Item | Value |
---|---|
geneid | 283638 |
ensemblid | ENSG00000099814.17 |
hgncid | 20362 |
symbol | CEP170B |
name | centrosomal protein 170B |
refseq_nuc | NM_001112726.3 |
refseq_prot | NP_001106197.1 |
ensembl_nuc | ENST00000414716.8 |
ensembl_prot | ENSP00000404151.2 |
mane_status | MANE Select |
chr | chr14 |
start | 104865268 |
end | 104896747 |
strand | + |
ver | v1.2 |
region | chr14:104865268-104896747 |
region5000 | chr14:104860268-104901747 |
regionname0 | CEP170B_chr14_104865268_104896747 |
regionname5000 | CEP170B_chr14_104860268_104901747 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1554 | 251 | 70 | 61 | 73 | 10 | 35 | 52 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0002 | 0/0 | 1552 | 33 | 2 | 12 | 12 | 0 | 7 | 7 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1547): Show |
chr14 | 104860268 | 104901747 |
a0003 | 0/0 | 1554 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0004 | 0/0 | 1554 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0005 | 0/0 | 1554 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0006 | 0/0 | 1552 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1547): Show |
chr14 | 104860268 | 104901747 |
a0007 | 0/0 | 1554 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0008 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0009 | 0/0 | 1554 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0010 | 0/0 | 1554 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0011 | 0/0 | 1554 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0012 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0013 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0014 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0015 | 0/0 | 1552 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1547): Show |
chr14 | 104860268 | 104901747 |
a0016 | 0/0 | 1554 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0017 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0018 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0019 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0020 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0021 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0022 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0023 | 0/0 | 1554 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0024 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0025 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1555): Show |
chr14 | 104860268 | 104901747 |
a0026 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0027 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0028 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0029 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0030 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0031 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
a0032 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | MSATS others(1549): Show |
chr14 | 104860268 | 104901747 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 4662 | 104 | 16 | 18 | 55 | 4 | 10 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0002 | 0/0 | 4662 | 25 | 0 | 14 | 3 | 2 | 6 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0003 | 0/0 | 4662 | 22 | 3 | 11 | 0 | 1 | 7 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0005 | 0/0 | 4662 | 10 | 9 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0006 | 0/0 | 4662 | 8 | 0 | 2 | 1 | 0 | 5 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0007 | 0/0 | 4662 | 8 | 8 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0008 | 0/0 | 4662 | 8 | 7 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0010 | 0/0 | 4662 | 6 | 0 | 2 | 0 | 2 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0011 | 0/0 | 4662 | 5 | 0 | 1 | 4 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0013 | 0/1 | 4662 | 3 | 0 | 0 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0014 | 0/0 | 4662 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0015 | 0/0 | 4662 | 3 | 1 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0017 | 0/0 | 4662 | 3 | 0 | 2 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0018 | 0/0 | 4662 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0019 | 0/0 | 4662 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0020 | 0/0 | 4662 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0022 | 0/0 | 4662 | 3 | 0 | 1 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0023 | 0/0 | 4662 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0032 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0034 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0035 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0037 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0038 | 0/0 | 4662 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0041 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0042 | 0/0 | 4662 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0048 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0053 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0054 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0055 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0058 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0059 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0061 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0062 | 0/0 | 4662 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0065 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0066 | 0/0 | 4662 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0069 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0070 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0071 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0073 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0074 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0075 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0077 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0080 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0082 | 0/0 | 4662 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0083 | 0/0 | 4662 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0087 | 0/0 | 4662 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0001c0088 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0002c0004 | 0/0 | 4656 | 16 | 1 | 4 | 9 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4651): Show |
chr14 | 104860268 | 104901747 | ||
a0002c0009 | 0/0 | 4656 | 7 | 0 | 7 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4651): Show |
chr14 | 104860268 | 104901747 | ||
a0002c0012 | 0/0 | 4656 | 4 | 0 | 0 | 0 | 0 | 4 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4651): Show |
chr14 | 104860268 | 104901747 | ||
a0002c0028 | 0/0 | 4656 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4651): Show |
chr14 | 104860268 | 104901747 | ||
a0002c0029 | 0/0 | 4656 | 2 | 1 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4651): Show |
chr14 | 104860268 | 104901747 | ||
a0002c0060 | 0/0 | 4656 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4651): Show |
chr14 | 104860268 | 104901747 | ||
a0002c0064 | 0/0 | 4656 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4651): Show |
chr14 | 104860268 | 104901747 | ||
a0003c0026 | 0/0 | 4662 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0003c0067 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0003c0078 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0004c0021 | 0/0 | 4662 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0004c0081 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0005c0016 | 0/0 | 4662 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0006c0030 | 0/0 | 4656 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4651): Show |
chr14 | 104860268 | 104901747 | ||
a0007c0024 | 0/0 | 4662 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0008c0027 | 0/0 | 4662 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0009c0025 | 0/0 | 4662 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0010c0063 | 0/0 | 4662 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0010c0086 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0011c0046 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0011c0047 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0012c0036 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0013c0039 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0014c0045 | 0/0 | 4662 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0015c0089 | 0/0 | 4656 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4651): Show |
chr14 | 104860268 | 104901747 | ||
a0016c0084 | 0/0 | 4662 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0017c0043 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0018c0079 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0019c0056 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0020c0040 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0021c0052 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0022c0068 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0023c0049 | 0/0 | 4662 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0024c0050 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0025c0085 | 0/0 | 4680 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4675): Show |
chr14 | 104860268 | 104901747 | ||
a0026c0076 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0027c0044 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0028c0031 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0029c0033 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0030c0057 | 0/0 | 4662 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0031c0051 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 | ||
a0032c0072 | 0/0 | 4662 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | ATGAG others(4657): Show |
chr14 | 104860268 | 104901747 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6727 | 81 | 14 | 16 | 38 | 3 | 9 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0001t0002 | 0/0 | 6727 | 3 | 0 | 0 | 2 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0001t0004 | 0/0 | 6727 | 13 | 0 | 2 | 11 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0001t0010 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0001t0015 | 0/0 | 6727 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0001t0016 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0001t0023 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0001t0025 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0001t0026 | 0/0 | 6731 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6726): Show |
chr14 | 104860268 | 104901747 |
a0001c0001t0027 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0002t0002 | 0/0 | 6727 | 25 | 0 | 14 | 3 | 2 | 6 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0003t0002 | 0/0 | 6727 | 20 | 3 | 11 | 0 | 0 | 6 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0003t0021 | 0/0 | 6727 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0003t0022 | 0/0 | 6727 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0005t0003 | 0/0 | 6731 | 10 | 9 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6726): Show |
chr14 | 104860268 | 104901747 |
a0001c0006t0005 | 0/0 | 6727 | 6 | 0 | 1 | 0 | 0 | 5 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0006t0007 | 0/0 | 6727 | 2 | 0 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0007t0001 | 0/0 | 6727 | 5 | 5 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0007t0008 | 0/0 | 6727 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0008t0003 | 0/0 | 6731 | 8 | 7 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6726): Show |
chr14 | 104860268 | 104901747 |
a0001c0010t0002 | 0/0 | 6727 | 6 | 0 | 2 | 0 | 2 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0011t0001 | 0/0 | 6727 | 5 | 0 | 1 | 4 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0013t0002 | 0/0 | 6727 | 2 | 0 | 0 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0013t0019 | 0/1 | 6728 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6723): Show |
chr14 | 104860268 | 104901747 |
a0001c0014t0001 | 0/0 | 6727 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0015t0001 | 0/0 | 6727 | 3 | 1 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0017t0002 | 0/0 | 6727 | 3 | 0 | 2 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0018t0003 | 0/0 | 6731 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6726): Show |
chr14 | 104860268 | 104901747 |
a0001c0019t0002 | 0/0 | 6727 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0020t0002 | 0/0 | 6727 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0022t0001 | 0/0 | 6727 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0022t0004 | 0/0 | 6727 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0023t0004 | 0/0 | 6727 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0032t0024 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0034t0004 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0035t0013 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0037t0005 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0038t0005 | 0/0 | 6727 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0041t0001 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0042t0001 | 0/0 | 6727 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0048t0001 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0053t0001 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0054t0001 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0055t0001 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0058t0001 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0059t0001 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0061t0017 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0062t0002 | 0/0 | 6727 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0065t0002 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0066t0001 | 0/0 | 6727 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0069t0002 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0070t0001 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0071t0003 | 0/0 | 6731 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6726): Show |
chr14 | 104860268 | 104901747 |
a0001c0073t0002 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0074t0002 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0075t0002 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0077t0001 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0080t0018 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0082t0002 | 0/0 | 6727 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0083t0002 | 0/0 | 6727 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0087t0002 | 0/0 | 6727 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0001c0088t0002 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0002c0004t0002 | 0/0 | 6721 | 16 | 1 | 4 | 9 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6716): Show |
chr14 | 104860268 | 104901747 |
a0002c0009t0002 | 0/0 | 6721 | 6 | 0 | 6 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6716): Show |
chr14 | 104860268 | 104901747 |
a0002c0009t0012 | 0/0 | 6721 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6716): Show |
chr14 | 104860268 | 104901747 |
a0002c0012t0002 | 0/0 | 6721 | 4 | 0 | 0 | 0 | 0 | 4 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6716): Show |
chr14 | 104860268 | 104901747 |
a0002c0028t0002 | 0/0 | 6721 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6716): Show |
chr14 | 104860268 | 104901747 |
a0002c0029t0002 | 0/0 | 6721 | 2 | 1 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6716): Show |
chr14 | 104860268 | 104901747 |
a0002c0060t0002 | 0/0 | 6721 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6716): Show |
chr14 | 104860268 | 104901747 |
a0002c0064t0002 | 0/0 | 6721 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6716): Show |
chr14 | 104860268 | 104901747 |
a0003c0026t0002 | 0/0 | 6727 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0003c0067t0002 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0003c0078t0002 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0004c0021t0006 | 0/0 | 6727 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0004c0081t0006 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0005c0016t0001 | 0/0 | 6727 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0005c0016t0014 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0006c0030t0002 | 0/0 | 6721 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6716): Show |
chr14 | 104860268 | 104901747 |
a0007c0024t0001 | 0/0 | 6727 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0008c0027t0003 | 0/0 | 6731 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6726): Show |
chr14 | 104860268 | 104901747 |
a0009c0025t0002 | 0/0 | 6727 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0010c0063t0002 | 0/0 | 6727 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0010c0086t0002 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0011c0046t0004 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0011c0047t0004 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0012c0036t0007 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0013c0039t0001 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0014c0045t0001 | 0/0 | 6727 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0015c0089t0002 | 0/0 | 6721 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6716): Show |
chr14 | 104860268 | 104901747 |
a0016c0084t0002 | 0/0 | 6727 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0017c0043t0001 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0018c0079t0001 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0019c0056t0001 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0020c0040t0011 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0021c0052t0001 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0022c0068t0020 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0023c0049t0001 | 0/0 | 6727 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0024c0050t0001 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0025c0085t0002 | 0/0 | 6745 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6740): Show |
chr14 | 104860268 | 104901747 |
a0026c0076t0004 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0027c0044t0001 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0028c0031t0001 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0029c0033t0009 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACA others(6722): Show |
chr14 | 104860268 | 104901747 |
a0030c0057t0001 | 0/0 | 6727 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0031c0051t0001 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
a0032c0072t0002 | 0/0 | 6727 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | AGACG others(6722): Show |
chr14 | 104860268 | 104901747 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0010g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0015g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0023g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0025g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0026g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0001t0027g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0004 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0003 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0021g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0003t0022g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0005t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0005g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0006t0007g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0007t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0008t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0010t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0010t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0010t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0010t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0010t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0011t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0011t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0011t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0011t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0011t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0013t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0013t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0013t0019g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0014t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0014t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0015t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0015t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0015t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0017t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0017t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0017t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0018t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0019t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0019t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0019t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0020t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0020t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0020t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0022t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0022t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0022t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0023t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0032t0024g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0034t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0035t0013g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0037t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0038t0005g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0041t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0042t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0048t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0053t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0054t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0055t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0058t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0059t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0061t0017g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0062t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0065t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0066t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0069t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0070t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0071t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0073t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0074t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0075t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0077t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0080t0018g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0082t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0083t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0087t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0001c0088t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0004t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0009t0002g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0009t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0009t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0009t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0009t0012g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0012t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0012t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0012t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0028t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0028t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0029t0002g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0060t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0002c0064t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0003c0026t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0003c0026t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0003c0067t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0003c0078t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0004c0021t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0004c0021t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0004c0021t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0004c0081t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0005c0016t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0005c0016t0014g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0006c0030t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0006c0030t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0007c0024t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0007c0024t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0008c0027t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0008c0027t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0009c0025t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0010c0063t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0010c0086t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0011c0046t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0011c0047t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0012c0036t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0013c0039t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0014c0045t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0015c0089t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0016c0084t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0017c0043t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0018c0079t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0019c0056t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0020c0040t0011g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0021c0052t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0022c0068t0020g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0023c0049t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0024c0050t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0025c0085t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0026c0076t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0027c0044t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0028c0031t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0029c0033t0009g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0030c0057t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0031c0051t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
a0032c0072t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0221 | EUR | GBR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00280 | hp1 | a0001 | c0010 | t0002 | g0060 | EUR | FIN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00280 | hp2 | a0001 | c0003 | t0021 | g0231 | EUR | FIN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00408 | hp2 | a0006 | c0030 | t0002 | g0196 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00438 | hp1 | a0012 | c0036 | t0007 | g0151 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00438 | hp2 | a0007 | c0024 | t0001 | g0094 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00544 | hp1 | a0002 | c0004 | t0002 | g0036 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00621 | hp1 | a0013 | c0039 | t0001 | g0102 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00733 | hp1 | a0014 | c0045 | t0001 | g0137 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00733 | hp2 | a0001 | c0019 | t0002 | g0159 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0210 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01069 | hp2 | a0001 | c0017 | t0002 | g0166 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01071 | hp1 | a0002 | c0004 | t0002 | g0189 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01071 | hp2 | a0001 | c0017 | t0002 | g0165 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0174 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01074 | hp2 | a0015 | c0089 | t0002 | g0009 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01081 | hp1 | a0001 | c0003 | t0002 | g0190 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01099 | hp1 | a0001 | c0006 | t0005 | g0043 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01099 | hp2 | a0001 | c0083 | t0002 | g0212 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01106 | hp1 | a0001 | c0003 | t0002 | g0181 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01106 | hp2 | a0002 | c0004 | t0002 | g0171 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0207 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01109 | hp2 | a0001 | c0003 | t0002 | g0218 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01167 | hp2 | a0001 | c0008 | t0003 | g0247 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01168 | hp2 | a0002 | c0009 | t0012 | g0175 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01175 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01192 | hp1 | a0001 | c0003 | t0002 | g0227 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01255 | hp1 | a0001 | c0005 | t0003 | g0238 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01255 | hp2 | a0001 | c0010 | t0002 | g0058 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01256 | hp1 | a0002 | c0009 | t0002 | g0009 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01257 | hp1 | a0016 | c0084 | t0002 | g0223 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01257 | hp2 | a0002 | c0004 | t0002 | g0035 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01258 | hp1 | a0002 | c0004 | t0002 | g0035 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01261 | hp1 | a0001 | c0066 | t0001 | g0114 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01261 | hp2 | a0001 | c0087 | t0002 | g0195 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01346 | hp1 | a0001 | c0015 | t0001 | g0066 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01358 | hp2 | a0001 | c0003 | t0002 | g0208 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01361 | hp1 | a0001 | c0011 | t0001 | g0126 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01361 | hp2 | a0002 | c0029 | t0002 | g0037 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01496 | hp1 | a0001 | c0006 | t0007 | g0029 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01496 | hp2 | a0001 | c0062 | t0002 | g0169 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01516 | hp1 | a0001 | c0017 | t0002 | g0162 | EUR | IBS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01884 | hp1 | a0003 | c0026 | t0002 | g0237 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01884 | hp2 | a0001 | c0080 | t0018 | g0080 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01891 | hp1 | a0001 | c0070 | t0001 | g0158 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01891 | hp2 | a0001 | c0007 | t0001 | g0019 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01928 | hp1 | a0001 | c0003 | t0002 | g0222 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01928 | hp2 | a0001 | c0003 | t0002 | g0229 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01934 | hp1 | a0001 | c0019 | t0002 | g0160 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01934 | hp2 | a0002 | c0009 | t0002 | g0009 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0182 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01975 | hp2 | a0001 | c0010 | t0002 | g0059 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01978 | hp2 | a0001 | c0003 | t0002 | g0228 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01981 | hp1 | a0002 | c0009 | t0002 | g0219 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01993 | hp1 | a0002 | c0009 | t0002 | g0009 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02004 | hp1 | a0002 | c0009 | t0002 | g0193 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02004 | hp2 | a0001 | c0022 | t0001 | g0225 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02015 | hp2 | a0001 | c0001 | t0025 | g0017 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02027 | hp1 | a0017 | c0043 | t0001 | g0098 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02027 | hp2 | a0002 | c0004 | t0002 | g0002 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02055 | hp1 | a0008 | c0027 | t0003 | g0249 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02055 | hp2 | a0001 | c0007 | t0008 | g0130 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02080 | hp1 | a0001 | c0011 | t0001 | g0117 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02132 | hp2 | a0002 | c0004 | t0002 | g0002 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02135 | hp2 | a0002 | c0004 | t0002 | g0002 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02145 | hp1 | a0002 | c0004 | t0002 | g0173 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02148 | hp1 | a0002 | c0009 | t0002 | g0201 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | CDX | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02257 | hp1 | a0002 | c0029 | t0002 | g0037 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02257 | hp2 | a0001 | c0020 | t0002 | g0031 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02258 | hp1 | a0001 | c0005 | t0003 | g0246 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02258 | hp2 | a0001 | c0005 | t0003 | g0242 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02280 | hp2 | a0001 | c0018 | t0003 | g0014 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0215 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02293 | hp2 | a0001 | c0003 | t0002 | g0226 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02451 | hp1 | a0001 | c0020 | t0002 | g0156 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02451 | hp2 | a0001 | c0059 | t0001 | g0078 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02523 | hp2 | a0002 | c0004 | t0002 | g0203 | EAS | KHV | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02572 | hp1 | a0005 | c0016 | t0001 | g0025 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02572 | hp2 | a0001 | c0005 | t0003 | g0240 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02615 | hp1 | a0019 | c0056 | t0001 | g0097 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02615 | hp2 | a0001 | c0005 | t0003 | g0038 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02622 | hp1 | a0001 | c0053 | t0001 | g0085 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02622 | hp2 | a0004 | c0021 | t0006 | g0232 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02630 | hp1 | a0001 | c0007 | t0001 | g0136 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02630 | hp2 | a0001 | c0005 | t0003 | g0241 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02647 | hp1 | a0001 | c0075 | t0002 | g0154 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02647 | hp2 | a0001 | c0005 | t0003 | g0038 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02683 | hp2 | a0001 | c0003 | t0022 | g0187 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02698 | hp1 | a0001 | c0082 | t0002 | g0033 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02698 | hp2 | a0001 | c0006 | t0005 | g0028 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02717 | hp1 | a0001 | c0003 | t0002 | g0211 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02717 | hp2 | a0003 | c0078 | t0002 | g0236 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02723 | hp1 | a0020 | c0040 | t0011 | g0258 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02723 | hp2 | a0001 | c0071 | t0003 | g0239 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02735 | hp1 | a0002 | c0012 | t0002 | g0197 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02735 | hp2 | a0001 | c0006 | t0005 | g0146 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02738 | hp2 | a0001 | c0003 | t0002 | g0178 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02809 | hp1 | a0001 | c0073 | t0002 | g0155 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02809 | hp2 | a0021 | c0052 | t0001 | g0055 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02818 | hp1 | a0001 | c0008 | t0003 | g0248 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02818 | hp2 | a0001 | c0020 | t0002 | g0152 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02896 | hp1 | a0001 | c0008 | t0003 | g0015 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02897 | hp2 | a0001 | c0008 | t0003 | g0015 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02922 | hp1 | a0001 | c0077 | t0001 | g0087 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02922 | hp2 | a0001 | c0054 | t0001 | g0081 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02965 | hp1 | a0001 | c0007 | t0008 | g0131 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02965 | hp2 | a0001 | c0018 | t0003 | g0014 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02970 | hp1 | a0001 | c0005 | t0003 | g0244 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02976 | hp1 | a0003 | c0067 | t0002 | g0030 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02976 | hp2 | a0001 | c0015 | t0001 | g0104 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03017 | hp2 | a0001 | c0003 | t0002 | g0180 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03041 | hp1 | a0022 | c0068 | t0020 | g0082 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03041 | hp2 | a0001 | c0005 | t0003 | g0243 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03098 | hp1 | a0001 | c0001 | t0026 | g0251 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03098 | hp2 | a0001 | c0008 | t0003 | g0253 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03130 | hp1 | a0001 | c0048 | t0001 | g0123 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03130 | hp2 | a0001 | c0001 | t0023 | g0090 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03139 | hp1 | a0001 | c0014 | t0001 | g0018 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03139 | hp2 | a0001 | c0007 | t0008 | g0134 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03195 | hp1 | a0001 | c0018 | t0003 | g0014 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03195 | hp2 | a0001 | c0065 | t0002 | g0255 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03225 | hp2 | a0001 | c0008 | t0003 | g0245 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03239 | hp2 | a0001 | c0010 | t0002 | g0010 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03453 | hp1 | a0001 | c0032 | t0024 | g0167 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03453 | hp2 | a0009 | c0025 | t0002 | g0039 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03486 | hp1 | a0001 | c0008 | t0003 | g0252 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03486 | hp2 | a0001 | c0007 | t0001 | g0111 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03490 | hp1 | a0001 | c0013 | t0002 | g0044 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03490 | hp2 | a0002 | c0012 | t0002 | g0002 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0034 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0034 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03492 | hp2 | a0002 | c0012 | t0002 | g0002 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03540 | hp2 | a0001 | c0003 | t0002 | g0003 | AFR | GWD | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03579 | hp1 | a0005 | c0016 | t0001 | g0025 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03579 | hp2 | a0005 | c0016 | t0014 | g0088 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03654 | hp1 | a0010 | c0063 | t0002 | g0161 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03654 | hp2 | a0001 | c0006 | t0005 | g0256 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0172 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03669 | hp2 | a0002 | c0004 | t0002 | g0213 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0033 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03704 | hp1 | a0001 | c0010 | t0002 | g0056 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03710 | hp1 | a0001 | c0038 | t0005 | g0168 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03710 | hp2 | a0001 | c0001 | t0015 | g0048 | SAS | PJL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03831 | hp1 | a0001 | c0003 | t0002 | g0179 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03834 | hp1 | a0001 | c0042 | t0001 | g0100 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03834 | hp2 | a0001 | c0006 | t0005 | g0147 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0032 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04184 | hp1 | a0001 | c0013 | t0002 | g0010 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04199 | hp2 | a0002 | c0064 | t0002 | g0163 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04204 | hp1 | a0002 | c0004 | t0002 | g0036 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04204 | hp2 | a0023 | c0049 | t0001 | g0135 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04228 | hp1 | a0001 | c0006 | t0005 | g0076 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG04228 | hp2 | a0001 | c0003 | t0002 | g0186 | SAS | STU | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18522 | hp1 | a0004 | c0081 | t0006 | g0233 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18522 | hp2 | a0008 | c0027 | t0003 | g0250 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18747 | hp1 | a0006 | c0030 | t0002 | g0176 | EAS | CHB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18906 | hp1 | a0001 | c0005 | t0003 | g0015 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18906 | hp2 | a0001 | c0014 | t0001 | g0018 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18940 | hp2 | a0002 | c0004 | t0002 | g0198 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18944 | hp2 | a0001 | c0022 | t0004 | g0200 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18947 | hp2 | a0001 | c0015 | t0001 | g0026 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18948 | hp1 | a0001 | c0011 | t0001 | g0101 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18948 | hp2 | a0002 | c0060 | t0002 | g0177 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18960 | hp1 | a0001 | c0001 | t0010 | g0023 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18960 | hp2 | a0025 | c0085 | t0002 | g0209 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18963 | hp2 | a0001 | c0034 | t0004 | g0148 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18964 | hp1 | a0026 | c0076 | t0004 | g0063 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18969 | hp1 | a0011 | c0047 | t0004 | g0005 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18969 | hp2 | a0001 | c0055 | t0001 | g0084 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18975 | hp2 | a0002 | c0004 | t0002 | g0202 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18979 | hp2 | a0001 | c0022 | t0004 | g0199 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18982 | hp2 | a0001 | c0037 | t0005 | g0149 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18983 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18995 | hp2 | a0010 | c0086 | t0002 | g0206 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18998 | hp2 | a0007 | c0024 | t0001 | g0093 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19000 | hp2 | a0001 | c0011 | t0001 | g0075 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19002 | hp1 | a0011 | c0046 | t0004 | g0001 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19002 | hp2 | a0002 | c0004 | t0002 | g0002 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19007 | hp2 | a0001 | c0023 | t0004 | g0011 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19011 | hp2 | a0027 | c0044 | t0001 | g0122 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19030 | hp1 | a0001 | c0058 | t0001 | g0077 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19043 | hp1 | a0001 | c0088 | t0002 | g0224 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19043 | hp2 | a0001 | c0061 | t0017 | g0170 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19054 | hp1 | a0001 | c0041 | t0001 | g0145 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19055 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19057 | hp1 | a0001 | c0011 | t0001 | g0074 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19058 | hp1 | a0028 | c0031 | t0001 | g0099 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19058 | hp2 | a0029 | c0033 | t0009 | g0028 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19064 | hp2 | a0001 | c0035 | t0013 | g0150 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19067 | hp1 | a0030 | c0057 | t0001 | g0006 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19074 | hp2 | a0002 | c0028 | t0002 | g0204 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19083 | hp1 | a0002 | c0028 | t0002 | g0192 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19087 | hp1 | a0001 | c0023 | t0004 | g0011 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19088 | hp1 | a0001 | c0001 | t0027 | g0125 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19089 | hp1 | a0002 | c0004 | t0002 | g0194 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19089 | hp2 | a0001 | c0006 | t0007 | g0029 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19240 | hp1 | a0001 | c0007 | t0001 | g0019 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA19240 | hp2 | a0001 | c0069 | t0002 | g0031 | AFR | YRI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20129 | hp1 | a0001 | c0074 | t0002 | g0153 | AFR | ASW | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20129 | hp2 | a0031 | c0051 | t0001 | g0120 | AFR | ASW | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20752 | hp1 | a0001 | c0010 | t0002 | g0010 | EUR | TSI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0230 | EUR | TSI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0217 | EUR | TSI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20905 | hp1 | a0002 | c0012 | t0002 | g0214 | SAS | GIH | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20905 | hp2 | a0001 | c0003 | t0002 | g0188 | SAS | GIH | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG01123 | hp2 | a0001 | c0019 | t0002 | g0164 | AMR | CLM | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02109 | hp1 | a0018 | c0079 | t0001 | g0040 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02109 | hp2 | a0001 | c0014 | t0001 | g0079 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02486 | hp1 | a0001 | c0007 | t0001 | g0129 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02559 | hp1 | a0004 | c0021 | t0006 | g0234 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG03471 | hp2 | a0001 | c0008 | t0003 | g0254 | AFR | MSL | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG06807 | hp1 | a0004 | c0021 | t0006 | g0235 | AFR | USA | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
HG06807 | hp2 | a0009 | c0025 | t0002 | g0039 | AFR | USA | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA18955 | hp2 | a0024 | c0050 | t0001 | g0073 | EAS | JPT | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20300 | hp1 | a0003 | c0026 | t0002 | g0030 | AFR | USA | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | USA | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA21309 | hp1 | a0001 | c0003 | t0002 | g0183 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
NA21309 | hp2 | a0032 | c0072 | t0002 | g0157 | AFR | LWK | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
homoSapiens | chm13v2 | a0001 | c0013 | t0019 | g0053 | REF | REF | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0119 | REF | REF | CEP170B_chr14_104860268_104901747 | CEP170B | chr14 | 104860268 | 104901747 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104868494 | G | C | 1 | a0028 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.44G>C | p.Arg15Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/19 | 317/6727 | 44/4665 | 15/1554 | chr14 | 104868494 | |||
chr14:104880396 | C | T | 1 | a0015 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.443C>T | p.Pro148Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/19 | 716/6727 | 443/4665 | 148/1554 | chr14 | 104880396 | |||
chr14:104883164 | C | T | 1 | a0003 | 4 | HG01884.hp1 HG02717.hp2 HG02976.hp1 others(1): Show |
missense_variant | MODERATE | c.707C>T | p.Pro236Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 980/6727 | 707/4665 | 236/1554 | chr14 | 104883164 | |||
chr14:104883167 | C | T | 1 | a0006 | 2 | HG00408.hp2 NA18747.hp1 |
missense_variant | MODERATE | c.710C>T | p.Ser237Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 983/6727 | 710/4665 | 237/1554 | chr14 | 104883167 | |||
chr14:104883233 | C | T | 1 | a0005 | 3 | HG02572.hp1 HG03579.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.776C>T | p.Ala259Val | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1049/6727 | 776/4665 | 259/1554 | chr14 | 104883233 | |||
chr14:104883350 | C | T | 1 | a0030 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.893C>T | p.Pro298Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1166/6727 | 893/4665 | 298/1554 | chr14 | 104883350 | |||
chr14:104883362 | C | T | 1 | a0019 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.905C>T | p.Ala302Val | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1178/6727 | 905/4665 | 302/1554 | chr14 | 104883362 | |||
chr14:104883417 | G | C | 1 | a0013 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.960G>C | p.Gln320His | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1233/6727 | 960/4665 | 320/1554 | chr14 | 104883417 | |||
chr14:104883460 | C | T | 1 | a0026 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.1003C>T | p.Arg335Cys | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1276/6727 | 1003/4665 | 335/1554 | chr14 | 104883460 | |||
chr14:104883885 | C | T | 1 | a0031 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1106C>T | p.Ala369Val | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1379/6727 | 1106/4665 | 369/1554 | chr14 | 104883885 | |||
chr14:104884143 | G | A | 1 | a0029 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.1364G>A | p.Gly455Glu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1637/6727 | 1364/4665 | 455/1554 | chr14 | 104884143 | |||
chr14:104884218 | C | T | 1 | a0022 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1439C>T | p.Ser480Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1712/6727 | 1439/4665 | 480/1554 | chr14 | 104884218 | |||
chr14:104884314 | C | T | 1 | a0011 | 2 | NA18969.hp1 NA19002.hp1 |
missense_variant | MODERATE | c.1535C>T | p.Ser512Phe | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1808/6727 | 1535/4665 | 512/1554 | chr14 | 104884314 | |||
chr14:104884322 | G | A | 1 | a0020 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1543G>A | p.Ala515Thr | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1816/6727 | 1543/4665 | 515/1554 | chr14 | 104884322 | |||
chr14:104884410 | C | A | 1 | a0021 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1631C>A | p.Pro544Gln | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1904/6727 | 1631/4665 | 544/1554 | chr14 | 104884410 | |||
chr14:104885484 | C | T | 1 | a0014 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.1886C>T | p.Ala629Val | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/19 | 2159/6727 | 1886/4665 | 629/1554 | chr14 | 104885484 | |||
chr14:104886305 | C | T | 1 | a0027 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.2066C>T | p.Pro689Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2339/6727 | 2066/4665 | 689/1554 | chr14 | 104886305 | |||
chr14:104886314 | C | T | 1 | a0016 | 1 | HG01257.hp1 | missense_variant | MODERATE | c.2075C>T | p.Ser692Phe | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2348/6727 | 2075/4665 | 692/1554 | chr14 | 104886314 | |||
chr14:104886547 | CGCAGGA | C | 3 | a0002 a0006 a0015 |
36 | HG00408.hp2 HG00544.hp1 HG01071.hp1 others(33): Show |
conservative_inframe_deletion | MODERATE | c.2311_2316delAGGAGC | p.Arg771_Ser772del | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2584/6727 | 2311/4665 | 771/1554 | INFO_REALIGN_3_PRIME | chr14 | 104886547 | ||
chr14:104886580 | A | T | 1 | a0024 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.2341A>T | p.Arg781Trp | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2614/6727 | 2341/4665 | 781/1554 | chr14 | 104886580 | |||
chr14:104886607 | G | A | 1 | a0008 | 2 | HG02055.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.2368G>A | p.Gly790Arg | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2641/6727 | 2368/4665 | 790/1554 | chr14 | 104886607 | |||
chr14:104886674 | C | T | 2 | a0010 a0025 |
3 | HG03654.hp1 NA18960.hp2 NA18995.hp2 |
missense_variant | MODERATE | c.2435C>T | p.Pro812Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2708/6727 | 2435/4665 | 812/1554 | chr14 | 104886674 | |||
chr14:104886715 | G | A | 1 | a0032 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2476G>A | p.Ala826Thr | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2749/6727 | 2476/4665 | 826/1554 | chr14 | 104886715 | |||
chr14:104886799 | C | G | 2 | a0014 a0018 |
2 | HG00733.hp1 HG02109.hp1 |
missense_variant | MODERATE | c.2560C>G | p.Pro854Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2833/6727 | 2560/4665 | 854/1554 | chr14 | 104886799 | |||
chr14:104886811 | G | A | 1 | a0009 | 2 | HG03453.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.2572G>A | p.Gly858Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2845/6727 | 2572/4665 | 858/1554 | chr14 | 104886811 | |||
chr14:104887123 | G | A | 1 | a0007 | 2 | HG00438.hp2 NA18998.hp2 |
missense_variant | MODERATE | c.2884G>A | p.Val962Ile | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3157/6727 | 2884/4665 | 962/1554 | chr14 | 104887123 | |||
chr14:104887141 | A | C | 1 | a0030 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.2902A>C | p.Lys968Gln | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3175/6727 | 2902/4665 | 968/1554 | chr14 | 104887141 | |||
chr14:104887366 | T | C | 1 | a0023 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.3127T>C | p.Trp1043Arg | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3400/6727 | 3127/4665 | 1043/1554 | chr14 | 104887366 | |||
chr14:104887381 | C | T | 2 | a0004 a0022 |
5 | HG02559.hp1 HG02622.hp2 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.3142C>T | p.Arg1048Cys | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3415/6727 | 3142/4665 | 1048/1554 | chr14 | 104887381 | |||
chr14:104887449 | C | CACCGGGG others(11): Show |
1 | a0025 | 1 | NA18960.hp2 | conservative_inframe_insertion | MODERATE | c.3211_3228dupACCGGG others(12): Show |
p.Thr1071_Leu1076dup | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3502/6727 | 3229/4665 | 1077/1554 | INFO_REALIGN_3_PRIME | chr14 | 104887449 | ||
chr14:104887589 | C | T | 1 | a0004 | 4 | HG02559.hp1 HG02622.hp2 HG06807.hp1 others(1): Show |
missense_variant | MODERATE | c.3350C>T | p.Thr1117Ile | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3623/6727 | 3350/4665 | 1117/1554 | chr14 | 104887589 | |||
chr14:104887621 | C | T | 1 | a0017 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.3382C>T | p.Arg1128Trp | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3655/6727 | 3382/4665 | 1128/1554 | chr14 | 104887621 | |||
chr14:104889696 | T | G | 1 | a0020 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.3816T>G | p.Asp1272Glu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/19 | 4089/6727 | 3816/4665 | 1272/1554 | chr14 | 104889696 | |||
chr14:104893104 | C | T | 1 | a0012 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.4007C>T | p.Thr1336Ile | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/19 | 4280/6727 | 4007/4665 | 1336/1554 | chr14 | 104893104 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104877887 | G | A | 1 | a0001c0032 | 1 | HG03453.hp1 | splice_region_variant&synonymous_variant | LOW | c.198G>A | p.Thr66Thr | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/19 | 471/6727 | 198/4665 | 66/1554 | chr14 | 104877887 | |||
chr14:104877956 | C | T | 21 | a0001c0002 a0001c0003 a0001c0022 others(18): Show |
97 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(94): Show |
synonymous_variant | LOW | c.267C>T | p.Phe89Phe | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/19 | 540/6727 | 267/4665 | 89/1554 | chr14 | 104877956 | |||
chr14:104878460 | C | T | 1 | a0003c0078 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.292C>T | p.Leu98Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/19 | 565/6727 | 292/4665 | 98/1554 | chr14 | 104878460 | |||
chr14:104878486 | G | A | 7 | a0001c0006 a0001c0034 a0001c0035 others(4): Show |
14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
synonymous_variant | LOW | c.318G>A | p.Pro106Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/19 | 591/6727 | 318/4665 | 106/1554 | chr14 | 104878486 | |||
chr14:104880295 | G | A | 7 | a0001c0006 a0001c0034 a0001c0035 others(4): Show |
14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
synonymous_variant | LOW | c.342G>A | p.Lys114Lys | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/19 | 615/6727 | 342/4665 | 114/1554 | chr14 | 104880295 | |||
chr14:104880392 | A | C | 1 | a0001c0077 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.439A>C | p.Arg147Arg | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/19 | 712/6727 | 439/4665 | 147/1554 | chr14 | 104880392 | |||
chr14:104882783 | C | T | 1 | a0026c0076 | 1 | NA18964.hp1 | synonymous_variant | LOW | c.528C>T | p.Asp176Asp | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 7/19 | 801/6727 | 528/4665 | 176/1554 | chr14 | 104882783 | |||
chr14:104883051 | A | C | 50 | a0001c0002 a0001c0003 a0001c0005 others(47): Show |
156 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(153): Show |
synonymous_variant | LOW | c.594A>C | p.Pro198Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 867/6727 | 594/4665 | 198/1554 | chr14 | 104883051 | |||
chr14:104883111 | G | A | 1 | a0001c0082 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.654G>A | p.Ser218Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 927/6727 | 654/4665 | 218/1554 | chr14 | 104883111 | |||
chr14:104883135 | C | T | 12 | a0001c0005 a0001c0008 a0001c0020 others(9): Show |
31 | HG01167.hp2 HG01255.hp1 HG01891.hp1 others(28): Show |
synonymous_variant | LOW | c.678C>T | p.Phe226Phe | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 951/6727 | 678/4665 | 226/1554 | chr14 | 104883135 | |||
chr14:104883270 | C | T | 2 | a0001c0058 a0001c0059 |
2 | HG02451.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.813C>T | p.Ile271Ile | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1086/6727 | 813/4665 | 271/1554 | chr14 | 104883270 | |||
chr14:104883426 | G | A | 2 | a0002c0028 a0002c0060 |
3 | NA18948.hp2 NA19074.hp2 NA19083.hp1 |
synonymous_variant | LOW | c.969G>A | p.Pro323Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1242/6727 | 969/4665 | 323/1554 | chr14 | 104883426 | |||
chr14:104883471 | C | T | 1 | a0001c0055 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.1014C>T | p.Thr338Thr | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/19 | 1287/6727 | 1014/4665 | 338/1554 | chr14 | 104883471 | |||
chr14:104883841 | C | T | 16 | a0001c0003 a0001c0008 a0001c0010 others(13): Show |
57 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(54): Show |
synonymous_variant | LOW | c.1062C>T | p.His354His | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1335/6727 | 1062/4665 | 354/1554 | chr14 | 104883841 | |||
chr14:104883898 | T | C | 21 | a0001c0007 a0001c0014 a0001c0017 others(18): Show |
44 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(41): Show |
synonymous_variant | LOW | c.1119T>C | p.Ala373Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1392/6727 | 1119/4665 | 373/1554 | chr14 | 104883898 | |||
chr14:104884018 | A | G | 42 | a0001c0002 a0001c0003 a0001c0010 others(39): Show |
126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
synonymous_variant | LOW | c.1239A>G | p.Thr413Thr | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1512/6727 | 1239/4665 | 413/1554 | chr14 | 104884018 | |||
chr14:104884042 | C | G | 1 | a0001c0087 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1263C>G | p.Ser421Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1536/6727 | 1263/4665 | 421/1554 | chr14 | 104884042 | |||
chr14:104884075 | C | T | 2 | a0001c0065 a0009c0025 |
3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.1296C>T | p.Ala432Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1569/6727 | 1296/4665 | 432/1554 | chr14 | 104884075 | |||
chr14:104884102 | C | T | 3 | a0001c0014 a0001c0048 a0001c0053 |
5 | HG02109.hp2 HG02622.hp1 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.1323C>T | p.Ala441Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1596/6727 | 1323/4665 | 441/1554 | chr14 | 104884102 | |||
chr14:104884411 | G | A | 1 | a0001c0041 | 1 | NA19054.hp1 | synonymous_variant | LOW | c.1632G>A | p.Pro544Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1905/6727 | 1632/4665 | 544/1554 | chr14 | 104884411 | |||
chr14:104884462 | C | T | 43 | a0001c0002 a0001c0003 a0001c0006 others(40): Show |
136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
synonymous_variant | LOW | c.1683C>T | p.Asp561Asp | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 1956/6727 | 1683/4665 | 561/1554 | chr14 | 104884462 | |||
chr14:104884507 | G | A | 1 | a0001c0023 | 2 | NA19007.hp2 NA19087.hp1 |
synonymous_variant | LOW | c.1728G>A | p.Ala576Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 2001/6727 | 1728/4665 | 576/1554 | chr14 | 104884507 | |||
chr14:104884531 | C | T | 43 | a0001c0002 a0001c0003 a0001c0006 others(40): Show |
136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
synonymous_variant | LOW | c.1752C>T | p.Ala584Ala | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/19 | 2025/6727 | 1752/4665 | 584/1554 | chr14 | 104884531 | |||
chr14:104886054 | G | A | 1 | a0001c0059 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1959G>A | p.Pro653Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 11/19 | 2232/6727 | 1959/4665 | 653/1554 | chr14 | 104886054 | |||
chr14:104886591 | C | T | 1 | a0011c0047 | 1 | NA18969.hp1 | synonymous_variant | LOW | c.2352C>T | p.Arg784Arg | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2625/6727 | 2352/4665 | 784/1554 | chr14 | 104886591 | |||
chr14:104886781 | C | T | 1 | a0021c0052 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.2542C>T | p.Leu848Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2815/6727 | 2542/4665 | 848/1554 | chr14 | 104886781 | |||
chr14:104886843 | C | T | 1 | a0001c0037 | 1 | NA18982.hp2 | synonymous_variant | LOW | c.2604C>T | p.Ser868Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 2877/6727 | 2604/4665 | 868/1554 | chr14 | 104886843 | |||
chr14:104887068 | G | A | 2 | a0001c0017 a0001c0019 |
6 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
synonymous_variant | LOW | c.2829G>A | p.Pro943Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3102/6727 | 2829/4665 | 943/1554 | chr14 | 104887068 | |||
chr14:104887644 | A | G | 1 | a0020c0040 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.3405A>G | p.Ser1135Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3678/6727 | 3405/4665 | 1135/1554 | chr14 | 104887644 | |||
chr14:104887956 | A | G | 51 | a0001c0002 a0001c0003 a0001c0005 others(48): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
synonymous_variant | LOW | c.3717A>G | p.Ser1239Ser | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/19 | 3990/6727 | 3717/4665 | 1239/1554 | chr14 | 104887956 | |||
chr14:104893030 | T | C | 1 | a0001c0035 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.3933T>C | p.Asp1311Asp | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/19 | 4206/6727 | 3933/4665 | 1311/1554 | chr14 | 104893030 | |||
chr14:104893790 | G | A | 12 | a0001c0017 a0001c0019 a0001c0020 others(9): Show |
19 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
synonymous_variant | LOW | c.4212G>A | p.Pro1404Pro | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/19 | 4485/6727 | 4212/4665 | 1404/1554 | chr14 | 104893790 | |||
chr14:104894808 | C | G | 1 | a0001c0042 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.4515C>G | p.Arg1505Arg | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 4788/6727 | 4515/4665 | 1505/1554 | chr14 | 104894808 | |||
chr14:104894952 | G | C | 1 | a0001c0058 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.4659G>C | p.Leu1553Leu | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 4932/6727 | 4659/4665 | 1553/1554 | chr14 | 104894952 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104865272 | G | A | 1 | a0029c0033t0009 | 1 | NA19058.hp2 | 5_prime_UTR_variant | MODIFIER | c.-269G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/19 | 3179 | chr14 | 104865272 | ||||||
chr14:104865275 | A | G | 1 | a0001c0001t0027 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-266A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/19 | 3176 | chr14 | 104865275 | ||||||
chr14:104865316 | G | A | 1 | a0001c0001t0010 | 1 | NA18960.hp1 | 5_prime_UTR_variant | MODIFIER | c.-225G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/19 | 3135 | chr14 | 104865316 | ||||||
chr14:104865391 | C | CCGGG | 6 | a0001c0001t0026 a0001c0005t0003 a0001c0008t0003 others(3): Show |
25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-135_-132dupGGCG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/19 | 3041 | INFO_REALIGN_3_PRIME | chr14 | 104865391 | |||||
chr14:104865498 | C | A | 1 | a0020c0040t0011 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/19 | 2953 | chr14 | 104865498 | ||||||
chr14:104895000 | C | G | 1 | a0001c0001t0025 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 42 | chr14 | 104895000 | ||||||
chr14:104895087 | G | A | 8 | a0001c0006t0005 a0001c0006t0007 a0001c0035t0013 others(5): Show |
14 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*129G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 129 | chr14 | 104895087 | ||||||
chr14:104895100 | G | A | 1 | a0005c0016t0014 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*142G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 142 | chr14 | 104895100 | ||||||
chr14:104895251 | G | C | 1 | a0001c0001t0015 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*293G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 293 | chr14 | 104895251 | ||||||
chr14:104895427 | G | A | 1 | a0001c0001t0016 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*469G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 469 | chr14 | 104895427 | ||||||
chr14:104895492 | C | A | 1 | a0001c0061t0017 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*534C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 534 | chr14 | 104895492 | ||||||
chr14:104895511 | C | G | 1 | a0001c0032t0024 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*553C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 553 | chr14 | 104895511 | ||||||
chr14:104895597 | T | C | 56 | a0001c0001t0002 a0001c0001t0015 a0001c0002t0002 others(53): Show |
166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*639T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 639 | chr14 | 104895597 | ||||||
chr14:104895706 | G | A | 1 | a0001c0080t0018 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*748G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 748 | chr14 | 104895706 | ||||||
chr14:104895862 | C | T | 1 | a0001c0003t0022 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*904C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 904 | chr14 | 104895862 | ||||||
chr14:104895869 | T | C | 1 | a0002c0009t0012 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*911T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 911 | chr14 | 104895869 | ||||||
chr14:104895907 | C | T | 8 | a0001c0001t0004 a0001c0001t0016 a0001c0022t0004 others(5): Show |
22 | HG00673.hp1 HG01943.hp2 HG01978.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*949C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 949 | chr14 | 104895907 | ||||||
chr14:104896017 | G | A | 2 | a0004c0021t0006 a0004c0081t0006 |
4 | HG02559.hp1 HG02622.hp2 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1059G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1059 | chr14 | 104896017 | ||||||
chr14:104896096 | G | A | 1 | a0001c0007t0008 | 3 | HG02055.hp2 HG02965.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1138G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1138 | chr14 | 104896096 | ||||||
chr14:104896194 | G | A | 2 | a0001c0006t0007 a0012c0036t0007 |
3 | HG00438.hp1 HG01496.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1236G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1236 | chr14 | 104896194 | ||||||
chr14:104896456 | G | A | 2 | a0001c0035t0013 a0029c0033t0009 |
2 | NA19058.hp2 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1498G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1498 | chr14 | 104896456 | ||||||
chr14:104896482 | C | T | 1 | a0001c0003t0021 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1524C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1524 | chr14 | 104896482 | ||||||
chr14:104896629 | C | T | 1 | a0022c0068t0020 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1671 | chr14 | 104896629 | ||||||
chr14:104896650 | G | A | 1 | a0001c0001t0023 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1692G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 19/19 | 1692 | chr14 | 104896650 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:104865556 | C | T | 1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-28+43C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104865556 | |||||||
chr14:104865596 | C | CG | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0006t0005g0043 others(1): Show |
4 | HG00738.hp1 HG01099.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+87dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 104865596 | ||||||
chr14:104865664 | G | A | 39 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0045 others(36): Show |
47 | HG00140.hp1 HG00280.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.-28+151G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104865664 | |||||||
chr14:104865791 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-28+278A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104865791 | |||||||
chr14:104865955 | C | T | 1 | a0001c0006t0005g0256 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-28+442C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104865955 | |||||||
chr14:104865961 | C | T | 2 | a0001c0065t0002g0255 a0009c0025t0002g0039 |
3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-28+448C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104865961 | |||||||
chr14:104866201 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | NA18945.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.-28+688T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866201 | |||||||
chr14:104866289 | C | A | 1 | a0001c0013t0002g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-28+776C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866289 | |||||||
chr14:104866338 | C | T | 21 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(18): Show |
25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-28+825C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866338 | |||||||
chr14:104866390 | C | T | 2 | a0003c0026t0002g0237 a0003c0078t0002g0236 |
2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-28+877C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866390 | |||||||
chr14:104866457 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-28+944G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866457 | |||||||
chr14:104866467 | C | A | 3 | a0001c0011t0001g0074 a0001c0011t0001g0075 a0024c0050t0001g0073 |
3 | NA18955.hp2 NA19000.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-28+954C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866467 | |||||||
chr14:104866551 | A | AG | 6 | a0001c0001t0001g0017 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
6 | HG00140.hp1 HG01168.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+1041dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr14 | 104866551 | ||||||
chr14:104866633 | T | C | 1 | a0001c0005t0003g0238 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-28+1120T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866633 | |||||||
chr14:104866634 | C | G | 1 | a0009c0025t0002g0039 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-28+1121C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866634 | |||||||
chr14:104866806 | C | A | 1 | a0001c0006t0005g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-28+1293C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866806 | |||||||
chr14:104866881 | C | T | 4 | a0004c0021t0006g0232 a0004c0021t0006g0234 a0004c0021t0006g0235 others(1): Show |
4 | HG02559.hp1 HG02622.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+1368C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866881 | |||||||
chr14:104866918 | C | T | 1 | a0001c0003t0021g0231 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-28+1405C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104866918 | |||||||
chr14:104867202 | A | G | 114 | a0001c0001t0002g0230 a0001c0002t0002g0003 a0001c0002t0002g0004 others(111): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.-27-1222A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867202 | |||||||
chr14:104867226 | C | T | 2 | a0001c0065t0002g0255 a0009c0025t0002g0039 |
3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-27-1198C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867226 | |||||||
chr14:104867307 | C | T | 75 | a0001c0001t0002g0230 a0001c0002t0002g0003 a0001c0002t0002g0004 others(72): Show |
93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-27-1117C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867307 | |||||||
chr14:104867824 | G | A | 2 | a0001c0058t0001g0077 a0001c0059t0001g0078 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-27-600G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867824 | |||||||
chr14:104867859 | C | A | 145 | a0001c0001t0026g0251 a0001c0002t0002g0003 a0001c0002t0002g0004 others(142): Show |
170 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.-27-565C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867859 | |||||||
chr14:104867898 | C | G | 1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-27-526C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104867898 | |||||||
chr14:104868092 | C | T | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-332C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104868092 | |||||||
chr14:104868284 | C | T | 1 | a0001c0041t0001g0145 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-27-140C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104868284 | |||||||
chr14:104868311 | C | T | 21 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(18): Show |
25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-27-113C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 1/18 | chr14 | 104868311 | |||||||
chr14:104868712 | C | T | 75 | a0001c0001t0002g0230 a0001c0002t0002g0003 a0001c0002t0002g0004 others(72): Show |
93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.105+157C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104868712 | |||||||
chr14:104868959 | T | C | 2 | a0001c0014t0001g0018 a0001c0014t0001g0079 |
3 | HG02109.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.105+404T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104868959 | |||||||
chr14:104869183 | G | A | 12 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(9): Show |
13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.105+628G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869183 | |||||||
chr14:104869293 | G | A | 12 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(9): Show |
13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.105+738G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869293 | |||||||
chr14:104869373 | A | G | 118 | a0001c0001t0002g0230 a0001c0002t0002g0003 a0001c0002t0002g0004 others(115): Show |
139 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.105+818A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869373 | |||||||
chr14:104869520 | C | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0144 |
7 | NA18940.hp1 NA18945.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.105+965C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869520 | |||||||
chr14:104869541 | T | C | 25 | a0001c0014t0001g0018 a0001c0014t0001g0079 a0001c0017t0002g0162 others(22): Show |
26 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.105+986T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869541 | |||||||
chr14:104869797 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.105+1242A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869797 | |||||||
chr14:104869799 | T | C | 6 | a0001c0080t0018g0080 a0004c0021t0006g0232 a0004c0021t0006g0234 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.105+1244T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104869799 | |||||||
chr14:104870002 | G | A | 1 | a0001c0020t0002g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.105+1447G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870002 | |||||||
chr14:104870063 | G | A | 1 | a0001c0062t0002g0169 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.105+1508G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870063 | |||||||
chr14:104870093 | C | T | 1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.105+1538C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870093 | |||||||
chr14:104870109 | C | CA | 114 | a0001c0001t0002g0230 a0001c0002t0002g0003 a0001c0002t0002g0004 others(111): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.105+1556dupA | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104870109 | ||||||
chr14:104870210 | G | A | 2 | a0001c0058t0001g0077 a0001c0059t0001g0078 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.105+1655G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870210 | |||||||
chr14:104870227 | C | T | 5 | a0001c0003t0002g0226 a0001c0003t0002g0227 a0001c0003t0002g0228 others(2): Show |
5 | HG01192.hp1 HG01928.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+1672C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870227 | |||||||
chr14:104870414 | G | A | 118 | a0001c0001t0002g0230 a0001c0002t0002g0003 a0001c0002t0002g0004 others(115): Show |
139 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.105+1859G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870414 | |||||||
chr14:104870475 | G | C | 3 | a0001c0014t0001g0018 a0001c0014t0001g0079 a0022c0068t0020g0082 |
4 | HG02109.hp2 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+1920G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870475 | |||||||
chr14:104870478 | C | G | 21 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(18): Show |
25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.105+1923C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870478 | |||||||
chr14:104870528 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.105+1973G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870528 | |||||||
chr14:104870621 | G | A | 1 | a0002c0004t0002g0171 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.105+2066G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870621 | |||||||
chr14:104870645 | G | A | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.105+2090G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870645 | |||||||
chr14:104870682 | C | T | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+2127C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870682 | |||||||
chr14:104870683 | G | A | 1 | a0001c0071t0003g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.105+2128G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870683 | |||||||
chr14:104870847 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.105+2292C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870847 | |||||||
chr14:104870913 | G | T | 14 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0246 others(11): Show |
17 | HG01167.hp2 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.105+2358G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870913 | |||||||
chr14:104870949 | C | T | 22 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(19): Show |
26 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.105+2394C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104870949 | |||||||
chr14:104871150 | C | T | 1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.105+2595C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871150 | |||||||
chr14:104871176 | G | A | 1 | a0003c0078t0002g0236 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.105+2621G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871176 | |||||||
chr14:104871188 | A | G | 40 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(37): Show |
42 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.105+2633A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871188 | |||||||
chr14:104871200 | A | G | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+2645A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871200 | |||||||
chr14:104871261 | G | A | 1 | a0001c0002t0002g0172 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.105+2706G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871261 | |||||||
chr14:104871299 | G | A | 2 | a0001c0014t0001g0018 a0001c0014t0001g0079 |
3 | HG02109.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.105+2744G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871299 | |||||||
chr14:104871383 | C | T | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+2828C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871383 | |||||||
chr14:104871401 | C | G | 1 | a0001c0001t0001g0140 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.105+2846C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871401 | |||||||
chr14:104871466 | C | T | 122 | a0001c0001t0026g0251 a0001c0002t0002g0003 a0001c0002t0002g0004 others(119): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.105+2911C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871466 | |||||||
chr14:104871760 | G | A | 2 | a0001c0001t0001g0083 a0001c0055t0001g0084 |
2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.105+3205G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104871760 | |||||||
chr14:104872087 | T | A | 1 | a0001c0002t0002g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.105+3532T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872087 | |||||||
chr14:104872121 | C | T | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.105+3566C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872121 | |||||||
chr14:104872123 | T | C | 1 | a0002c0009t0012g0175 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.105+3568T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872123 | |||||||
chr14:104872123 | T | TCGTGTGT others(3): Show |
1 | a0001c0007t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.105+3580_105+3589d others(12): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872123 | ||||||
chr14:104872143 | GC | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0014c0045t0001g0137 |
3 | HG00733.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.105+3590delC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872143 | ||||||
chr14:104872144 | CCGTGTGT others(14): Show |
C | 1 | a0001c0001t0001g0128 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.105+3608_105+3628d others(23): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872144 | ||||||
chr14:104872155 | C | CCGT | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0014c0045t0001g0137 |
3 | HG00733.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.105+3600_105+3601i others(5): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872155 | |||||||
chr14:104872187 | T | C | 145 | a0001c0001t0026g0251 a0001c0002t0002g0003 a0001c0002t0002g0004 others(142): Show |
170 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.105+3632T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872187 | |||||||
chr14:104872191 | T | G | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.105+3636T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872191 | |||||||
chr14:104872199 | G | A | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.105+3644G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872199 | |||||||
chr14:104872230 | C | T | 1 | a0016c0084t0002g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.105+3675C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872230 | |||||||
chr14:104872257 | T | G | 1 | a0001c0074t0002g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+3702T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872257 | |||||||
chr14:104872262 | G | A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0086 others(6): Show |
12 | HG01891.hp2 HG02280.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.105+3707G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872262 | |||||||
chr14:104872265 | T | C | 1 | a0001c0074t0002g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+3710T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872265 | |||||||
chr14:104872269 | G | T | 1 | a0001c0074t0002g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+3714G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872269 | |||||||
chr14:104872277 | G | A | 1 | a0001c0054t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.105+3722G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872277 | |||||||
chr14:104872278 | T | C | 1 | a0001c0074t0002g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+3723T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872278 | |||||||
chr14:104872280 | T | G | 5 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 others(2): Show |
5 | HG01099.hp1 HG02735.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+3725T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872280 | |||||||
chr14:104872284 | T | C | 1 | a0001c0001t0004g0016 | 2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.105+3729T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872284 | |||||||
chr14:104872287 | C | CGCGTGTG others(3): Show |
142 | a0001c0001t0026g0251 a0001c0002t0002g0003 a0001c0002t0002g0004 others(139): Show |
167 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.105+3735_105+3744d others(12): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872287 | ||||||
chr14:104872287 | C | T | 1 | a0001c0074t0002g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.105+3732C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872287 | |||||||
chr14:104872318 | C | CCGTGGGT others(3): Show |
91 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(88): Show |
110 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.105+3778_105+3787d others(12): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872318 | ||||||
chr14:104872318 | CCGTGGGT others(13): Show |
C | 1 | a0001c0032t0024g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.105+3768_105+3787d others(22): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872318 | ||||||
chr14:104872333 | GGTGTGCG others(3): Show |
G | 23 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0023 others(20): Show |
27 | HG00438.hp2 HG02135.hp1 HG02165.hp1 others(24): Show |
intron_variant | MODIFIER | c.105+3795_105+3804d others(12): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872333 | ||||||
chr14:104872343 | T | G | 46 | a0001c0001t0004g0005 a0001c0001t0026g0251 a0001c0005t0003g0015 others(43): Show |
50 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.105+3788T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872343 | |||||||
chr14:104872349 | CGTGTGTG others(5): Show |
C | 2 | a0001c0034t0004g0148 a0001c0037t0005g0149 |
2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.105+3795_105+3806d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872349 | |||||||
chr14:104872353 | T | G | 1 | a0003c0026t0002g0237 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.105+3798T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872353 | |||||||
chr14:104872357 | T | C | 2 | a0001c0014t0001g0018 a0001c0014t0001g0079 |
3 | HG02109.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.105+3802T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872357 | |||||||
chr14:104872361 | G | A | 1 | a0001c0088t0002g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.105+3806G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872361 | |||||||
chr14:104872362 | CGT | C | 12 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(9): Show |
13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.105+3815_105+3816d others(4): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872362 | ||||||
chr14:104872364 | T | C | 2 | a0001c0034t0004g0148 a0001c0037t0005g0149 |
2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.105+3809T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872364 | |||||||
chr14:104872364 | TGTGTGTG others(6): Show |
T | 1 | a0001c0059t0001g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+3815_105+3827d others(15): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872364 | ||||||
chr14:104872384 | A | G | 147 | a0001c0001t0026g0251 a0001c0002t0002g0003 a0001c0002t0002g0004 others(144): Show |
172 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.105+3829A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872384 | |||||||
chr14:104872385 | T | TGG | 3 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 |
3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.105+3831_105+3832i others(4): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872385 | ||||||
chr14:104872401 | G | GC | 3 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 |
3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.105+3847dupC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872401 | ||||||
chr14:104872406 | G | C | 3 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 |
3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3850G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872406 | |||||||
chr14:104872411 | G | GT | 3 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 |
3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3845_106-3844i others(3): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872411 | |||||||
chr14:104872412 | C | G | 3 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 |
3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3844C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872412 | |||||||
chr14:104872417 | G | C | 123 | a0001c0001t0026g0251 a0001c0002t0002g0003 a0001c0002t0002g0004 others(120): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.106-3839G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872417 | |||||||
chr14:104872417 | G | T | 3 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 |
3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3839G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872417 | |||||||
chr14:104872421 | TGCC | T | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.106-3833_106-3831d others(5): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872421 | ||||||
chr14:104872423 | C | G | 1 | a0009c0025t0002g0039 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106-3833C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872423 | |||||||
chr14:104872425 | G | A | 3 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 |
3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3831G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872425 | |||||||
chr14:104872428 | C | T | 5 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 others(2): Show |
6 | HG01099.hp1 HG02735.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-3828C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872428 | |||||||
chr14:104872434 | T | C | 3 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 |
3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3822T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872434 | |||||||
chr14:104872435 | G | GTGACATG others(19): Show |
1 | a0002c0060t0002g0177 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.106-3821_106-3820i others(28): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872435 | |||||||
chr14:104872435 | G | GTGCATGT others(18): Show |
20 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(17): Show |
25 | HG00639.hp2 HG00738.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.106-3821_106-3820i others(27): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872435 | |||||||
chr14:104872435 | G | GTGCCATG others(19): Show |
53 | a0001c0002t0002g0004 a0001c0002t0002g0172 a0001c0002t0002g0191 others(50): Show |
66 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.106-3821_106-3820i others(28): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872435 | |||||||
chr14:104872436 | C | T | 3 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 |
3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3820C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872436 | |||||||
chr14:104872436 | CGT | C | 24 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(21): Show |
28 | HG01167.hp2 HG01255.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.106-3812_106-3811d others(4): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872436 | ||||||
chr14:104872440 | T | G | 3 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 |
3 | HG01099.hp1 HG02735.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.106-3816T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872440 | |||||||
chr14:104872448 | A | G | 4 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 others(1): Show |
5 | HG01099.hp1 HG02735.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-3808A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872448 | |||||||
chr14:104872459 | TGTGG | T | 4 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 others(1): Show |
5 | HG01099.hp1 HG02735.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-3793_106-3790d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872459 | ||||||
chr14:104872470 | CGT | C | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.106-3778_106-3777d others(4): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872470 | ||||||
chr14:104872478 | T | C | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106-3778T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872478 | |||||||
chr14:104872479 | G | GC | 4 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 others(1): Show |
5 | HG01099.hp1 HG02735.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-3776dupC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872479 | ||||||
chr14:104872479 | G | GCGTGTGT others(13): Show |
58 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(55): Show |
64 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.106-3758_106-3757i others(22): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872479 | ||||||
chr14:104872479 | G | GTGTGTGC others(11): Show |
1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106-3777_106-3776i others(20): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872479 | |||||||
chr14:104872489 | CGTGT | C | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.106-3759_106-3756d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr14 | 104872489 | ||||||
chr14:104872552 | C | T | 1 | a0001c0015t0001g0066 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.106-3704C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872552 | |||||||
chr14:104872559 | T | TC | 2 | a0001c0065t0002g0255 a0009c0025t0002g0039 |
3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.106-3697_106-3696i others(3): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872559 | |||||||
chr14:104872581 | C | G | 1 | a0001c0007t0008g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.106-3675C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872581 | |||||||
chr14:104872605 | G | A | 1 | a0001c0013t0002g0044 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.106-3651G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872605 | |||||||
chr14:104872661 | G | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0014c0045t0001g0137 |
3 | HG00733.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.106-3595G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872661 | |||||||
chr14:104872690 | C | T | 1 | a0001c0003t0002g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.106-3566C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872690 | |||||||
chr14:104872691 | G | A | 1 | a0001c0003t0002g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.106-3565G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872691 | |||||||
chr14:104872717 | G | A | 6 | a0001c0006t0005g0028 a0001c0006t0007g0029 a0001c0035t0013g0150 others(3): Show |
7 | HG00438.hp1 HG01496.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-3539G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872717 | |||||||
chr14:104872821 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.106-3435C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872821 | |||||||
chr14:104872836 | C | G | 1 | a0001c0032t0024g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.106-3420C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872836 | |||||||
chr14:104872911 | G | A | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106-3345G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872911 | |||||||
chr14:104872947 | T | C | 67 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(64): Show |
85 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.106-3309T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104872947 | |||||||
chr14:104873223 | G | C | 71 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0049 others(68): Show |
88 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.106-3033G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873223 | |||||||
chr14:104873310 | A | G | 21 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(18): Show |
25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.106-2946A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873310 | |||||||
chr14:104873331 | G | A | 1 | a0001c0002t0002g0191 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.106-2925G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873331 | |||||||
chr14:104873442 | T | C | 2 | a0001c0058t0001g0077 a0001c0059t0001g0078 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.106-2814T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873442 | |||||||
chr14:104873631 | T | C | 95 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(92): Show |
114 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.106-2625T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873631 | |||||||
chr14:104873647 | G | A | 1 | a0016c0084t0002g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.106-2609G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873647 | |||||||
chr14:104873675 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.106-2581C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873675 | |||||||
chr14:104873676 | G | T | 1 | a0001c0001t0023g0090 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.106-2580G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873676 | |||||||
chr14:104873786 | C | T | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106-2470C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873786 | |||||||
chr14:104873793 | C | T | 124 | a0001c0001t0026g0251 a0001c0002t0002g0003 a0001c0002t0002g0004 others(121): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.106-2463C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873793 | |||||||
chr14:104873841 | G | C | 1 | a0001c0011t0001g0101 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.106-2415G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104873841 | |||||||
chr14:104874033 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0144 |
5 | NA18940.hp1 NA18947.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.106-2223C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874033 | |||||||
chr14:104874173 | C | T | 7 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0132 others(4): Show |
7 | HG00639.hp1 HG01175.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.106-2083C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874173 | |||||||
chr14:104874234 | C | T | 2 | a0001c0014t0001g0018 a0001c0014t0001g0079 |
3 | HG02109.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.106-2022C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874234 | |||||||
chr14:104874306 | C | T | 145 | a0001c0001t0026g0251 a0001c0002t0002g0003 a0001c0002t0002g0004 others(142): Show |
170 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.106-1950C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874306 | |||||||
chr14:104874656 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.106-1600A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874656 | |||||||
chr14:104874661 | C | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0014c0045t0001g0137 |
3 | HG00733.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.106-1595C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874661 | |||||||
chr14:104874713 | C | A | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-1543C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874713 | |||||||
chr14:104874763 | T | A | 138 | a0001c0001t0026g0251 a0001c0002t0002g0003 a0001c0002t0002g0004 others(135): Show |
163 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.106-1493T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874763 | |||||||
chr14:104874773 | A | C | 138 | a0001c0001t0026g0251 a0001c0002t0002g0003 a0001c0002t0002g0004 others(135): Show |
163 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.106-1483A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874773 | |||||||
chr14:104874940 | A | G | 7 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0132 others(4): Show |
7 | HG00639.hp1 HG01175.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.106-1316A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104874940 | |||||||
chr14:104875165 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.106-1091C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875165 | |||||||
chr14:104875221 | G | A | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-1035G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875221 | |||||||
chr14:104875391 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.106-865G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875391 | |||||||
chr14:104875464 | C | G | 1 | a0001c0005t0003g0244 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.106-792C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875464 | |||||||
chr14:104875514 | G | A | 1 | a0001c0054t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.106-742G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875514 | |||||||
chr14:104875529 | G | A | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.106-727G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875529 | |||||||
chr14:104875559 | C | T | 3 | a0001c0002t0002g0032 a0001c0002t0002g0184 a0001c0002t0002g0185 |
4 | HG02015.hp1 HG02129.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-697C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875559 | |||||||
chr14:104875560 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.106-696G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875560 | |||||||
chr14:104875621 | T | C | 21 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(18): Show |
25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.106-635T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875621 | |||||||
chr14:104875631 | G | A | 2 | a0013c0039t0001g0102 a0017c0043t0001g0098 |
2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.106-625G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875631 | |||||||
chr14:104875654 | C | T | 2 | a0003c0026t0002g0237 a0003c0078t0002g0236 |
2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.106-602C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875654 | |||||||
chr14:104875924 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG01167.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.106-332G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104875924 | |||||||
chr14:104876010 | G | A | 2 | a0001c0014t0001g0018 a0001c0014t0001g0079 |
3 | HG02109.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.106-246G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104876010 | |||||||
chr14:104876170 | G | T | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-86G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 2/18 | chr14 | 104876170 | |||||||
chr14:104876500 | C | T | 2 | a0001c0001t0002g0230 a0001c0011t0001g0126 |
2 | HG01361.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.195+155C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876500 | |||||||
chr14:104876509 | A | T | 75 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(72): Show |
93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.195+164A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876509 | |||||||
chr14:104876538 | T | C | 45 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(42): Show |
50 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.195+193T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876538 | |||||||
chr14:104876583 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.195+238C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876583 | |||||||
chr14:104876644 | C | G | 75 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(72): Show |
93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.195+299C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876644 | |||||||
chr14:104876645 | A | G | 75 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(72): Show |
93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.195+300A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876645 | |||||||
chr14:104876707 | G | C | 4 | a0004c0021t0006g0232 a0004c0021t0006g0234 a0004c0021t0006g0235 others(1): Show |
4 | HG02559.hp1 HG02622.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+362G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876707 | |||||||
chr14:104876708 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.195+363C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876708 | |||||||
chr14:104876769 | C | T | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+424C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104876769 | |||||||
chr14:104877035 | G | A | 4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0132 others(1): Show |
4 | HG00639.hp1 HG01175.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+690G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877035 | |||||||
chr14:104877057 | ACT | A | 45 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(42): Show |
50 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.195+715_195+716del others(2): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877057 | ||||||
chr14:104877182 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.196-703G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877182 | |||||||
chr14:104877190 | C | A | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-695C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877190 | |||||||
chr14:104877256 | A | G | 88 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(85): Show |
107 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.196-629A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877256 | |||||||
chr14:104877349 | G | A | 24 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(21): Show |
25 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.196-536G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877349 | |||||||
chr14:104877410 | G | T | 1 | a0001c0041t0001g0145 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.196-475G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877410 | |||||||
chr14:104877447 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0023g0090 a0001c0007t0001g0019 others(1): Show |
6 | HG01891.hp2 HG02622.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-438G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877447 | |||||||
chr14:104877512 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.196-373C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877512 | |||||||
chr14:104877774 | G | A | 73 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(70): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.196-111G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877774 | |||||||
chr14:104877805 | G | A | 45 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(42): Show |
50 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.196-80G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877805 | |||||||
chr14:104877820 | G | A | 73 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(70): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.196-65G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877820 | |||||||
chr14:104877845 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0045 others(23): Show |
33 | HG00140.hp1 HG00673.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.196-40C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877845 | |||||||
chr14:104877851 | T | TC | 83 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(80): Show |
98 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.196-20dupC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877851 | ||||||
chr14:104877851 | T | TCC | 26 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0021 others(23): Show |
32 | HG00140.hp1 HG00621.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.196-21_196-20dupCC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877851 | ||||||
chr14:104877851 | TC | T | 19 | a0001c0001t0001g0052 a0001c0001t0001g0089 a0001c0001t0027g0125 others(16): Show |
20 | HG00438.hp1 HG01069.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.196-20delC | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877851 | ||||||
chr14:104877851 | TCCC | T | 15 | a0001c0003t0002g0179 a0001c0003t0002g0186 a0001c0006t0005g0043 others(12): Show |
16 | HG01099.hp1 HG01261.hp2 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.196-22_196-20delCC others(1): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877851 | ||||||
chr14:104877851 | TCCCC | T | 66 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(63): Show |
84 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.196-23_196-20delCC others(2): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr14 | 104877851 | ||||||
chr14:104877858 | C | G | 1 | a0001c0007t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.196-27C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 3/18 | chr14 | 104877858 | |||||||
chr14:104877981 | G | A | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.274+18G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104877981 | |||||||
chr14:104878010 | C | G | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.274+47C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878010 | |||||||
chr14:104878082 | A | G | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.274+119A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878082 | |||||||
chr14:104878141 | C | T | 1 | a0002c0060t0002g0177 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.274+178C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878141 | |||||||
chr14:104878176 | G | A | 1 | a0001c0020t0002g0152 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.274+213G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878176 | |||||||
chr14:104878196 | C | T | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.274+233C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878196 | |||||||
chr14:104878231 | C | T | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.275-212C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878231 | |||||||
chr14:104878254 | C | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0089 |
3 | HG02970.hp2 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.275-189C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878254 | |||||||
chr14:104878266 | C | T | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.275-177C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878266 | |||||||
chr14:104878402 | C | T | 2 | a0002c0004t0002g0213 a0002c0012t0002g0214 |
2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.275-41C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878402 | |||||||
chr14:104878424 | C | T | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.275-19C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 4/18 | chr14 | 104878424 | |||||||
chr14:104878535 | C | T | 46 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(43): Show |
55 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.333+34C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878535 | |||||||
chr14:104878536 | G | A | 1 | a0001c0007t0008g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.333+35G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878536 | |||||||
chr14:104878546 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.333+45C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878546 | |||||||
chr14:104878609 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0091 a0001c0001t0001g0095 |
4 | NA19000.hp1 NA19007.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+108G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878609 | |||||||
chr14:104878698 | C | A | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.333+197C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878698 | |||||||
chr14:104878722 | A | ACAGGTGG others(16): Show |
13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+223_333+245dup others(23): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr14 | 104878722 | ||||||
chr14:104878731 | G | A | 21 | a0001c0017t0002g0162 a0001c0017t0002g0165 a0001c0017t0002g0166 others(18): Show |
21 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.333+230G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878731 | |||||||
chr14:104878745 | G | A | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.333+244G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878745 | |||||||
chr14:104878787 | G | A | 1 | a0032c0072t0002g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.333+286G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878787 | |||||||
chr14:104878806 | G | T | 1 | a0001c0053t0001g0085 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.333+305G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878806 | |||||||
chr14:104878870 | A | G | 13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+369A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878870 | |||||||
chr14:104878896 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.333+395G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878896 | |||||||
chr14:104878939 | G | A | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.333+438G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878939 | |||||||
chr14:104878975 | C | T | 21 | a0001c0001t0026g0251 a0001c0005t0003g0015 a0001c0005t0003g0038 others(18): Show |
25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.333+474C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878975 | |||||||
chr14:104878994 | T | C | 137 | a0001c0001t0026g0251 a0001c0002t0002g0003 a0001c0002t0002g0004 others(134): Show |
162 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.333+493T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104878994 | |||||||
chr14:104879102 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0132 |
3 | HG00639.hp1 HG01175.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.333+601G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879102 | |||||||
chr14:104879198 | G | A | 1 | a0001c0038t0005g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.333+697G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879198 | |||||||
chr14:104879271 | G | A | 13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+770G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879271 | |||||||
chr14:104879444 | G | A | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-843G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879444 | |||||||
chr14:104879461 | G | A | 13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-826G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879461 | |||||||
chr14:104879469 | A | G | 1 | a0008c0027t0003g0250 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.334-818A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879469 | |||||||
chr14:104879753 | C | T | 1 | a0018c0079t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.334-534C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879753 | |||||||
chr14:104879796 | A | G | 263 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(260): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.334-491A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879796 | |||||||
chr14:104879818 | A | G | 6 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0005t0003g0244 others(3): Show |
6 | HG01099.hp2 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-469A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879818 | |||||||
chr14:104879865 | C | T | 1 | a0001c0059t0001g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.334-422C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879865 | |||||||
chr14:104879866 | G | A | 18 | a0001c0006t0005g0028 a0001c0006t0005g0146 a0001c0006t0005g0256 others(15): Show |
19 | HG00438.hp1 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.334-421G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879866 | |||||||
chr14:104879887 | C | T | 1 | a0002c0004t0002g0189 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.334-400C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879887 | |||||||
chr14:104879903 | C | T | 93 | a0001c0002t0002g0004 a0001c0002t0002g0033 a0001c0002t0002g0034 others(90): Show |
111 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.334-384C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879903 | |||||||
chr14:104879946 | G | T | 23 | a0001c0003t0002g0211 a0001c0005t0003g0038 a0001c0005t0003g0238 others(20): Show |
27 | HG01167.hp2 HG01255.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.334-341G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104879946 | |||||||
chr14:104880108 | G | A | 2 | a0001c0001t0004g0061 a0002c0012t0002g0197 |
2 | HG02735.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.334-179G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104880108 | |||||||
chr14:104880112 | C | T | 13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-175C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 5/18 | chr14 | 104880112 | |||||||
chr14:104880485 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0124 |
2 | NA19063.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.472+60C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880485 | |||||||
chr14:104880490 | C | T | 1 | a0002c0028t0002g0204 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.472+65C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880490 | |||||||
chr14:104880532 | G | A | 13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.472+107G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880532 | |||||||
chr14:104880570 | T | C | 131 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(128): Show |
155 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.472+145T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880570 | |||||||
chr14:104880597 | T | C | 1 | a0001c0002t0002g0185 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.472+172T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880597 | |||||||
chr14:104880688 | C | G | 4 | a0001c0005t0003g0238 a0001c0005t0003g0242 a0001c0005t0003g0243 others(1): Show |
4 | HG01255.hp1 HG02258.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.472+263C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880688 | |||||||
chr14:104880693 | A | C | 1 | a0001c0001t0001g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.472+268A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880693 | |||||||
chr14:104880808 | A | C | 1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.472+383A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880808 | |||||||
chr14:104880898 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.472+473A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880898 | |||||||
chr14:104880911 | C | G | 53 | a0001c0005t0003g0015 a0001c0005t0003g0038 a0001c0005t0003g0238 others(50): Show |
57 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.472+486C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880911 | |||||||
chr14:104880959 | G | A | 14 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(11): Show |
15 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.472+534G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104880959 | |||||||
chr14:104881021 | G | A | 2 | a0001c0058t0001g0077 a0001c0059t0001g0078 |
2 | HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.472+596G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881021 | |||||||
chr14:104881085 | G | T | 1 | a0001c0002t0002g0210 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.472+660G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881085 | |||||||
chr14:104881103 | G | A | 1 | a0001c0003t0002g0180 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.472+678G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881103 | |||||||
chr14:104881151 | C | T | 112 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0115 others(109): Show |
135 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.472+726C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881151 | |||||||
chr14:104881197 | G | C | 1 | a0001c0017t0002g0162 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.472+772G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881197 | |||||||
chr14:104881351 | G | A | 11 | a0001c0003t0002g0207 a0001c0006t0005g0028 a0001c0006t0005g0043 others(8): Show |
11 | HG01099.hp1 HG01109.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.472+926G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881351 | |||||||
chr14:104881627 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.473-1101G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881627 | |||||||
chr14:104881658 | G | C | 1 | a0001c0011t0001g0117 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.473-1070G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881658 | |||||||
chr14:104881676 | G | A | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.473-1052G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881676 | |||||||
chr14:104881681 | A | C | 2 | a0001c0034t0004g0148 a0001c0037t0005g0149 |
2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.473-1047A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881681 | |||||||
chr14:104881681 | A | G | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.473-1047A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881681 | |||||||
chr14:104881684 | G | A | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.473-1044G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881684 | |||||||
chr14:104881702 | G | A | 73 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(70): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.473-1026G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881702 | |||||||
chr14:104881714 | A | G | 139 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(136): Show |
163 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.473-1014A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881714 | |||||||
chr14:104881823 | G | A | 12 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(9): Show |
12 | HG01099.hp1 HG01516.hp1 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.473-905G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881823 | |||||||
chr14:104881884 | G | C | 1 | a0002c0009t0002g0201 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.473-844G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881884 | |||||||
chr14:104881910 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.473-818A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881910 | |||||||
chr14:104881934 | C | T | 13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.473-794C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881934 | |||||||
chr14:104881997 | C | T | 19 | a0001c0017t0002g0162 a0001c0017t0002g0165 a0001c0017t0002g0166 others(16): Show |
19 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.473-731C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104881997 | |||||||
chr14:104882001 | C | G | 13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.473-727C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882001 | |||||||
chr14:104882038 | A | C | 2 | a0001c0005t0003g0242 a0001c0005t0003g0243 |
2 | HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.473-690A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882038 | |||||||
chr14:104882161 | T | C | 21 | a0001c0005t0003g0015 a0001c0005t0003g0038 a0001c0005t0003g0238 others(18): Show |
25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.473-567T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882161 | |||||||
chr14:104882188 | G | T | 1 | a0002c0004t0002g0203 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.473-540G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882188 | |||||||
chr14:104882215 | C | T | 95 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(92): Show |
117 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.473-513C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882215 | |||||||
chr14:104882225 | A | G | 21 | a0001c0005t0003g0015 a0001c0005t0003g0038 a0001c0005t0003g0238 others(18): Show |
25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.473-503A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882225 | |||||||
chr14:104882227 | GT | G | 21 | a0001c0005t0003g0015 a0001c0005t0003g0038 a0001c0005t0003g0238 others(18): Show |
25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.473-500delT | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882227 | |||||||
chr14:104882379 | T | G | 2 | a0003c0026t0002g0030 a0003c0067t0002g0030 |
2 | HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.473-349T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882379 | |||||||
chr14:104882387 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.473-341G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882387 | |||||||
chr14:104882396 | G | T | 102 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(99): Show |
123 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.473-332G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882396 | |||||||
chr14:104882433 | A | G | 13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.473-295A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882433 | |||||||
chr14:104882435 | A | G | 1 | a0002c0029t0002g0037 | 2 | HG01361.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.473-293A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882435 | |||||||
chr14:104882447 | AGAGGAGG others(11): Show |
A | 2 | a0001c0061t0017g0170 a0001c0062t0002g0169 |
2 | HG01496.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.473-262_473-245del others(18): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 104882447 | ||||||
chr14:104882466 | GAGGAGGG others(11): Show |
G | 2 | a0001c0065t0002g0255 a0009c0025t0002g0039 |
3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.473-258_473-241del others(18): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr14 | 104882466 | ||||||
chr14:104882513 | G | C | 1 | a0001c0001t0004g0065 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.473-215G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 6/18 | chr14 | 104882513 | |||||||
chr14:104882849 | G | C | 3 | a0001c0019t0002g0159 a0001c0019t0002g0160 a0001c0019t0002g0164 |
3 | HG00733.hp2 HG01123.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.577+17G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 7/18 | chr14 | 104882849 | |||||||
chr14:104882883 | T | G | 132 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(129): Show |
156 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.577+51T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 7/18 | chr14 | 104882883 | |||||||
chr14:104882933 | G | A | 1 | a0001c0032t0024g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.577+101G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 7/18 | chr14 | 104882933 | |||||||
chr14:104883529 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1051+21C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883529 | |||||||
chr14:104883540 | C | T | 124 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(121): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.1051+32C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883540 | |||||||
chr14:104883549 | C | T | 128 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(125): Show |
152 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.1051+41C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883549 | |||||||
chr14:104883554 | G | A | 74 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(71): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1051+46G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883554 | |||||||
chr14:104883560 | A | G | 129 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(126): Show |
153 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1051+52A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883560 | |||||||
chr14:104883683 | G | A | 2 | a0001c0002t0002g0174 a0001c0003t0002g0181 |
2 | HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1052-148G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883683 | |||||||
chr14:104883709 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1052-122G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883709 | |||||||
chr14:104883712 | C | G | 1 | a0018c0079t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1052-119C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883712 | |||||||
chr14:104883796 | C | T | 5 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 others(2): Show |
5 | HG01099.hp1 HG02735.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052-35C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 8/18 | chr14 | 104883796 | |||||||
chr14:104884561 | C | CGGCGAGT others(354): Show |
1 | a0001c0022t0004g0199 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1770+204_1770+205i others(363): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884561 | ||||||
chr14:104884561 | CGGCGAGT others(45): Show |
C | 1 | a0026c0076t0004g0063 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1770+45_1770+96del others(52): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884561 | ||||||
chr14:104884576 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG01167.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1770+27C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884576 | |||||||
chr14:104884579 | G | A | 22 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0023 others(19): Show |
25 | HG00438.hp2 HG00673.hp1 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.1770+30G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884579 | |||||||
chr14:104884587 | CG | C | 23 | a0001c0001t0001g0105 a0001c0005t0003g0015 a0001c0005t0003g0038 others(20): Show |
27 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1770+45delG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884587 | ||||||
chr14:104884588 | G | GGGGGGGT others(44): Show |
9 | a0001c0002t0002g0032 a0001c0020t0002g0031 a0001c0020t0002g0152 others(6): Show |
9 | HG02129.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1770+103_1770+153d others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884588 | ||||||
chr14:104884588 | G | GGGGGGGT others(96): Show |
1 | a0003c0026t0002g0237 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1770+96_1770+97ins others(103): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884588 | ||||||
chr14:104884593 | G | A | 12 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(9): Show |
13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1770+44G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884593 | |||||||
chr14:104884601 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1770+52C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884601 | |||||||
chr14:104884607 | C | CG | 5 | a0001c0001t0001g0142 a0001c0008t0003g0252 a0007c0024t0001g0093 others(2): Show |
5 | HG02055.hp1 HG03486.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770+63dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884607 | ||||||
chr14:104884652 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1770+103C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884652 | |||||||
chr14:104884652 | CGATGCCG others(199): Show |
C | 12 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0042 others(9): Show |
15 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1770+180_1770+385d others(2): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884652 | ||||||
chr14:104884653 | G | A | 1 | a0003c0026t0002g0237 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1770+104G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884653 | |||||||
chr14:104884653 | G | GATGCCGG others(44): Show |
5 | a0001c0017t0002g0165 a0001c0017t0002g0166 a0001c0019t0002g0159 others(2): Show |
5 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770+153_1770+154i others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884653 | ||||||
chr14:104884669 | A | G | 1 | a0001c0070t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1770+120A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884669 | |||||||
chr14:104884690 | CGGGGGGT others(96): Show |
C | 18 | a0001c0002t0002g0004 a0001c0002t0002g0191 a0001c0002t0002g0210 others(15): Show |
23 | HG00140.hp2 HG00438.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1770+193_1770+295d others(2): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884690 | ||||||
chr14:104884690 | CGGGGGGT others(148): Show |
C | 2 | a0001c0003t0002g0183 a0001c0003t0002g0188 |
2 | NA20905.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1770+193_1770+347d others(2): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884690 | ||||||
chr14:104884691 | G | C | 6 | a0001c0001t0001g0105 a0001c0003t0002g0218 a0001c0003t0002g0222 others(3): Show |
6 | HG01109.hp2 HG01192.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1770+142G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884691 | |||||||
chr14:104884691 | GGGGGGTG others(44): Show |
G | 4 | a0001c0082t0002g0033 a0002c0028t0002g0192 a0002c0064t0002g0163 others(1): Show |
4 | HG02698.hp1 HG03654.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1770+193_1770+243d others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884691 | ||||||
chr14:104884703 | T | C | 93 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(90): Show |
108 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1770+154T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884703 | |||||||
chr14:104884703 | T | TGATGCCG others(44): Show |
1 | a0001c0001t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1770+192_1770+193i others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884703 | ||||||
chr14:104884703 | T | TGATGCCG others(180): Show |
1 | a0001c0003t0002g0218 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1770+192_1770+193i others(189): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884703 | ||||||
chr14:104884703 | T | TGATGCCG others(179): Show |
4 | a0001c0003t0002g0222 a0001c0003t0002g0227 a0001c0003t0002g0228 others(1): Show |
4 | HG01192.hp1 HG01928.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1770+192_1770+193i others(188): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884703 | ||||||
chr14:104884718 | C | T | 1 | a0011c0047t0004g0005 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1770+169C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884718 | |||||||
chr14:104884729 | C | A | 1 | a0016c0084t0002g0223 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1770+180C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884729 | |||||||
chr14:104884741 | C | CG | 4 | a0001c0003t0002g0003 a0001c0074t0002g0153 a0001c0087t0002g0195 others(1): Show |
4 | HG01175.hp1 HG01261.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1770+192_1770+193i others(3): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884741 | |||||||
chr14:104884741 | C | CGGGGGGG others(148): Show |
1 | a0001c0001t0001g0105 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1770+192_1770+193i others(157): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884741 | |||||||
chr14:104884741 | C | CGGGGGGT others(147): Show |
1 | a0003c0078t0002g0236 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1770+192_1770+193i others(156): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884741 | |||||||
chr14:104884741 | C | CGGGGGGT others(199): Show |
2 | a0003c0026t0002g0030 a0003c0067t0002g0030 |
2 | HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1770+192_1770+193i others(208): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884741 | |||||||
chr14:104884741 | CCGGGGGT others(45): Show |
C | 46 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0172 others(43): Show |
57 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1770+193_1770+244d others(54): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884741 | |||||||
chr14:104884742 | C | CGGGGGTG others(96): Show |
5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG02559.hp2 HG02683.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1770+199_1770+301d others(105): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884742 | ||||||
chr14:104884742 | C | G | 31 | a0001c0001t0001g0105 a0001c0002t0002g0033 a0001c0002t0002g0034 others(28): Show |
34 | HG00642.hp1 HG01081.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.1770+193C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884742 | |||||||
chr14:104884742 | CGGGGGTG others(45): Show |
C | 15 | a0001c0001t0001g0021 a0001c0001t0001g0041 a0001c0001t0001g0089 others(12): Show |
17 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1770+302_1770+353d others(54): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884742 | ||||||
chr14:104884754 | T | C | 28 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0182 others(25): Show |
31 | HG00642.hp1 HG01081.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1770+205T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884754 | |||||||
chr14:104884780 | C | A | 1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1770+231C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884780 | |||||||
chr14:104884792 | C | CCGGGGGT others(95): Show |
1 | a0002c0012t0002g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1770+243_1770+244i others(104): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884792 | |||||||
chr14:104884792 | CG | C | 28 | a0001c0003t0002g0190 a0001c0003t0002g0211 a0001c0003t0002g0218 others(25): Show |
31 | HG01081.hp1 HG01106.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1770+250delG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884792 | ||||||
chr14:104884793 | G | C | 1 | a0002c0012t0002g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1770+244G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884793 | |||||||
chr14:104884793 | G | GGGGGGGT others(44): Show |
14 | a0001c0017t0002g0162 a0001c0017t0002g0165 a0001c0017t0002g0166 others(11): Show |
14 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1770+251_1770+301d others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884793 | ||||||
chr14:104884793 | G | GGGGGGTG others(94): Show |
1 | a0002c0012t0002g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1770+249_1770+250i others(103): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884793 | ||||||
chr14:104884793 | G | GGGGGGTG others(504): Show |
1 | a0001c0003t0002g0003 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1770+249_1770+250i others(513): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884793 | ||||||
chr14:104884793 | G | GGGGGGTG others(351): Show |
1 | a0001c0087t0002g0195 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1770+249_1770+250i others(360): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884793 | ||||||
chr14:104884794 | G | C | 8 | a0001c0015t0001g0104 a0001c0061t0017g0170 a0001c0062t0002g0169 others(5): Show |
9 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1770+245G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884794 | |||||||
chr14:104884794 | G | GGGGGTGG others(94): Show |
1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1770+249_1770+250i others(103): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884794 | ||||||
chr14:104884795 | G | T | 1 | a0011c0047t0004g0005 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1770+246G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884795 | |||||||
chr14:104884806 | T | C | 78 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(75): Show |
96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1770+257T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884806 | |||||||
chr14:104884806 | T | TGATGCCG others(197): Show |
1 | a0006c0030t0002g0176 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1770+301_1770+302i others(206): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884806 | ||||||
chr14:104884806 | T | TGATGCCG others(146): Show |
1 | a0001c0010t0002g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1770+301_1770+302i others(155): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884806 | ||||||
chr14:104884812 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1770+263C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884812 | |||||||
chr14:104884813 | GGGGGTGG others(44): Show |
G | 1 | a0001c0002t0002g0182 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1770+269_1770+319d others(53): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884813 | ||||||
chr14:104884832 | C | A | 2 | a0002c0004t0002g0171 a0002c0004t0002g0173 |
2 | HG01106.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1770+283C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884832 | |||||||
chr14:104884844 | C | T | 1 | a0001c0032t0024g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1770+295C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884844 | |||||||
chr14:104884844 | CG | C | 19 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0216 others(16): Show |
23 | HG00642.hp1 HG00733.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1770+302delG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884844 | ||||||
chr14:104884845 | G | GGGGGGGT others(95): Show |
1 | a0001c0003t0002g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1770+308_1770+309i others(104): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884845 | ||||||
chr14:104884845 | G | GGGGGGTG others(43): Show |
1 | a0001c0032t0024g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1770+301_1770+302i others(52): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884845 | ||||||
chr14:104884845 | G | GGGGGGTG others(455): Show |
1 | a0001c0083t0002g0212 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1770+301_1770+302i others(464): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884845 | ||||||
chr14:104884858 | T | C | 10 | a0001c0003t0002g0183 a0001c0003t0002g0188 a0001c0003t0002g0190 others(7): Show |
10 | HG01081.hp1 HG01099.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.1770+309T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884858 | |||||||
chr14:104884884 | C | A | 3 | a0001c0065t0002g0255 a0009c0025t0002g0039 a0014c0045t0001g0137 |
4 | HG00733.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1770+335C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884884 | |||||||
chr14:104884896 | C | CGGGGGGG others(45): Show |
1 | a0001c0001t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1770+302_1770+353d others(54): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884896 | ||||||
chr14:104884896 | C | CGGGGGGG others(97): Show |
1 | a0001c0001t0001g0054 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1770+250_1770+353d others(106): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884896 | ||||||
chr14:104884896 | C | CGGGGGGT others(96): Show |
1 | a0001c0015t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1770+385_1770+386i others(105): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884896 | ||||||
chr14:104884896 | C | T | 20 | a0001c0017t0002g0162 a0001c0017t0002g0165 a0001c0017t0002g0166 others(17): Show |
20 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770+347C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884896 | |||||||
chr14:104884897 | G | C | 2 | a0001c0083t0002g0212 a0022c0068t0020g0082 |
2 | HG01099.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1770+348G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884897 | |||||||
chr14:104884897 | G | GGGGGGGT others(249): Show |
4 | a0001c0005t0003g0038 a0001c0005t0003g0241 a0001c0005t0003g0246 others(1): Show |
5 | HG02258.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770+353_1770+354i others(258): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884897 | ||||||
chr14:104884897 | G | GGGGGGGT others(402): Show |
1 | a0001c0005t0003g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1770+353_1770+354i others(411): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884897 | ||||||
chr14:104884897 | G | GGGGGGGT others(352): Show |
4 | a0001c0008t0003g0247 a0001c0008t0003g0248 a0001c0018t0003g0014 others(1): Show |
6 | HG01167.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1770+353_1770+354i others(361): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884897 | ||||||
chr14:104884902 | G | A | 1 | a0001c0032t0024g0167 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1770+353G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884902 | |||||||
chr14:104884909 | T | C | 18 | a0001c0003t0002g0183 a0001c0003t0002g0188 a0001c0003t0002g0190 others(15): Show |
22 | HG00733.hp1 HG01081.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1770+360T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884909 | |||||||
chr14:104884909 | T | TGATGCCG others(301): Show |
1 | a0001c0008t0003g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1770+371_1770+372i others(310): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884909 | ||||||
chr14:104884909 | T | TGATGCCG others(303): Show |
1 | a0008c0027t0003g0249 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1770+385_1770+386i others(312): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884909 | ||||||
chr14:104884909 | T | TGATGCCG others(300): Show |
10 | a0001c0005t0003g0015 a0001c0005t0003g0238 a0001c0005t0003g0242 others(7): Show |
11 | HG01255.hp1 HG02258.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1770+385_1770+386i others(309): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884909 | ||||||
chr14:104884909 | T | TGATGCCG others(197): Show |
1 | a0004c0021t0006g0232 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1770+385_1770+386i others(206): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104884909 | ||||||
chr14:104884934 | C | T | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1770+385C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884934 | |||||||
chr14:104884935 | A | C | 9 | a0001c0001t0027g0125 a0001c0002t0002g0033 a0001c0002t0002g0034 others(6): Show |
10 | HG00733.hp1 HG01257.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1770+386A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884935 | |||||||
chr14:104884947 | C | T | 2 | a0001c0058t0001g0077 a0014c0045t0001g0137 |
2 | HG00733.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1770+398C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884947 | |||||||
chr14:104884948 | G | C | 1 | a0014c0045t0001g0137 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1770+399G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884948 | |||||||
chr14:104884955 | G | A | 1 | a0001c0005t0003g0240 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1770+406G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884955 | |||||||
chr14:104884960 | C | T | 2 | a0001c0015t0001g0104 a0022c0068t0020g0082 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1771-409C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884960 | |||||||
chr14:104884967 | G | A | 2 | a0001c0054t0001g0081 a0021c0052t0001g0055 |
2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1771-402G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884967 | |||||||
chr14:104884975 | C | T | 2 | a0001c0001t0004g0011 a0001c0023t0004g0011 |
3 | NA19007.hp2 NA19010.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1771-394C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884975 | |||||||
chr14:104884985 | C | T | 1 | a0014c0045t0001g0137 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1771-384C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884985 | |||||||
chr14:104884986 | C | A | 2 | a0014c0045t0001g0137 a0022c0068t0020g0082 |
2 | HG00733.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1771-383C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884986 | |||||||
chr14:104884998 | T | C | 2 | a0014c0045t0001g0137 a0022c0068t0020g0082 |
2 | HG00733.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1771-371T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884998 | |||||||
chr14:104884999 | C | G | 2 | a0014c0045t0001g0137 a0022c0068t0020g0082 |
2 | HG00733.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1771-370C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104884999 | |||||||
chr14:104885004 | G | A | 1 | a0001c0058t0001g0077 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1771-365G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885004 | |||||||
chr14:104885005 | T | G | 1 | a0001c0015t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1771-364T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885005 | |||||||
chr14:104885018 | G | A | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1771-351G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885018 | |||||||
chr14:104885030 | T | A | 1 | a0001c0007t0001g0019 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1771-339T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885030 | |||||||
chr14:104885036 | T | C | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1771-333T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885036 | |||||||
chr14:104885049 | C | CG | 8 | a0001c0001t0001g0118 a0001c0003t0002g0178 a0001c0003t0002g0218 others(5): Show |
8 | HG01109.hp2 HG01192.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1771-314dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr14 | 104885049 | ||||||
chr14:104885103 | G | C | 117 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(114): Show |
138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1771-266G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885103 | |||||||
chr14:104885242 | G | A | 12 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(9): Show |
13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1771-127G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885242 | |||||||
chr14:104885267 | G | A | 1 | a0001c0066t0001g0114 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1771-102G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885267 | |||||||
chr14:104885300 | A | G | 139 | a0001c0001t0001g0068 a0001c0002t0002g0003 a0001c0002t0002g0004 others(136): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1771-69A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885300 | |||||||
chr14:104885313 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1771-56G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885313 | |||||||
chr14:104885336 | C | T | 116 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(113): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1771-33C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 9/18 | chr14 | 104885336 | |||||||
chr14:104885731 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1944+189T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/18 | chr14 | 104885731 | |||||||
chr14:104885781 | C | T | 9 | a0001c0014t0001g0018 a0001c0014t0001g0079 a0001c0070t0001g0158 others(6): Show |
10 | HG00733.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1944+239C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/18 | chr14 | 104885781 | |||||||
chr14:104885841 | G | A | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1945-199G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/18 | chr14 | 104885841 | |||||||
chr14:104885867 | T | C | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0091 others(5): Show |
9 | NA18952.hp2 NA18960.hp1 NA18975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1945-173T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/18 | chr14 | 104885867 | |||||||
chr14:104885918 | T | A | 137 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(134): Show |
162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1945-122T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 10/18 | chr14 | 104885918 | |||||||
chr14:104886196 | G | A | 1 | a0001c0003t0002g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2035+66G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 11/18 | chr14 | 104886196 | |||||||
chr14:104886199 | C | T | 12 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(9): Show |
13 | HG00438.hp1 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.2035+69C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 11/18 | chr14 | 104886199 | |||||||
chr14:104886246 | C | T | 3 | a0001c0005t0003g0038 a0001c0005t0003g0240 a0001c0005t0003g0241 |
4 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2036-29C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 11/18 | chr14 | 104886246 | |||||||
chr14:104888023 | C | G | 1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3739+45C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888023 | |||||||
chr14:104888138 | T | A | 1 | a0001c0001t0015g0048 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3739+160T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888138 | |||||||
chr14:104888151 | G | A | 1 | a0018c0079t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3739+173G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888151 | |||||||
chr14:104888161 | C | T | 20 | a0001c0017t0002g0162 a0001c0017t0002g0165 a0001c0017t0002g0166 others(17): Show |
20 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3739+183C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888161 | |||||||
chr14:104888208 | A | G | 138 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(135): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.3739+230A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888208 | |||||||
chr14:104888733 | A | C | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3739+755A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888733 | |||||||
chr14:104888735 | G | A | 24 | a0002c0004t0002g0002 a0002c0004t0002g0035 a0002c0004t0002g0036 others(21): Show |
33 | HG00408.hp2 HG00544.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.3739+757G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888735 | |||||||
chr14:104888848 | G | T | 13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.3740-772G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888848 | |||||||
chr14:104888964 | C | T | 1 | a0001c0010t0002g0060 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3740-656C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104888964 | |||||||
chr14:104889015 | A | T | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.3740-605A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889015 | |||||||
chr14:104889042 | C | T | 3 | a0001c0007t0008g0130 a0001c0007t0008g0131 a0001c0007t0008g0134 |
3 | HG02055.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3740-578C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889042 | |||||||
chr14:104889108 | T | A | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3740-512T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889108 | |||||||
chr14:104889212 | C | T | 116 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(113): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.3740-408C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889212 | |||||||
chr14:104889294 | C | T | 1 | a0028c0031t0001g0099 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3740-326C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889294 | |||||||
chr14:104889333 | TG | T | 37 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(34): Show |
39 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.3740-285delG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr14 | 104889333 | ||||||
chr14:104889455 | A | G | 1 | a0001c0005t0003g0238 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3740-165A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889455 | |||||||
chr14:104889582 | C | T | 1 | a0002c0009t0012g0175 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3740-38C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889582 | |||||||
chr14:104889617 | C | A | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | splice_region_variant&intron_variant | LOW | c.3740-3C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 12/18 | chr14 | 104889617 | |||||||
chr14:104889800 | G | C | 138 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(135): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.3878+42G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889800 | |||||||
chr14:104889834 | C | T | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3878+76C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889834 | |||||||
chr14:104889872 | C | T | 3 | a0001c0073t0002g0155 a0001c0075t0002g0154 a0032c0072t0002g0157 |
3 | HG02647.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3878+114C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889872 | |||||||
chr14:104889890 | CTGGATGG others(25): Show |
C | 2 | a0010c0086t0002g0206 a0025c0085t0002g0209 |
2 | NA18960.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.3878+145_3878+176d others(34): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889890 | ||||||
chr14:104889903 | CAAAT | C | 16 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 others(13): Show |
16 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.3878+146_3878+149d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889903 | |||||||
chr14:104889903 | CAAATGGA others(1): Show |
C | 16 | a0001c0006t0005g0028 a0001c0006t0007g0029 a0001c0020t0002g0031 others(13): Show |
17 | HG00438.hp1 HG01071.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.3878+146_3878+153d others(10): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889903 | |||||||
chr14:104889903 | CAAATGGA others(5): Show |
C | 77 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(74): Show |
96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.3878+146_3878+157d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889903 | |||||||
chr14:104889904 | A | G | 5 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(2): Show |
6 | HG01496.hp2 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.3878+146A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889904 | |||||||
chr14:104889905 | A | AATGG | 22 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0041 others(19): Show |
25 | HG00741.hp2 HG01346.hp1 HG01943.hp2 others(22): Show |
intron_variant | MODIFIER | c.3878+191_3878+194d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889905 | ||||||
chr14:104889905 | A | AATGGATG others(1): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0091 others(1): Show |
4 | HG01496.hp2 NA18952.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.3878+187_3878+194d others(10): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889905 | ||||||
chr14:104889905 | A | AATGGATG others(5): Show |
3 | a0001c0001t0001g0020 a0001c0001t0001g0051 a0001c0001t0001g0052 |
3 | HG01167.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3878+183_3878+194d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889905 | ||||||
chr14:104889905 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3878+147A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889905 | |||||||
chr14:104889905 | AATGG | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(20): Show |
27 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.3878+191_3878+194d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889905 | ||||||
chr14:104889909 | G | A | 16 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 others(13): Show |
16 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.3878+151G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889909 | |||||||
chr14:104889913 | G | A | 16 | a0001c0006t0005g0028 a0001c0006t0007g0029 a0001c0020t0002g0031 others(13): Show |
17 | HG00438.hp1 HG01071.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.3878+155G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889913 | |||||||
chr14:104889915 | T | G | 3 | a0001c0005t0003g0246 a0001c0008t0003g0253 a0001c0008t0003g0254 |
3 | HG02258.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3878+157T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889915 | |||||||
chr14:104889917 | G | A | 77 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(74): Show |
96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.3878+159G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889917 | |||||||
chr14:104889941 | GATGGATG others(5): Show |
G | 4 | a0001c0005t0003g0038 a0001c0005t0003g0240 a0001c0008t0003g0252 others(1): Show |
5 | HG02055.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.3878+195_3878+206d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889941 | ||||||
chr14:104889945 | GATGGATG others(1): Show |
G | 11 | a0001c0005t0003g0015 a0001c0005t0003g0246 a0001c0008t0003g0015 others(8): Show |
14 | HG01167.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.3878+195_3878+202d others(10): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889945 | ||||||
chr14:104889949 | G | GATGGATG others(9): Show |
1 | a0001c0001t0001g0095 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.3878+194_3878+195i others(18): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889949 | ||||||
chr14:104889949 | GATGA | G | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0005t0003g0238 others(2): Show |
5 | HG01255.hp1 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3878+195_3878+198d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889949 | ||||||
chr14:104889951 | TGAATGGA others(4): Show |
T | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3878+194_3878+204d others(13): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889951 | |||||||
chr14:104889953 | A | G | 11 | a0001c0001t0001g0128 a0001c0005t0003g0242 a0001c0005t0003g0243 others(8): Show |
12 | HG00733.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3878+195A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889953 | |||||||
chr14:104889957 | G | A | 7 | a0001c0014t0001g0018 a0001c0014t0001g0079 a0004c0021t0006g0232 others(4): Show |
8 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3878+199G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889957 | |||||||
chr14:104889963 | T | A | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3878+205T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889963 | |||||||
chr14:104889966 | A | C | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+208A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889966 | |||||||
chr14:104889968 | A | G | 8 | a0001c0014t0001g0018 a0001c0014t0001g0079 a0004c0021t0006g0232 others(5): Show |
9 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3878+210A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889968 | |||||||
chr14:104889969 | G | GA | 7 | a0001c0014t0001g0018 a0001c0014t0001g0079 a0004c0021t0006g0232 others(4): Show |
8 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3878+211_3878+212i others(3): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889969 | |||||||
chr14:104889970 | G | T | 7 | a0001c0014t0001g0018 a0001c0014t0001g0079 a0004c0021t0006g0232 others(4): Show |
8 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3878+212G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889970 | |||||||
chr14:104889971 | A | AGGGT | 114 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(111): Show |
135 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.3878+224_3878+227d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104889971 | ||||||
chr14:104889971 | A | T | 1 | a0022c0068t0020g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3878+213A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889971 | |||||||
chr14:104889986 | A | G | 2 | a0001c0001t0001g0054 a0001c0015t0001g0066 |
2 | HG01346.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3878+228A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104889986 | |||||||
chr14:104890044 | A | G | 138 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(135): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.3878+286A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890044 | |||||||
chr14:104890103 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3878+345T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890103 | |||||||
chr14:104890136 | G | T | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+378G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890136 | |||||||
chr14:104890161 | CATGGATG others(5): Show |
C | 20 | a0001c0017t0002g0162 a0001c0017t0002g0165 a0001c0017t0002g0166 others(17): Show |
20 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3878+420_3878+431d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890161 | ||||||
chr14:104890186 | A | G | 2 | a0001c0065t0002g0255 a0009c0025t0002g0039 |
3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3878+428A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890186 | |||||||
chr14:104890214 | A | G | 19 | a0001c0017t0002g0162 a0001c0017t0002g0165 a0001c0017t0002g0166 others(16): Show |
19 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.3878+456A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890214 | |||||||
chr14:104890346 | G | GTGGA | 22 | a0001c0005t0003g0015 a0001c0005t0003g0038 a0001c0005t0003g0238 others(19): Show |
26 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.3878+603_3878+606d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890346 | ||||||
chr14:104890354 | A | T | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+596A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890354 | |||||||
chr14:104890358 | A | ATGGAT | 116 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(113): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.3878+601_3878+605d others(7): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890358 | ||||||
chr14:104890373 | G | C | 13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.3878+615G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890373 | |||||||
chr14:104890390 | G | GTGGA | 4 | a0001c0054t0001g0081 a0010c0086t0002g0206 a0021c0052t0001g0055 others(1): Show |
4 | HG02809.hp2 HG02922.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.3878+659_3878+662d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890390 | ||||||
chr14:104890390 | G | GTGGATGG others(5): Show |
10 | a0001c0014t0001g0079 a0001c0058t0001g0077 a0001c0059t0001g0078 others(7): Show |
10 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.3878+651_3878+662d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890390 | ||||||
chr14:104890390 | G | GTGGATGG others(9): Show |
1 | a0001c0070t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3878+647_3878+662d others(18): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890390 | ||||||
chr14:104890390 | G | GTGGATGG others(109): Show |
1 | a0001c0014t0001g0018 | 2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3878+662_3878+663i others(118): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890390 | ||||||
chr14:104890390 | GTGGA | G | 14 | a0001c0001t0001g0020 a0001c0001t0001g0107 a0001c0001t0023g0090 others(11): Show |
18 | HG01074.hp2 HG01256.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.3878+659_3878+662d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890390 | ||||||
chr14:104890421 | A | G | 2 | a0001c0054t0001g0081 a0021c0052t0001g0055 |
2 | HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3878+663A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890421 | |||||||
chr14:104890531 | T | C | 1 | a0001c0007t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3878+773T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890531 | |||||||
chr14:104890566 | G | GTGGA | 113 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(110): Show |
133 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.3878+828_3878+831d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890566 | ||||||
chr14:104890566 | G | GTGGATGG others(5): Show |
19 | a0001c0005t0003g0015 a0001c0005t0003g0038 a0001c0005t0003g0238 others(16): Show |
23 | HG01167.hp2 HG01255.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.3878+820_3878+831d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890566 | ||||||
chr14:104890566 | G | GTGGATGG others(9): Show |
1 | a0008c0027t0003g0249 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3878+816_3878+831d others(18): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890566 | ||||||
chr14:104890590 | G | A | 14 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(11): Show |
15 | HG00280.hp1 HG00438.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3878+832G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890590 | |||||||
chr14:104890593 | A | G | 14 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(11): Show |
15 | HG00280.hp1 HG00438.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3878+835A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890593 | |||||||
chr14:104890662 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3878+904G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890662 | |||||||
chr14:104890698 | G | GTGGATGG others(5): Show |
1 | a0001c0035t0013g0150 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3878+947_3878+958d others(14): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890698 | ||||||
chr14:104890719 | T | TG | 23 | a0001c0005t0003g0015 a0001c0005t0003g0038 a0001c0005t0003g0238 others(20): Show |
27 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.3878+963dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | ||||||
chr14:104890719 | T | TGGGTGGG others(34): Show |
1 | a0001c0010t0002g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3878+963_3878+964i others(43): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | ||||||
chr14:104890719 | T | TGGGTGGG others(33): Show |
1 | a0025c0085t0002g0209 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3878+963_3878+964i others(42): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | ||||||
chr14:104890719 | T | TGGGTGGG others(34): Show |
107 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(104): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.3878+963_3878+964i others(43): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | ||||||
chr14:104890719 | T | TGGGTGGG others(74): Show |
3 | a0001c0062t0002g0169 a0001c0065t0002g0255 a0009c0025t0002g0039 |
4 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3878+963_3878+964i others(83): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | ||||||
chr14:104890719 | T | TGGGTGGG others(78): Show |
1 | a0001c0061t0017g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3878+963_3878+964i others(87): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | ||||||
chr14:104890719 | T | TGGGTGGG others(34): Show |
2 | a0001c0017t0002g0165 a0001c0017t0002g0166 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3878+963_3878+964i others(43): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890719 | ||||||
chr14:104890738 | T | A | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+980T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890738 | |||||||
chr14:104890740 | GATGA | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0132 |
3 | HG00639.hp1 HG01175.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.3878+986_3878+989d others(6): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890740 | ||||||
chr14:104890829 | A | T | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+1071A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890829 | |||||||
chr14:104890848 | A | AATGAGTG others(25): Show |
1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3878+1107_3878+113 others(36): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890848 | ||||||
chr14:104890897 | A | G | 2 | a0001c0061t0017g0170 a0001c0062t0002g0169 |
2 | HG01496.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3878+1139A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890897 | |||||||
chr14:104890972 | G | GGTGT | 4 | a0001c0007t0001g0111 a0005c0016t0001g0025 a0005c0016t0014g0088 others(1): Show |
5 | HG02572.hp1 HG03486.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3878+1218_3878+122 others(8): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104890972 | ||||||
chr14:104890989 | G | A | 116 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(113): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.3878+1231G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104890989 | |||||||
chr14:104891014 | A | T | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+1256A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891014 | |||||||
chr14:104891048 | T | A | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1290T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891048 | |||||||
chr14:104891050 | A | T | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1292A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891050 | |||||||
chr14:104891052 | T | A | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1294T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891052 | |||||||
chr14:104891053 | G | T | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1295G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891053 | |||||||
chr14:104891058 | G | C | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1300G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891058 | |||||||
chr14:104891068 | TGGATGGA others(29): Show |
T | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1313_3878+134 others(40): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104891068 | ||||||
chr14:104891110 | G | A | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1352G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891110 | |||||||
chr14:104891124 | T | G | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1366T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891124 | |||||||
chr14:104891126 | C | T | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1368C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891126 | |||||||
chr14:104891139 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3878+1381C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891139 | |||||||
chr14:104891146 | T | A | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1388T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891146 | |||||||
chr14:104891147 | A | T | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1389A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891147 | |||||||
chr14:104891149 | A | C | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1391A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891149 | |||||||
chr14:104891150 | A | C | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1392A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891150 | |||||||
chr14:104891153 | A | C | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1395A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891153 | |||||||
chr14:104891154 | G | A | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1396G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891154 | |||||||
chr14:104891169 | T | G | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1411T>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891169 | |||||||
chr14:104891171 | T | A | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+1413T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891171 | |||||||
chr14:104891181 | A | C | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1423A>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891181 | |||||||
chr14:104891182 | T | A | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1424T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891182 | |||||||
chr14:104891248 | T | A | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3878+1490T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891248 | |||||||
chr14:104891269 | G | C | 1 | a0001c0001t0001g0041 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3878+1511G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891269 | |||||||
chr14:104891299 | T | A | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3878+1541T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891299 | |||||||
chr14:104891325 | G | C | 2 | a0001c0001t0001g0083 a0001c0055t0001g0084 |
2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3878+1567G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891325 | |||||||
chr14:104891326 | G | T | 2 | a0001c0001t0001g0083 a0001c0055t0001g0084 |
2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3878+1568G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891326 | |||||||
chr14:104891328 | G | A | 2 | a0001c0001t0001g0083 a0001c0055t0001g0084 |
2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3878+1570G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891328 | |||||||
chr14:104891329 | C | A | 2 | a0001c0001t0001g0083 a0001c0055t0001g0084 |
2 | NA18969.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.3878+1571C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891329 | |||||||
chr14:104891332 | G | T | 1 | a0001c0070t0001g0158 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3878+1574G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891332 | |||||||
chr14:104891334 | A | AG | 11 | a0001c0001t0001g0091 a0001c0001t0001g0109 a0001c0001t0001g0118 others(8): Show |
12 | HG00544.hp1 HG00642.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.3878+1583dupG | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104891334 | ||||||
chr14:104891432 | G | GGGAGGCC others(56): Show |
1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3879-1543_3879-154 others(67): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104891432 | ||||||
chr14:104891434 | C | T | 17 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(14): Show |
19 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.3879-1542C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891434 | |||||||
chr14:104891435 | G | A | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3879-1541G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891435 | |||||||
chr14:104891437 | C | G | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3879-1539C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891437 | |||||||
chr14:104891439 | C | A | 1 | a0002c0004t0002g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3879-1537C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891439 | |||||||
chr14:104891695 | G | A | 79 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(76): Show |
98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.3879-1281G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891695 | |||||||
chr14:104891777 | A | T | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3879-1199A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891777 | |||||||
chr14:104891797 | G | C | 1 | a0001c0010t0002g0058 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3879-1179G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891797 | |||||||
chr14:104891798 | C | G | 1 | a0001c0010t0002g0058 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3879-1178C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891798 | |||||||
chr14:104891839 | C | T | 1 | a0001c0003t0022g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3879-1137C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891839 | |||||||
chr14:104891978 | T | C | 116 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(113): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.3879-998T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891978 | |||||||
chr14:104891983 | G | A | 2 | a0014c0045t0001g0137 a0018c0079t0001g0040 |
2 | HG00733.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.3879-993G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891983 | |||||||
chr14:104891993 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3879-983C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891993 | |||||||
chr14:104891994 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3879-982T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104891994 | |||||||
chr14:104892012 | C | T | 116 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0032 others(113): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.3879-964C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892012 | |||||||
chr14:104892175 | G | T | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3879-801G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892175 | |||||||
chr14:104892188 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3879-788T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892188 | |||||||
chr14:104892224 | A | G | 1 | a0001c0019t0002g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3879-752A>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892224 | |||||||
chr14:104892227 | TGACGAGG others(6): Show |
T | 1 | a0001c0001t0001g0070 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3879-747_3879-735d others(15): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104892227 | ||||||
chr14:104892230 | C | T | 1 | a0001c0005t0003g0242 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3879-746C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892230 | |||||||
chr14:104892251 | A | T | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3879-725A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892251 | |||||||
chr14:104892275 | C | T | 21 | a0001c0005t0003g0015 a0001c0005t0003g0038 a0001c0005t0003g0238 others(18): Show |
25 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.3879-701C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892275 | |||||||
chr14:104892292 | C | T | 20 | a0001c0017t0002g0162 a0001c0017t0002g0165 a0001c0017t0002g0166 others(17): Show |
20 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3879-684C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892292 | |||||||
chr14:104892306 | T | A | 1 | a0007c0024t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3879-670T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892306 | |||||||
chr14:104892322 | T | C | 22 | a0001c0005t0003g0015 a0001c0005t0003g0038 a0001c0005t0003g0238 others(19): Show |
26 | HG01167.hp2 HG01255.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.3879-654T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892322 | |||||||
chr14:104892391 | T | A | 1 | a0001c0001t0001g0041 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3879-585T>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892391 | |||||||
chr14:104892441 | ATCTGCCC others(10): Show |
A | 20 | a0001c0006t0005g0043 a0001c0006t0005g0076 a0001c0006t0005g0146 others(17): Show |
22 | HG00733.hp1 HG01099.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.3879-504_3879-488d others(19): Show |
CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr14 | 104892441 | ||||||
chr14:104892547 | C | T | 1 | a0001c0002t0002g0221 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3879-429C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892547 | |||||||
chr14:104892662 | C | G | 2 | a0001c0065t0002g0255 a0009c0025t0002g0039 |
3 | HG03195.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3879-314C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892662 | |||||||
chr14:104892670 | G | T | 1 | a0001c0003t0002g0208 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3879-306G>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892670 | |||||||
chr14:104892706 | T | C | 1 | a0027c0044t0001g0122 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3879-270T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892706 | |||||||
chr14:104892740 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3879-236C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892740 | |||||||
chr14:104892956 | G | A | 9 | a0001c0014t0001g0018 a0001c0014t0001g0079 a0001c0070t0001g0158 others(6): Show |
10 | HG00733.hp1 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3879-20G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892956 | |||||||
chr14:104892968 | G | A | 13 | a0001c0006t0005g0028 a0001c0006t0005g0043 a0001c0006t0005g0076 others(10): Show |
14 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.3879-8G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892968 | |||||||
chr14:104892969 | G | C | 117 | a0001c0001t0002g0230 a0001c0002t0002g0003 a0001c0002t0002g0004 others(114): Show |
138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
splice_region_variant&intron_variant | LOW | c.3879-7G>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892969 | |||||||
chr14:104892970 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18982.hp1 | splice_region_variant&intron_variant | LOW | c.3879-6C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 13/18 | chr14 | 104892970 | |||||||
chr14:104893179 | C | T | 1 | a0009c0025t0002g0039 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4038+44C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893179 | |||||||
chr14:104893180 | G | A | 1 | a0001c0053t0001g0085 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4038+45G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893180 | |||||||
chr14:104893211 | T | C | 1 | a0001c0015t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4038+76T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893211 | |||||||
chr14:104893219 | C | T | 1 | a0001c0037t0005g0149 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4038+84C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893219 | |||||||
chr14:104893297 | C | T | 1 | a0001c0011t0001g0126 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4038+162C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893297 | |||||||
chr14:104893306 | C | G | 1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4038+171C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893306 | |||||||
chr14:104893322 | C | T | 117 | a0001c0001t0002g0230 a0001c0002t0002g0003 a0001c0002t0002g0004 others(114): Show |
138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.4038+187C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893322 | |||||||
chr14:104893413 | C | T | 1 | a0001c0002t0002g0034 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4039-110C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893413 | |||||||
chr14:104893490 | T | C | 152 | a0001c0001t0002g0230 a0001c0002t0002g0003 a0001c0002t0002g0004 others(149): Show |
178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.4039-33T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 14/18 | chr14 | 104893490 | |||||||
chr14:104893941 | G | A | 1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4271+92G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104893941 | |||||||
chr14:104893954 | C | G | 1 | a0001c0019t0002g0160 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4271+105C>G | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104893954 | |||||||
chr14:104893956 | C | T | 4 | a0001c0061t0017g0170 a0001c0062t0002g0169 a0001c0065t0002g0255 others(1): Show |
5 | HG01496.hp2 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4271+107C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104893956 | |||||||
chr14:104893964 | C | T | 1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4271+115C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104893964 | |||||||
chr14:104893991 | G | A | 1 | a0001c0008t0003g0247 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4271+142G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104893991 | |||||||
chr14:104894018 | C | T | 79 | a0001c0001t0002g0230 a0001c0002t0002g0003 a0001c0002t0002g0004 others(76): Show |
98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.4271+169C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104894018 | |||||||
chr14:104894026 | A | T | 1 | a0002c0064t0002g0163 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4271+177A>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104894026 | |||||||
chr14:104894164 | C | T | 1 | a0001c0010t0002g0058 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4272-121C>T | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104894164 | |||||||
chr14:104894228 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4272-57C>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 16/18 | chr14 | 104894228 | |||||||
chr14:104894385 | G | A | 1 | a0020c0040t0011g0258 | 1 | HG02723.hp1 | splice_region_variant&intron_variant | LOW | c.4365+7G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 17/18 | chr14 | 104894385 | |||||||
chr14:104894409 | T | C | 152 | a0001c0001t0001g0062 a0001c0001t0002g0230 a0001c0002t0002g0003 others(149): Show |
178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.4365+31T>C | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 17/18 | chr14 | 104894409 | |||||||
chr14:104894610 | G | A | 1 | a0001c0003t0021g0231 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4417+22G>A | CEP170B | ENSG00000099814.17 | transcript | ENST00000414716.8 | protein_coding | 18/18 | chr14 | 104894610 |