318 |
2 | HG01261.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1989-1224A>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774211 | |||||||
chr1:11774255 | G | T | 3 | a0002c0002t0001g0202 a0002c0002t0001g0323 a0018c0019t0001g0093 |
3 | HG01074.hp2 HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1989-1180G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774255 | |||||||
chr1:11774397 | G | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
189 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.1989-1038G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774397 | |||||||
chr1:11774652 | G | A | 37 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(34): Show |
38 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1989-783G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774652 | |||||||
chr1:11774673 | G | T | 4 | a0014c0015t0001g0017 a0014c0015t0001g0115 a0014c0015t0001g0116 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1989-762G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774673 | |||||||
chr1:11774708 | A | G | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
235 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1989-727A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774708 | |||||||
chr1:11774713 | A | C | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG01255.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1989-722A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11774713 | |||||||
chr1:11775012 | C | T | 4 | a0012c0013t0001g0120 a0012c0013t0002g0030 a0012c0013t0002g0147 others(1): Show |
4 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1989-423C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11775012 | |||||||
chr1:11775013 | G | A | 37 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(34): Show |
38 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1989-422G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11775013 | |||||||
chr1:11775032 | T | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
235 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1989-403T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11775032 | |||||||
chr1:11775054 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(305): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1989-381A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11775054 | |||||||
chr1:11775130 | CA | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(212): Show |
227 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1989-296delA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr1 | 11775130 | ||||||
chr1:11775398 | T | G | 45 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(42): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1989-37T>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 8/20 | chr1 | 11775398 | |||||||
chr1:11775768 | G | C | 1 | a0001c0009t0001g0128 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2164+158G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11775768 | |||||||
chr1:11775878 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
237 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2164+268T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11775878 | |||||||
chr1:11775980 | C | T | 45 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(42): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.2164+370C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11775980 | |||||||
chr1:11776043 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2165-421G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11776043 | |||||||
chr1:11776043 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2165-421G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11776043 | |||||||
chr1:11776126 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
191 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.2165-338G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11776126 | |||||||
chr1:11776176 | G | A | 45 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(42): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.2165-288G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11776176 | |||||||
chr1:11776211 | C | T | 1 | a0032c0047t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2165-253C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11776211 | |||||||
chr1:11776258 | AAAGAAAC | A | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.2165-203_2165-197d others(9): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 11776258 | ||||||
chr1:11776261 | G | A | 272 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.2165-203G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11776261 | |||||||
chr1:11776273 | AAAAAAC | A | 9 | a0007c0010t0001g0035 a0007c0010t0001g0039 a0007c0010t0001g0049 others(6): Show |
9 | HG00099.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2165-185_2165-180d others(8): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr1 | 11776273 | ||||||
chr1:11776384 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(305): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.2165-80T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11776384 | |||||||
chr1:11776385 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
191 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.2165-79G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11776385 | |||||||
chr1:11776393 | A | G | 40 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(37): Show |
46 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.2165-71A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11776393 | |||||||
chr1:11776416 | G | T | 1 | a0013c0014t0001g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2165-48G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 9/20 | chr1 | 11776416 | |||||||
chr1:11776726 | G | A | 1 | a0003c0003t0001g0111 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2339+88G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11776726 | |||||||
chr1:11776754 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2339+116G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11776754 | |||||||
chr1:11776811 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
237 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2339+173A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11776811 | |||||||
chr1:11776829 | G | A | 1 | a0006c0005t0002g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2339+191G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11776829 | |||||||
chr1:11776907 | G | A | 1 | a0002c0002t0001g0069 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2339+269G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11776907 | |||||||
chr1:11776945 | C | A | 3 | a0021c0016t0001g0197 a0021c0016t0001g0276 a0021c0016t0001g0289 |
3 | HG03491.hp1 NA18986.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2339+307C>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11776945 | |||||||
chr1:11776987 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2339+349G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11776987 | |||||||
chr1:11776991 | C | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
237 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2339+353C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11776991 | |||||||
chr1:11776994 | C | T | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
237 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2339+356C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11776994 | |||||||
chr1:11777242 | A | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(305): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.2339+604A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777242 | |||||||
chr1:11777310 | C | T | 45 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(42): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.2339+672C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777310 | |||||||
chr1:11777416 | C | T | 37 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(34): Show |
38 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.2339+778C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777416 | |||||||
chr1:11777484 | C | G | 3 | a0007c0050t0001g0119 a0007c0057t0003g0019 a0039c0043t0002g0021 |
3 | HG02723.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2339+846C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777484 | |||||||
chr1:11777524 | G | A | 7 | a0007c0010t0001g0035 a0007c0010t0001g0049 a0007c0010t0001g0050 others(4): Show |
7 | HG00099.hp1 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2339+886G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777524 | |||||||
chr1:11777592 | A | C | 45 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(42): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.2339+954A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777592 | |||||||
chr1:11777625 | A | G | 45 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(42): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.2339+987A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777625 | |||||||
chr1:11777645 | C | CA | 40 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(37): Show |
41 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.2340-1001dupA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11777645 | ||||||
chr1:11777645 | CA | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
273 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.2340-1001delA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11777645 | ||||||
chr1:11777648 | A | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
191 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.2339+1010A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777648 | |||||||
chr1:11777700 | A | T | 45 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(42): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.2340-960A>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777700 | |||||||
chr1:11777701 | T | G | 18 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(15): Show |
18 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.2340-959T>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777701 | |||||||
chr1:11777750 | A | C | 1 | a0019c0061t0001g0319 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2340-910A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777750 | |||||||
chr1:11777812 | C | T | 8 | a0012c0013t0001g0120 a0012c0013t0002g0030 a0012c0013t0002g0147 others(5): Show |
8 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2340-848C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777812 | |||||||
chr1:11777954 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
237 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2340-706T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777954 | |||||||
chr1:11777999 | C | G | 2 | a0007c0010t0001g0039 a0037c0060t0003g0113 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2340-661C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11777999 | |||||||
chr1:11778042 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
237 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2340-618A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11778042 | |||||||
chr1:11778207 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
237 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2340-453A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11778207 | |||||||
chr1:11778291 | C | CA | 11 | a0004c0007t0001g0041 a0005c0004t0001g0064 a0005c0004t0001g0071 others(8): Show |
11 | HG00438.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2340-345dupA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11778291 | ||||||
chr1:11778291 | CA | C | 54 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(51): Show |
60 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.2340-345delA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11778291 | ||||||
chr1:11778291 | CAA | C | 32 | a0001c0001t0001g0016 a0001c0001t0001g0067 a0001c0001t0001g0079 others(29): Show |
35 | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2340-346_2340-345d others(4): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11778291 | ||||||
chr1:11778291 | CAAA | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
167 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.2340-347_2340-345d others(5): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11778291 | ||||||
chr1:11778291 | CAAAA | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0194 others(6): Show |
10 | HG02273.hp1 HG02273.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.2340-348_2340-345d others(6): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr1 | 11778291 | ||||||
chr1:11778321 | A | G | 45 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(42): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.2340-339A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11778321 | |||||||
chr1:11778371 | C | G | 1 | a0032c0047t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2340-289C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11778371 | |||||||
chr1:11778394 | C | T | 45 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(42): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.2340-266C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11778394 | |||||||
chr1:11778459 | C | T | 48 | a0001c0009t0001g0006 a0001c0009t0001g0053 a0001c0009t0001g0126 others(45): Show |
50 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.2340-201C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11778459 | |||||||
chr1:11778499 | G | C | 18 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(15): Show |
18 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.2340-161G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11778499 | |||||||
chr1:11778589 | A | C | 39 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(36): Show |
45 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.2340-71A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11778589 | |||||||
chr1:11778639 | A | G | 45 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(42): Show |
46 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.2340-21A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 10/20 | chr1 | 11778639 | |||||||
chr1:11779100 | C | T | 3 | a0002c0002t0001g0097 a0014c0015t0001g0115 a0014c0015t0001g0116 |
3 | HG03516.hp1 HG03579.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2651+20C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779100 | |||||||
chr1:11779130 | C | T | 8 | a0012c0013t0001g0120 a0012c0013t0002g0030 a0012c0013t0002g0147 others(5): Show |
8 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2651+50C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779130 | |||||||
chr1:11779134 | C | T | 3 | a0020c0024t0001g0132 a0020c0024t0001g0151 a0020c0035t0001g0040 |
3 | HG02965.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2651+54C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779134 | |||||||
chr1:11779144 | T | A | 46 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(43): Show |
47 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.2651+64T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779144 | |||||||
chr1:11779151 | C | T | 18 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(15): Show |
18 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.2651+71C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779151 | |||||||
chr1:11779169 | A | G | 9 | a0007c0010t0001g0035 a0007c0010t0001g0039 a0007c0010t0001g0049 others(6): Show |
9 | HG00099.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2651+89A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779169 | |||||||
chr1:11779223 | C | A | 1 | a0002c0002t0001g0069 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2651+143C>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779223 | |||||||
chr1:11779242 | C | T | 1 | a0046c0044t0001g0219 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2651+162C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779242 | |||||||
chr1:11779378 | T | C | 297 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(294): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2651+298T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779378 | |||||||
chr1:11779483 | CG | C | 8 | a0012c0013t0001g0120 a0012c0013t0002g0030 a0012c0013t0002g0147 others(5): Show |
8 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2652-317delG | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr1 | 11779483 | ||||||
chr1:11779619 | G | A | 1 | a0010c0011t0001g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2652-183G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779619 | |||||||
chr1:11779674 | A | G | 1 | a0032c0047t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2652-128A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779674 | |||||||
chr1:11779735 | T | C | 46 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(43): Show |
47 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.2652-67T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | chr1 | 11779735 | |||||||
chr1:11779793 | CT | C | 39 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(36): Show |
45 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
splice_region_variant&intron_variant | LOW | c.2652-6delT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr1 | 11779793 | ||||||
chr1:11780126 | G | A | 3 | a0001c0009t0001g0006 a0001c0009t0001g0053 a0001c0009t0001g0126 |
4 | HG01192.hp1 HG02451.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2860+116G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11780126 | |||||||
chr1:11780323 | A | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
190 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.2860+313A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11780323 | |||||||
chr1:11780371 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(305): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.2860+361A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11780371 | |||||||
chr1:11780410 | C | T | 18 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(15): Show |
18 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.2860+400C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11780410 | |||||||
chr1:11780426 | G | A | 6 | a0023c0025t0001g0196 a0023c0025t0001g0250 a0029c0033t0001g0291 others(3): Show |
6 | HG00438.hp1 HG02293.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.2860+416G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11780426 | |||||||
chr1:11780426 | G | C | 264 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.2860+416G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11780426 | |||||||
chr1:11780468 | G | C | 4 | a0014c0015t0001g0017 a0014c0015t0001g0115 a0014c0015t0001g0116 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2860+458G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11780468 | |||||||
chr1:11780717 | A | C | 1 | a0003c0003t0001g0297 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2860+707A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11780717 | |||||||
chr1:11780805 | G | A | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(222): Show |
237 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2860+795G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11780805 | |||||||
chr1:11780816 | G | T | 11 | a0009c0008t0001g0042 a0009c0008t0001g0043 a0009c0008t0001g0048 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2860+806G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11780816 | |||||||
chr1:11780886 | T | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
190 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.2860+876T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11780886 | |||||||
chr1:11780921 | GAGGGATG others(5): Show |
G | 46 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(43): Show |
47 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.2860+913_2860+924d others(14): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 11780921 | ||||||
chr1:11780999 | C | CT | 14 | a0002c0002t0001g0069 a0002c0002t0001g0141 a0002c0002t0001g0174 others(11): Show |
14 | HG00642.hp2 HG02602.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2860+1011dupT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 11780999 | ||||||
chr1:11780999 | C | CTTT | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
163 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.2860+1009_2860+101 others(7): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 11780999 | ||||||
chr1:11780999 | C | CTTTT | 34 | a0001c0001t0001g0054 a0001c0001t0001g0080 a0001c0001t0001g0088 others(31): Show |
34 | HG00438.hp2 HG00621.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.2860+1008_2860+101 others(8): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 11780999 | ||||||
chr1:11780999 | CT | C | 20 | a0012c0013t0001g0120 a0012c0013t0002g0030 a0012c0013t0002g0147 others(17): Show |
20 | HG00323.hp2 HG01109.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2860+1011delT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 11780999 | ||||||
chr1:11781067 | G | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
190 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.2860+1057G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781067 | |||||||
chr1:11781085 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2860+1075C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781085 | |||||||
chr1:11781124 | C | T | 1 | a0010c0011t0001g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2861-1065C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781124 | |||||||
chr1:11781294 | G | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
190 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.2861-895G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781294 | |||||||
chr1:11781309 | C | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
190 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.2861-880C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781309 | |||||||
chr1:11781453 | T | C | 5 | a0013c0014t0001g0022 a0013c0014t0001g0047 a0013c0014t0001g0118 others(2): Show |
5 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2861-736T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781453 | |||||||
chr1:11781466 | C | T | 3 | a0021c0016t0001g0197 a0021c0016t0001g0276 a0021c0016t0001g0289 |
3 | HG03491.hp1 NA18986.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2861-723C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781466 | |||||||
chr1:11781632 | C | T | 39 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(36): Show |
45 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.2861-557C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781632 | |||||||
chr1:11781633 | G | A | 1 | a0003c0003t0001g0207 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2861-556G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781633 | |||||||
chr1:11781706 | C | T | 1 | a0001c0009t0001g0128 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2861-483C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781706 | |||||||
chr1:11781708 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0222 |
2 | HG00558.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2861-481A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781708 | |||||||
chr1:11781738 | G | A | 4 | a0012c0013t0001g0120 a0012c0013t0002g0030 a0012c0013t0002g0147 others(1): Show |
4 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2861-451G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781738 | |||||||
chr1:11781783 | G | A | 1 | a0032c0047t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2861-406G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781783 | |||||||
chr1:11781824 | G | A | 46 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(43): Show |
47 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.2861-365G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781824 | |||||||
chr1:11781852 | G | A | 39 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(36): Show |
45 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.2861-337G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781852 | |||||||
chr1:11781864 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(305): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.2861-325T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781864 | |||||||
chr1:11781865 | G | A | 46 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(43): Show |
47 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.2861-324G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781865 | |||||||
chr1:11781888 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(195): Show |
209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.2861-301T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781888 | |||||||
chr1:11781889 | G | A | 6 | a0001c0001t0001g0190 a0001c0001t0001g0226 a0001c0001t0001g0272 others(3): Show |
6 | NA18939.hp1 NA18966.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.2861-300G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781889 | |||||||
chr1:11781909 | CA | C | 91 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0002c0002t0001g0001 others(88): Show |
98 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.2861-265delA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr1 | 11781909 | ||||||
chr1:11781938 | T | G | 4 | a0014c0015t0001g0017 a0014c0015t0001g0115 a0014c0015t0001g0116 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2861-251T>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781938 | |||||||
chr1:11781988 | A | G | 1 | a0032c0047t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2861-201A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11781988 | |||||||
chr1:11782087 | C | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
190 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.2861-102C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11782087 | |||||||
chr1:11782157 | C | T | 1 | a0032c0047t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2861-32C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 13/20 | chr1 | 11782157 | |||||||
chr1:11782419 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3005+86C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11782419 | |||||||
chr1:11782434 | G | A | 39 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(36): Show |
45 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.3005+101G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11782434 | |||||||
chr1:11782606 | G | T | 1 | a0008c0006t0001g0206 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3005+273G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11782606 | |||||||
chr1:11782627 | A | G | 1 | a0003c0003t0001g0297 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3005+294A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11782627 | |||||||
chr1:11782667 | T | C | 5 | a0013c0014t0001g0022 a0013c0014t0001g0047 a0013c0014t0001g0118 others(2): Show |
5 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3005+334T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11782667 | |||||||
chr1:11782918 | C | G | 1 | a0048c0042t0001g0299 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3005+585C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11782918 | |||||||
chr1:11782918 | CA | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
251 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(248): Show |
intron_variant | MODIFIER | c.3005+603delA | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | 11782918 | ||||||
chr1:11782951 | C | A | 8 | a0012c0013t0001g0120 a0012c0013t0002g0030 a0012c0013t0002g0147 others(5): Show |
8 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3005+618C>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11782951 | |||||||
chr1:11782951 | CT | C | 38 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(35): Show |
39 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.3005+619delT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11782951 | |||||||
chr1:11783014 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3005+681A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783014 | |||||||
chr1:11783080 | A | G | 3 | a0004c0007t0001g0137 a0004c0007t0001g0252 a0041c0058t0001g0167 |
3 | HG02886.hp1 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3005+747A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783080 | |||||||
chr1:11783110 | A | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
190 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.3005+777A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783110 | |||||||
chr1:11783167 | C | T | 3 | a0002c0002t0001g0141 a0002c0002t0001g0174 a0002c0002t0001g0253 |
3 | HG02698.hp2 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3005+834C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783167 | |||||||
chr1:11783206 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3005+873C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783206 | |||||||
chr1:11783242 | TTTTG | T | 11 | a0009c0008t0001g0042 a0009c0008t0001g0043 a0009c0008t0001g0048 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.3006-916_3006-913d others(6): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | 11783242 | ||||||
chr1:11783493 | C | T | 2 | a0013c0014t0001g0022 a0013c0014t0001g0121 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3006-681C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783493 | |||||||
chr1:11783575 | C | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.3006-599C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783575 | |||||||
chr1:11783576 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3006-598T>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783576 | |||||||
chr1:11783617 | G | C | 5 | a0013c0014t0001g0022 a0013c0014t0001g0047 a0013c0014t0001g0118 others(2): Show |
5 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3006-557G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783617 | |||||||
chr1:11783626 | G | A | 46 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(43): Show |
47 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.3006-548G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783626 | |||||||
chr1:11783783 | G | A | 14 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.3006-391G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783783 | |||||||
chr1:11783852 | GTTTTGTT others(3): Show |
G | 14 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(11): Show |
14 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.3006-313_3006-304d others(12): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr1 | 11783852 | ||||||
chr1:11783862 | A | G | 46 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(43): Show |
47 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.3006-312A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11783862 | |||||||
chr1:11784157 | A | T | 39 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(36): Show |
45 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.3006-17A>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 14/20 | chr1 | 11784157 | |||||||
chr1:11784680 | A | G | 38 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(35): Show |
39 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.3425+87A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/20 | chr1 | 11784680 | |||||||
chr1:11784770 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(305): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3425+177A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/20 | chr1 | 11784770 | |||||||
chr1:11785056 | G | A | 308 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(305): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3426-92G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/20 | chr1 | 11785056 | |||||||
chr1:11785071 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3426-77G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/20 | chr1 | 11785071 | |||||||
chr1:11785080 | TG | T | 11 | a0009c0008t0001g0042 a0009c0008t0001g0043 a0009c0008t0001g0048 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.3426-61delG | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr1 | 11785080 | ||||||
chr1:11785110 | TTTA | T | 38 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(35): Show |
39 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.3426-36_3426-34del others(3): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr1 | 11785110 | ||||||
chr1:11785112 | T | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
191 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.3426-36T>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 15/20 | chr1 | 11785112 | |||||||
chr1:11785318 | C | T | 11 | a0009c0008t0001g0042 a0009c0008t0001g0043 a0009c0008t0001g0048 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.3567+29C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11785318 | |||||||
chr1:11785459 | C | T | 4 | a0014c0015t0001g0017 a0014c0015t0001g0115 a0014c0015t0001g0116 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3567+170C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11785459 | |||||||
chr1:11785461 | G | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.3567+172G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11785461 | |||||||
chr1:11785467 | G | A | 38 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(35): Show |
39 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.3567+178G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11785467 | |||||||
chr1:11785513 | C | T | 39 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(36): Show |
45 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.3567+224C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11785513 | |||||||
chr1:11785534 | A | C | 1 | a0013c0014t0001g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3567+245A>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11785534 | |||||||
chr1:11785618 | C | T | 1 | a0032c0047t0001g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3567+329C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11785618 | |||||||
chr1:11785889 | C | T | 29 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0079 others(26): Show |
31 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.3567+600C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11785889 | |||||||
chr1:11786001 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3567+712G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786001 | |||||||
chr1:11786035 | G | GT | 323 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.3567+757dupT | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr1 | 11786035 | ||||||
chr1:11786186 | C | T | 1 | a0001c0009t0001g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3567+897C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786186 | |||||||
chr1:11786195 | G | A | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
243 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.3567+906G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786195 | |||||||
chr1:11786213 | T | C | 6 | a0023c0025t0001g0196 a0023c0025t0001g0250 a0029c0033t0001g0291 others(3): Show |
6 | HG00438.hp1 HG02293.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.3567+924T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786213 | |||||||
chr1:11786378 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3568-1010C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786378 | |||||||
chr1:11786384 | G | T | 1 | a0001c0001t0001g0242 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3568-1004G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786384 | |||||||
chr1:11786390 | G | A | 308 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(305): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3568-998G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786390 | |||||||
chr1:11786596 | C | T | 2 | a0021c0016t0001g0197 a0021c0016t0001g0289 |
2 | NA18986.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.3568-792C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786596 | |||||||
chr1:11786602 | A | ATT | 30 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(27): Show |
36 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.3568-768_3568-767d others(4): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr1 | 11786602 | ||||||
chr1:11786602 | ATTTT | A | 179 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
190 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.3568-770_3568-767d others(6): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr1 | 11786602 | ||||||
chr1:11786602 | ATTTTTT | A | 11 | a0009c0008t0001g0042 a0009c0008t0001g0043 a0009c0008t0001g0048 others(8): Show |
11 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.3568-772_3568-767d others(8): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr1 | 11786602 | ||||||
chr1:11786602 | ATTTTTTT others(1): Show |
A | 17 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(14): Show |
17 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.3568-774_3568-767d others(10): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr1 | 11786602 | ||||||
chr1:11786685 | C | T | 38 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(35): Show |
39 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.3568-703C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786685 | |||||||
chr1:11786706 | A | G | 8 | a0012c0013t0001g0120 a0012c0013t0002g0030 a0012c0013t0002g0147 others(5): Show |
8 | HG01109.hp2 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.3568-682A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786706 | |||||||
chr1:11786707 | T | C | 3 | a0029c0033t0001g0291 a0042c0040t0001g0317 a0052c0049t0001g0230 |
3 | HG00438.hp1 HG03017.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3568-681T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786707 | |||||||
chr1:11786791 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3568-597G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11786791 | |||||||
chr1:11787037 | A | G | 2 | a0036c0032t0001g0095 a0039c0043t0002g0021 |
2 | HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3568-351A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11787037 | |||||||
chr1:11787110 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3568-278C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11787110 | |||||||
chr1:11787269 | G | A | 1 | a0037c0060t0003g0113 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3568-119G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11787269 | |||||||
chr1:11787277 | G | GGAA | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
193 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.3568-108_3568-106d others(5): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr1 | 11787277 | ||||||
chr1:11787278 | G | C | 1 | a0007c0010t0001g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3568-110G>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11787278 | |||||||
chr1:11787287 | G | A | 1 | a0029c0033t0001g0291 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3568-101G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11787287 | |||||||
chr1:11787379 | T | C | 17 | a0005c0004t0001g0064 a0005c0004t0001g0071 a0005c0004t0001g0098 others(14): Show |
17 | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.3568-9T>C | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 16/20 | chr1 | 11787379 | |||||||
chr1:11787511 | C | G | 1 | a0002c0002t0001g0179 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3673+18C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 17/20 | chr1 | 11787511 | |||||||
chr1:11787592 | G | A | 1 | a0045c0029t0001g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3673+99G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 17/20 | chr1 | 11787592 | |||||||
chr1:11787683 | CCT | C | 5 | a0023c0025t0001g0196 a0023c0025t0001g0250 a0029c0033t0001g0291 others(2): Show |
5 | HG00438.hp1 HG02293.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.3674-189_3674-188d others(4): Show |
C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 17/20 | chr1 | 11787683 | |||||||
chr1:11787702 | C | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.3674-171C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 17/20 | chr1 | 11787702 | |||||||
chr1:11787703 | G | A | 4 | a0014c0015t0001g0017 a0014c0015t0001g0115 a0014c0015t0001g0116 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3674-170G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 17/20 | chr1 | 11787703 | |||||||
chr1:11787715 | G | T | 36 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(33): Show |
37 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.3674-158G>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 17/20 | chr1 | 11787715 | |||||||
chr1:11787804 | G | A | 35 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(32): Show |
36 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.3674-69G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 17/20 | chr1 | 11787804 | |||||||
chr1:11787845 | C | A | 35 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(32): Show |
36 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.3674-28C>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 17/20 | chr1 | 11787845 | |||||||
chr1:11788082 | G | A | 43 | a0002c0002t0001g0001 a0002c0002t0001g0003 a0002c0002t0001g0007 others(40): Show |
49 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.3848+35G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 18/20 | chr1 | 11788082 | |||||||
chr1:11788127 | C | T | 2 | a0027c0022t0001g0169 a0027c0022t0001g0198 |
2 | NA18971.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.3849-22C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 18/20 | chr1 | 11788127 | |||||||
chr1:11788542 | C | A | 1 | a0004c0007t0001g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4079-110C>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 19/20 | chr1 | 11788542 | |||||||
chr1:11788613 | G | A | 2 | a0007c0010t0001g0039 a0037c0060t0003g0113 |
2 | HG02257.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.4079-39G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 19/20 | chr1 | 11788613 | |||||||
chr1:11788627 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0108 |
3 | HG01516.hp1 HG01517.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.4079-25C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 19/20 | chr1 | 11788627 | |||||||
chr1:11788822 | A | G | 307 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(304): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.4173+76A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 20/20 | chr1 | 11788822 | |||||||
chr1:11788828 | C | T | 4 | a0012c0013t0001g0120 a0012c0013t0002g0030 a0012c0013t0002g0147 others(1): Show |
4 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4173+82C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 20/20 | chr1 | 11788828 | |||||||
chr1:11788866 | C | T | 3 | a0010c0037t0001g0036 a0016c0018t0001g0028 a0016c0018t0001g0051 |
3 | HG02145.hp2 HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4173+120C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 20/20 | chr1 | 11788866 | |||||||
chr1:11788915 | G | A | 42 | a0003c0003t0001g0010 a0003c0003t0001g0075 a0003c0003t0001g0105 others(39): Show |
43 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.4173+169G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 20/20 | chr1 | 11788915 | |||||||
chr1:11789024 | A | G | 2 | a0001c0001t0001g0265 a0001c0001t0001g0267 |
2 | NA18969.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.4174-246A>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 20/20 | chr1 | 11789024 | |||||||
chr1:11789040 | C | G | 1 | a0021c0016t0001g0276 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4174-230C>G | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 20/20 | chr1 | 11789040 | |||||||
chr1:11789192 | G | A | 2 | a0013c0014t0001g0022 a0013c0014t0001g0121 |
2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4174-78G>A | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 20/20 | chr1 | 11789192 | |||||||
chr1:11789258 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0221 |
2 | NA19004.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.4174-12C>T | C1orf167 | ENSG00000215910.8 | transcript | ENST00000688073.1 | protein_coding | 20/20 | chr1 | 11789258 |