Item | Value |
---|---|
geneid | 22994 |
ensemblid | ENSG00000141577.14 |
hgncid | 29511 |
symbol | CEP131 |
name | centrosomal protein 131 |
refseq_nuc | NM_014984.4 |
refseq_prot | NP_055799.2 |
ensembl_nuc | ENST00000450824.7 |
ensembl_prot | ENSP00000393583.2 |
mane_status | MANE Select |
chr | chr17 |
start | 81189596 |
end | 81222965 |
strand | - |
ver | v1.2 |
region | chr17:81189596-81222965 |
region5000 | chr17:81184596-81227965 |
regionname0 | CEP131_chr17_81189596_81222965 |
regionname5000 | CEP131_chr17_81184596_81227965 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1080 | 197 | 27 | 44 | 83 | 13 | 29 | 58 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0002 | 0/0 | 1080 | 51 | 16 | 2 | 26 | 1 | 6 | 20 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0003 | 0/0 | 1080 | 18 | 18 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0004 | 0/0 | 1080 | 13 | 3 | 1 | 9 | 0 | 0 | 6 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0005 | 0/0 | 1080 | 10 | 0 | 0 | 10 | 0 | 0 | 10 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0006 | 0/0 | 1080 | 9 | 0 | 7 | 2 | 0 | 0 | 2 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0007 | 1/0 | 1080 | 8 | 5 | 2 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0008 | 0/0 | 1080 | 9 | 2 | 0 | 6 | 0 | 1 | 6 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0009 | 0/0 | 1080 | 5 | 0 | 2 | 0 | 2 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0010 | 0/0 | 1080 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0011 | 0/0 | 1080 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0012 | 0/0 | 1080 | 4 | 0 | 1 | 3 | 0 | 0 | 3 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0013 | 0/0 | 1080 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0014 | 0/0 | 1080 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0015 | 0/0 | 1080 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0016 | 0/0 | 1080 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0017 | 0/0 | 1080 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0018 | 0/0 | 1080 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0019 | 0/0 | 1080 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0020 | 0/0 | 1080 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0021 | 0/0 | 1080 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0022 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0023 | 0/0 | 1080 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0024 | 0/0 | 1080 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0025 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0026 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0027 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0028 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0029 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0030 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0031 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0032 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0033 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0034 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0035 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0036 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0037 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0038 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0039 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0040 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0041 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0042 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0043 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0044 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0045 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0046 | 0/0 | 1080 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0047 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
a0048 | 0/0 | 1080 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | MKGTR others(1075): Show |
chr17 | 81184596 | 81227965 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3240 | 97 | 3 | 14 | 58 | 2 | 19 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0001c0003 | 0/0 | 3240 | 49 | 16 | 22 | 1 | 6 | 4 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0001c0004 | 0/0 | 3240 | 31 | 5 | 4 | 17 | 2 | 3 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0001c0012 | 0/0 | 3240 | 5 | 0 | 0 | 0 | 3 | 2 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0001c0018 | 0/0 | 3240 | 4 | 0 | 0 | 4 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0001c0019 | 0/0 | 3240 | 4 | 0 | 4 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0001c0027 | 0/0 | 3240 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0001c0051 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0001c0054 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0001c0058 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0001c0062 | 0/0 | 3240 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0001c0074 | 0/0 | 3240 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0002c0002 | 0/0 | 3240 | 49 | 15 | 2 | 26 | 1 | 5 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0002c0047 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0002c0061 | 0/0 | 3240 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0003c0008 | 0/0 | 3240 | 8 | 8 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0003c0014 | 0/0 | 3240 | 4 | 4 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0003c0020 | 0/0 | 3240 | 3 | 3 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0003c0023 | 0/0 | 3240 | 2 | 2 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0003c0031 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0004c0005 | 0/0 | 3240 | 11 | 2 | 0 | 9 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0004c0044 | 0/0 | 3240 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0004c0045 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0005c0006 | 0/0 | 3240 | 10 | 0 | 0 | 10 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0006c0007 | 0/0 | 3240 | 9 | 0 | 7 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0007c0009 | 1/0 | 3240 | 8 | 5 | 2 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0008c0010 | 0/0 | 3240 | 6 | 0 | 0 | 5 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0008c0050 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0008c0052 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0008c0064 | 0/0 | 3240 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0009c0011 | 0/0 | 3240 | 5 | 0 | 2 | 0 | 2 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0010c0013 | 0/0 | 3240 | 5 | 0 | 0 | 0 | 0 | 5 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0011c0015 | 0/0 | 3240 | 4 | 2 | 2 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0012c0016 | 0/0 | 3240 | 4 | 0 | 1 | 3 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0013c0017 | 0/0 | 3240 | 4 | 0 | 0 | 4 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0014c0021 | 0/0 | 3240 | 3 | 0 | 2 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0015c0022 | 0/0 | 3240 | 3 | 3 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0016c0038 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0016c0040 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0016c0042 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0017c0024 | 0/0 | 3240 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0017c0037 | 0/0 | 3240 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0018c0028 | 0/0 | 3240 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0019c0025 | 0/0 | 3240 | 2 | 0 | 1 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0020c0056 | 0/0 | 3240 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0020c0066 | 0/0 | 3240 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0021c0026 | 0/0 | 3240 | 2 | 2 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0022c0063 | 0/0 | 3240 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0023c0049 | 0/0 | 3240 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0024c0035 | 0/0 | 3240 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0025c0071 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0026c0072 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0027c0053 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0028c0073 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0029c0067 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0030c0059 | 0/0 | 3240 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0031c0070 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0032c0043 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0033c0068 | 0/0 | 3240 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0034c0032 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0035c0048 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0036c0057 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0037c0041 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0038c0055 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0039c0029 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0040c0033 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0041c0030 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0042c0065 | 0/0 | 3240 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0043c0039 | 0/0 | 3240 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0044c0046 | 0/0 | 3240 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0045c0036 | 0/0 | 3240 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0046c0060 | 0/0 | 3240 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0047c0069 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 | ||
a0048c0034 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | ATGAA others(3235): Show |
chr17 | 81184596 | 81227965 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3630 | 97 | 3 | 14 | 58 | 2 | 19 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0003t0001 | 0/0 | 3630 | 2 | 1 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0003t0002 | 0/0 | 3630 | 41 | 15 | 20 | 1 | 2 | 3 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0003t0005 | 0/0 | 3630 | 5 | 0 | 1 | 0 | 3 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0003t0010 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0004t0001 | 0/0 | 3630 | 18 | 2 | 1 | 11 | 1 | 3 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0004t0002 | 0/0 | 3630 | 13 | 3 | 3 | 6 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0012t0001 | 0/0 | 3630 | 5 | 0 | 0 | 0 | 3 | 2 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0018t0001 | 0/0 | 3630 | 4 | 0 | 0 | 4 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0019t0001 | 0/0 | 3630 | 4 | 0 | 4 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0027t0001 | 0/0 | 3630 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0051t0002 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0054t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0058t0003 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0062t0001 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0001c0074t0001 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0002c0002t0001 | 0/0 | 3630 | 3 | 2 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0002c0002t0002 | 0/0 | 3630 | 45 | 12 | 2 | 25 | 1 | 5 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0002c0002t0012 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0002c0047t0002 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0002c0061t0001 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0003c0008t0003 | 0/0 | 3630 | 8 | 8 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0003c0014t0003 | 0/0 | 3630 | 4 | 4 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0003c0020t0003 | 0/0 | 3630 | 3 | 3 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0003c0023t0003 | 0/0 | 3630 | 2 | 2 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0003c0031t0007 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0004c0005t0001 | 0/0 | 3630 | 11 | 2 | 0 | 9 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0004c0044t0011 | 0/0 | 3630 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0004c0045t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0005c0006t0001 | 0/0 | 3630 | 10 | 0 | 0 | 10 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0006c0007t0001 | 0/0 | 3630 | 9 | 0 | 7 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0007c0009t0001 | 1/0 | 3630 | 8 | 5 | 2 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0008c0010t0001 | 0/0 | 3630 | 4 | 0 | 0 | 3 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0008c0010t0002 | 0/0 | 3630 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0008c0050t0002 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0008c0052t0002 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0008c0064t0001 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0009c0011t0001 | 0/0 | 3630 | 5 | 0 | 2 | 0 | 2 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0010c0013t0004 | 0/0 | 3630 | 5 | 0 | 0 | 0 | 0 | 5 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0011c0015t0006 | 0/0 | 3630 | 4 | 2 | 2 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0012c0016t0001 | 0/0 | 3630 | 4 | 0 | 1 | 3 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0013c0017t0001 | 0/0 | 3630 | 4 | 0 | 0 | 4 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0014c0021t0002 | 0/0 | 3630 | 3 | 0 | 2 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0015c0022t0001 | 0/0 | 3630 | 3 | 3 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0016c0038t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0016c0040t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0016c0042t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0017c0024t0001 | 0/0 | 3630 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0017c0037t0001 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0018c0028t0001 | 0/0 | 3630 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0019c0025t0002 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0019c0025t0008 | 0/0 | 3630 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0020c0056t0001 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0020c0066t0001 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0021c0026t0003 | 0/0 | 3630 | 2 | 2 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0022c0063t0001 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0023c0049t0002 | 0/0 | 3630 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0024c0035t0003 | 0/0 | 3630 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0025c0071t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0026c0072t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0027c0053t0002 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0028c0073t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0029c0067t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0030c0059t0001 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0031c0070t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0032c0043t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0033c0068t0004 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0034c0032t0003 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0035c0048t0002 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0036c0057t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0037c0041t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0038c0055t0009 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0039c0029t0001 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0040c0033t0003 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0041c0030t0003 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0042c0065t0001 | 0/0 | 3630 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0043c0039t0001 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0044c0046t0002 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0045c0036t0001 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0046c0060t0001 | 0/0 | 3630 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0047c0069t0002 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
a0048c0034t0003 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | AGCTG others(3625): Show |
chr17 | 81184596 | 81227965 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0005g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0003t0010g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0004t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0012t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0012t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0012t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0012t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0012t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0018t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0018t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0018t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0018t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0019t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0019t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0019t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0019t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0027t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0027t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0051t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0054t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0058t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0062t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0001c0074t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0001 | 0/0 | 8 | 0 | 0 | 7 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0002t0012g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0047t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0002c0061t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0008t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0008t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0008t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0008t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0008t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0008t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0008t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0008t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0014t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0014t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0014t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0014t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0020t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0020t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0023t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0023t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0003c0031t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0005t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0005t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0005t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0005t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0005t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0005t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0005t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0005t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0005t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0005t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0044t0011g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0004c0045t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0005c0006t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0005c0006t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0005c0006t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0005c0006t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0005c0006t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0005c0006t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0006c0007t0001g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0006c0007t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0006c0007t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0006c0007t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0006c0007t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0007c0009t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0007c0009t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0007c0009t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0007c0009t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0007c0009t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0007c0009t0001g0266 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0007c0009t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0007c0009t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0008c0010t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0008c0010t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0008c0010t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0008c0010t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0008c0010t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0008c0010t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0008c0050t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0008c0052t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0008c0064t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0009c0011t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0009c0011t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0009c0011t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0009c0011t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0010c0013t0004g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0010c0013t0004g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0010c0013t0004g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0010c0013t0004g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0010c0013t0004g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0011c0015t0006g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0011c0015t0006g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0011c0015t0006g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0011c0015t0006g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0012c0016t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0012c0016t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0012c0016t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0012c0016t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0013c0017t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0013c0017t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0013c0017t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0013c0017t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0014c0021t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0014c0021t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0014c0021t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0015c0022t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0015c0022t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0015c0022t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0016c0038t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0016c0040t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0016c0042t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0017c0024t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0017c0024t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0017c0037t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0018c0028t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0018c0028t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0019c0025t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0019c0025t0008g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0020c0056t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0020c0066t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0021c0026t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0021c0026t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0022c0063t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0023c0049t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0024c0035t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0025c0071t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0026c0072t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0027c0053t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0028c0073t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0029c0067t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0030c0059t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0031c0070t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0032c0043t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0033c0068t0004g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0034c0032t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0035c0048t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0036c0057t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0037c0041t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0038c0055t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0039c0029t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0040c0033t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0041c0030t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0042c0065t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0043c0039t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0044c0046t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0045c0036t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0046c0060t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0047c0069t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
a0048c0034t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0005 | g0125 | EUR | GBR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00099 | hp2 | a0001 | c0004 | t0001 | g0289 | EUR | GBR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00140 | hp1 | a0009 | c0011 | t0001 | g0224 | EUR | GBR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | GBR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00280 | hp1 | a0022 | c0063 | t0001 | g0184 | EUR | FIN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00280 | hp2 | a0001 | c0012 | t0001 | g0143 | EUR | FIN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | FIN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00323 | hp2 | a0001 | c0003 | t0002 | g0076 | EUR | FIN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00423 | hp1 | a0018 | c0028 | t0001 | g0221 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00438 | hp1 | a0004 | c0005 | t0001 | g0274 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00621 | hp1 | a0004 | c0005 | t0001 | g0277 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0087 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00642 | hp1 | a0001 | c0003 | t0002 | g0108 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00642 | hp2 | a0009 | c0011 | t0001 | g0018 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00673 | hp2 | a0001 | c0004 | t0001 | g0298 | EAS | CHS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00733 | hp1 | a0001 | c0003 | t0002 | g0083 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00733 | hp2 | a0001 | c0003 | t0005 | g0122 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00735 | hp2 | a0001 | c0003 | t0002 | g0085 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG00741 | hp2 | a0001 | c0019 | t0001 | g0208 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01070 | hp1 | a0014 | c0021 | t0002 | g0063 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01070 | hp2 | a0006 | c0007 | t0001 | g0002 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01071 | hp1 | a0006 | c0007 | t0001 | g0002 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01074 | hp1 | a0023 | c0049 | t0002 | g0090 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01074 | hp2 | a0007 | c0009 | t0001 | g0265 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01081 | hp1 | a0001 | c0003 | t0002 | g0007 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01081 | hp2 | a0001 | c0003 | t0002 | g0048 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01106 | hp1 | a0019 | c0025 | t0008 | g0077 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01106 | hp2 | a0006 | c0007 | t0001 | g0002 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0065 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01167 | hp1 | a0001 | c0003 | t0002 | g0029 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01167 | hp2 | a0011 | c0015 | t0006 | g0321 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01168 | hp1 | a0001 | c0003 | t0002 | g0088 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01169 | hp1 | a0001 | c0003 | t0002 | g0059 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01169 | hp2 | a0011 | c0015 | t0006 | g0323 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01192 | hp2 | a0009 | c0011 | t0001 | g0018 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01243 | hp1 | a0001 | c0003 | t0002 | g0006 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01243 | hp2 | a0001 | c0003 | t0002 | g0105 | AMR | PUR | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01255 | hp1 | a0014 | c0021 | t0002 | g0079 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01255 | hp2 | a0024 | c0035 | t0003 | g0312 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01256 | hp1 | a0007 | c0009 | t0001 | g0279 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01256 | hp2 | a0001 | c0003 | t0002 | g0012 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01257 | hp2 | a0001 | c0004 | t0002 | g0030 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01258 | hp1 | a0001 | c0003 | t0002 | g0012 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01258 | hp2 | a0001 | c0004 | t0002 | g0011 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01261 | hp1 | a0001 | c0003 | t0002 | g0066 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01261 | hp2 | a0001 | c0003 | t0002 | g0081 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0028 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01358 | hp1 | a0004 | c0044 | t0011 | g0297 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01358 | hp2 | a0012 | c0016 | t0001 | g0251 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01496 | hp1 | a0001 | c0004 | t0001 | g0290 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01496 | hp2 | a0001 | c0003 | t0002 | g0007 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01515 | hp2 | a0001 | c0012 | t0001 | g0147 | EUR | IBS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01516 | hp1 | a0001 | c0003 | t0005 | g0121 | EUR | IBS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0064 | EUR | IBS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01517 | hp1 | a0001 | c0003 | t0005 | g0124 | EUR | IBS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01517 | hp2 | a0001 | c0012 | t0001 | g0146 | EUR | IBS | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01884 | hp1 | a0003 | c0008 | t0003 | g0310 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01884 | hp2 | a0011 | c0015 | t0006 | g0320 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01891 | hp1 | a0025 | c0071 | t0001 | g0128 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01891 | hp2 | a0026 | c0072 | t0001 | g0303 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01928 | hp2 | a0006 | c0007 | t0001 | g0216 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01934 | hp1 | a0001 | c0019 | t0001 | g0171 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01934 | hp2 | a0001 | c0003 | t0002 | g0049 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01943 | hp1 | a0006 | c0007 | t0001 | g0002 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0293 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01975 | hp1 | a0006 | c0007 | t0001 | g0002 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01975 | hp2 | a0001 | c0019 | t0001 | g0189 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01981 | hp2 | a0001 | c0019 | t0001 | g0229 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01993 | hp2 | a0001 | c0003 | t0002 | g0037 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02015 | hp1 | a0001 | c0004 | t0001 | g0282 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02055 | hp1 | a0001 | c0004 | t0002 | g0051 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02055 | hp2 | a0003 | c0023 | t0003 | g0327 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02071 | hp2 | a0001 | c0003 | t0002 | g0118 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02074 | hp1 | a0001 | c0074 | t0001 | g0241 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02074 | hp2 | a0001 | c0004 | t0002 | g0102 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02080 | hp1 | a0020 | c0066 | t0001 | g0213 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02129 | hp2 | a0020 | c0056 | t0001 | g0148 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02132 | hp2 | a0013 | c0017 | t0001 | g0200 | EAS | KHV | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02145 | hp1 | a0004 | c0005 | t0001 | g0296 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02145 | hp2 | a0001 | c0058 | t0003 | g0331 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02257 | hp1 | a0027 | c0053 | t0002 | g0032 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02258 | hp1 | a0002 | c0002 | t0002 | g0104 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02258 | hp2 | a0015 | c0022 | t0001 | g0129 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02273 | hp1 | a0001 | c0004 | t0002 | g0045 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02273 | hp2 | a0006 | c0007 | t0001 | g0174 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0062 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02280 | hp2 | a0003 | c0014 | t0003 | g0324 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02451 | hp1 | a0002 | c0047 | t0002 | g0034 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02451 | hp2 | a0003 | c0008 | t0003 | g0317 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02572 | hp1 | a0029 | c0067 | t0001 | g0126 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02602 | hp1 | a0030 | c0059 | t0001 | g0163 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02602 | hp2 | a0001 | c0004 | t0001 | g0149 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02615 | hp1 | a0003 | c0014 | t0003 | g0314 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02615 | hp2 | a0031 | c0070 | t0001 | g0127 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0052 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02622 | hp2 | a0003 | c0014 | t0003 | g0325 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02630 | hp1 | a0032 | c0043 | t0001 | g0246 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02630 | hp2 | a0003 | c0008 | t0003 | g0328 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02647 | hp2 | a0002 | c0002 | t0012 | g0304 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0046 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0114 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0056 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02717 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02723 | hp1 | a0015 | c0022 | t0001 | g0131 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02723 | hp2 | a0001 | c0003 | t0002 | g0061 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02735 | hp2 | a0033 | c0068 | t0004 | g0332 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02738 | hp1 | a0001 | c0003 | t0002 | g0007 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0074 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02809 | hp2 | a0002 | c0002 | t0002 | g0117 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0072 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02818 | hp2 | a0034 | c0032 | t0003 | g0315 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02886 | hp1 | a0007 | c0009 | t0001 | g0259 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0120 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02895 | hp1 | a0001 | c0003 | t0002 | g0073 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02895 | hp2 | a0016 | c0042 | t0001 | g0245 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02896 | hp2 | a0003 | c0008 | t0003 | g0307 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02897 | hp2 | a0001 | c0003 | t0002 | g0071 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02922 | hp1 | a0003 | c0008 | t0003 | g0308 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02922 | hp2 | a0035 | c0048 | t0002 | g0031 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02965 | hp1 | a0036 | c0057 | t0001 | g0138 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02965 | hp2 | a0001 | c0004 | t0002 | g0075 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02970 | hp1 | a0015 | c0022 | t0001 | g0130 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0050 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02976 | hp1 | a0037 | c0041 | t0001 | g0242 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02976 | hp2 | a0038 | c0055 | t0009 | g0092 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03017 | hp2 | a0019 | c0025 | t0002 | g0078 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03041 | hp1 | a0016 | c0040 | t0001 | g0244 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03041 | hp2 | a0003 | c0008 | t0003 | g0306 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03130 | hp1 | a0007 | c0009 | t0001 | g0261 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03130 | hp2 | a0001 | c0054 | t0001 | g0263 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03139 | hp1 | a0039 | c0029 | t0001 | g0301 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03139 | hp2 | a0040 | c0033 | t0003 | g0311 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03195 | hp1 | a0001 | c0003 | t0002 | g0069 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03195 | hp2 | a0021 | c0026 | t0003 | g0330 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03209 | hp1 | a0007 | c0009 | t0001 | g0262 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0291 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03225 | hp1 | a0001 | c0003 | t0002 | g0068 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03239 | hp1 | a0010 | c0013 | t0004 | g0335 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03239 | hp2 | a0001 | c0003 | t0005 | g0123 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03453 | hp1 | a0016 | c0038 | t0001 | g0243 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03453 | hp2 | a0001 | c0051 | t0002 | g0055 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03486 | hp1 | a0004 | c0045 | t0001 | g0280 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03486 | hp2 | a0011 | c0015 | t0006 | g0319 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03491 | hp2 | a0010 | c0013 | t0004 | g0336 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0119 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03492 | hp2 | a0010 | c0013 | t0004 | g0334 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03516 | hp1 | a0003 | c0023 | t0003 | g0326 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03516 | hp2 | a0007 | c0009 | t0001 | g0283 | AFR | ESN | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03540 | hp1 | a0001 | c0003 | t0002 | g0006 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03540 | hp2 | a0001 | c0003 | t0002 | g0086 | AFR | GWD | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03579 | hp1 | a0001 | c0003 | t0002 | g0067 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03579 | hp2 | a0001 | c0003 | t0002 | g0060 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0033 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03669 | hp1 | a0002 | c0061 | t0001 | g0177 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03669 | hp2 | a0001 | c0012 | t0001 | g0145 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03688 | hp1 | a0001 | c0004 | t0001 | g0268 | SAS | STU | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03704 | hp2 | a0001 | c0012 | t0001 | g0144 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03710 | hp1 | a0009 | c0011 | t0001 | g0235 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03834 | hp1 | a0008 | c0010 | t0001 | g0272 | SAS | BEB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03834 | hp2 | a0010 | c0013 | t0004 | g0333 | SAS | BEB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG04115 | hp1 | a0010 | c0013 | t0004 | g0337 | SAS | STU | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG04115 | hp2 | a0001 | c0003 | t0002 | g0084 | SAS | STU | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG04184 | hp1 | a0001 | c0003 | t0002 | g0089 | SAS | BEB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG04184 | hp2 | a0001 | c0062 | t0001 | g0225 | SAS | BEB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG04199 | hp1 | a0042 | c0065 | t0001 | g0231 | SAS | STU | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0035 | SAS | STU | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18522 | hp1 | a0001 | c0003 | t0002 | g0057 | AFR | YRI | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18522 | hp2 | a0001 | c0003 | t0002 | g0006 | AFR | YRI | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18612 | hp1 | a0004 | c0005 | t0001 | g0023 | EAS | CHB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18906 | hp1 | a0008 | c0052 | t0002 | g0054 | AFR | YRI | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18906 | hp2 | a0003 | c0020 | t0003 | g0026 | AFR | YRI | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18940 | hp1 | a0005 | c0006 | t0001 | g0255 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18942 | hp1 | a0001 | c0018 | t0001 | g0159 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18942 | hp2 | a0043 | c0039 | t0001 | g0249 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18943 | hp2 | a0012 | c0016 | t0001 | g0253 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18944 | hp2 | a0001 | c0004 | t0001 | g0025 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18947 | hp1 | a0013 | c0017 | t0001 | g0187 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18947 | hp2 | a0008 | c0010 | t0002 | g0106 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18948 | hp1 | a0008 | c0010 | t0001 | g0267 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18949 | hp2 | a0012 | c0016 | t0001 | g0300 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18950 | hp2 | a0001 | c0004 | t0002 | g0115 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18952 | hp1 | a0017 | c0024 | t0001 | g0252 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18954 | hp2 | a0018 | c0028 | t0001 | g0133 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18956 | hp2 | a0001 | c0004 | t0002 | g0094 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18959 | hp2 | a0001 | c0004 | t0002 | g0042 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18960 | hp1 | a0001 | c0027 | t0001 | g0238 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18960 | hp2 | a0005 | c0006 | t0001 | g0005 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18964 | hp2 | a0004 | c0005 | t0001 | g0281 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18966 | hp1 | a0001 | c0018 | t0001 | g0180 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18966 | hp2 | a0017 | c0037 | t0001 | g0257 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18967 | hp1 | a0005 | c0006 | t0001 | g0005 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18967 | hp2 | a0004 | c0005 | t0001 | g0295 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18973 | hp2 | a0004 | c0005 | t0001 | g0294 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18977 | hp1 | a0005 | c0006 | t0001 | g0022 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18977 | hp2 | a0044 | c0046 | t0002 | g0040 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18979 | hp1 | a0004 | c0005 | t0001 | g0276 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18982 | hp1 | a0001 | c0004 | t0001 | g0270 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18989 | hp2 | a0004 | c0005 | t0001 | g0023 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18991 | hp1 | a0005 | c0006 | t0001 | g0258 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18993 | hp2 | a0005 | c0006 | t0001 | g0005 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18994 | hp1 | a0001 | c0004 | t0001 | g0269 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18998 | hp1 | a0008 | c0010 | t0002 | g0098 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18999 | hp1 | a0005 | c0006 | t0001 | g0022 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18999 | hp2 | a0008 | c0010 | t0001 | g0286 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19000 | hp1 | a0008 | c0010 | t0001 | g0287 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19000 | hp2 | a0001 | c0004 | t0001 | g0292 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19002 | hp2 | a0001 | c0027 | t0001 | g0181 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19004 | hp1 | a0001 | c0004 | t0001 | g0284 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19005 | hp1 | a0045 | c0036 | t0001 | g0250 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19011 | hp2 | a0001 | c0004 | t0002 | g0107 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19012 | hp1 | a0013 | c0017 | t0001 | g0227 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19030 | hp1 | a0001 | c0003 | t0002 | g0082 | AFR | LWK | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19030 | hp2 | a0001 | c0003 | t0002 | g0070 | AFR | LWK | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19043 | hp1 | a0007 | c0009 | t0001 | g0260 | AFR | LWK | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19043 | hp2 | a0003 | c0031 | t0007 | g0027 | AFR | LWK | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19055 | hp2 | a0006 | c0007 | t0001 | g0157 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19056 | hp2 | a0005 | c0006 | t0001 | g0005 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19060 | hp2 | a0001 | c0004 | t0001 | g0285 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19064 | hp1 | a0001 | c0004 | t0001 | g0288 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19065 | hp1 | a0001 | c0018 | t0001 | g0214 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19067 | hp1 | a0001 | c0004 | t0001 | g0299 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19077 | hp1 | a0006 | c0007 | t0001 | g0178 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19079 | hp2 | a0001 | c0004 | t0001 | g0025 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19081 | hp1 | a0017 | c0024 | t0001 | g0247 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19081 | hp2 | a0013 | c0017 | t0001 | g0175 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19082 | hp2 | a0001 | c0018 | t0001 | g0191 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19084 | hp1 | a0005 | c0006 | t0001 | g0256 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19084 | hp2 | a0001 | c0004 | t0002 | g0039 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19088 | hp1 | a0004 | c0005 | t0001 | g0275 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19089 | hp1 | a0046 | c0060 | t0001 | g0173 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19089 | hp2 | a0005 | c0006 | t0001 | g0248 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19091 | hp2 | a0008 | c0064 | t0001 | g0206 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19240 | hp1 | a0001 | c0004 | t0002 | g0053 | AFR | YRI | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA19240 | hp2 | a0003 | c0020 | t0003 | g0026 | AFR | YRI | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA20129 | hp1 | a0001 | c0004 | t0001 | g0271 | AFR | ASW | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA20129 | hp2 | a0047 | c0069 | t0002 | g0093 | AFR | ASW | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA20752 | hp1 | a0009 | c0011 | t0001 | g0172 | EUR | TSI | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA20752 | hp2 | a0001 | c0003 | t0010 | g0091 | EUR | TSI | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA20805 | hp1 | a0014 | c0021 | t0002 | g0080 | EUR | TSI | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA20805 | hp2 | a0001 | c0004 | t0002 | g0011 | EUR | TSI | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA20905 | hp1 | a0001 | c0004 | t0001 | g0302 | SAS | GIH | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | GIH | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01123 | hp1 | a0001 | c0003 | t0002 | g0013 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02109 | hp1 | a0003 | c0008 | t0003 | g0309 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02109 | hp2 | a0021 | c0026 | t0003 | g0329 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02486 | hp1 | a0001 | c0003 | t0002 | g0013 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02486 | hp2 | a0008 | c0050 | t0002 | g0058 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0264 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG02559 | hp2 | a0028 | c0073 | t0001 | g0132 | AFR | ACB | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03471 | hp1 | a0041 | c0030 | t0003 | g0313 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG03471 | hp2 | a0003 | c0020 | t0003 | g0318 | AFR | MSL | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | USA | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
HG06807 | hp2 | a0004 | c0005 | t0001 | g0278 | AFR | USA | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18955 | hp1 | a0012 | c0016 | t0001 | g0254 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | USA | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA20300 | hp2 | a0003 | c0014 | t0003 | g0322 | AFR | USA | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA21309 | hp1 | a0003 | c0008 | t0003 | g0316 | AFR | LWK | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
NA21309 | hp2 | a0048 | c0034 | t0003 | g0305 | AFR | LWK | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0161 | REF | REF | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
homoSapiens | grch38p0 | a0007 | c0009 | t0001 | g0266 | REF | REF | CEP131_chr17_81184596_81227965 | CEP131 | chr17 | 81184596 | 81227965 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:81189958 | G | A | 6 | a0005 a0008 a0012 others(3): Show |
27 | HG01358.hp2 HG02080.hp1 HG02129.hp2 others(24): Show |
missense_variant | MODERATE | c.3125C>T | p.Ala1042Val | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 25/26 | 3339/3630 | 3125/3243 | 1042/1080 | chr17 | 81189958 | |||
chr17:81190688 | C | T | 2 | a0014 a0034 |
4 | HG01070.hp1 HG01255.hp1 HG02818.hp2 others(1): Show |
missense_variant | MODERATE | c.3058G>A | p.Ala1020Thr | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/26 | 3272/3630 | 3058/3243 | 1020/1080 | chr17 | 81190688 | |||
chr17:81190917 | T | C | 1 | a0022 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.2933A>G | p.Asp978Gly | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 23/26 | 3147/3630 | 2933/3243 | 978/1080 | chr17 | 81190917 | |||
chr17:81190929 | C | G | 1 | a0046 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.2921G>C | p.Arg974Pro | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 23/26 | 3135/3630 | 2921/3243 | 974/1080 | chr17 | 81190929 | |||
chr17:81190930 | G | C | 1 | a0046 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.2920C>G | p.Arg974Gly | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 23/26 | 3134/3630 | 2920/3243 | 974/1080 | chr17 | 81190930 | |||
chr17:81191005 | A | C | 1 | a0046 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.2845T>G | p.Ser949Ala | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 23/26 | 3059/3630 | 2845/3243 | 949/1080 | chr17 | 81191005 | |||
chr17:81191006 | G | C | 1 | a0044 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.2844C>G | p.Cys948Trp | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 23/26 | 3058/3630 | 2844/3243 | 948/1080 | chr17 | 81191006 | |||
chr17:81191079 | T | C | 3 | a0011 a0038 a0048 |
6 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(3): Show |
missense_variant | MODERATE | c.2771A>G | p.Lys924Arg | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 23/26 | 2985/3630 | 2771/3243 | 924/1080 | chr17 | 81191079 | |||
chr17:81191216 | C | G | 2 | a0024 a0040 |
2 | HG01255.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.2742G>C | p.Glu914Asp | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 22/26 | 2956/3630 | 2742/3243 | 914/1080 | chr17 | 81191216 | |||
chr17:81193944 | C | T | 1 | a0013 | 4 | HG02132.hp2 NA18947.hp1 NA19012.hp1 others(1): Show |
missense_variant | MODERATE | c.2303G>A | p.Arg768His | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/26 | 2517/3630 | 2303/3243 | 768/1080 | chr17 | 81193944 | |||
chr17:81193989 | C | T | 1 | a0041 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.2258G>A | p.Arg753Gln | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/26 | 2472/3630 | 2258/3243 | 753/1080 | chr17 | 81193989 | |||
chr17:81195848 | G | A | 1 | a0042 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.2003C>T | p.Ala668Val | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/26 | 2217/3630 | 2003/3243 | 668/1080 | chr17 | 81195848 | |||
chr17:81195870 | C | T | 2 | a0009 a0022 |
6 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(3): Show |
missense_variant | MODERATE | c.1981G>A | p.Glu661Lys | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/26 | 2195/3630 | 1981/3243 | 661/1080 | chr17 | 81195870 | |||
chr17:81196708 | A | G | 1 | a0023 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.1892T>C | p.Ile631Thr | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/26 | 2106/3630 | 1892/3243 | 631/1080 | chr17 | 81196708 | |||
chr17:81196750 | C | T | 1 | a0033 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1850G>A | p.Arg617Lys | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/26 | 2064/3630 | 1850/3243 | 617/1080 | chr17 | 81196750 | |||
chr17:81196778 | C | T | 7 | a0002 a0015 a0032 others(4): Show |
59 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(56): Show |
missense_variant | MODERATE | c.1822G>A | p.Ala608Thr | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/26 | 2036/3630 | 1822/3243 | 608/1080 | chr17 | 81196778 | |||
chr17:81198159 | G | A | 2 | a0010 a0033 |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
missense_variant | MODERATE | c.1426C>T | p.Arg476Cys | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 12/26 | 1640/3630 | 1426/3243 | 476/1080 | chr17 | 81198159 | |||
chr17:81198167 | A | G | 44 | a0001 a0002 a0003 others(41): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
missense_variant | MODERATE | c.1418T>C | p.Val473Ala | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 12/26 | 1632/3630 | 1418/3243 | 473/1080 | chr17 | 81198167 | |||
chr17:81198171 | C | T | 1 | a0044 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.1414G>A | p.Asp472Asn | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 12/26 | 1628/3630 | 1414/3243 | 472/1080 | chr17 | 81198171 | |||
chr17:81198906 | G | A | 2 | a0016 a0037 |
4 | HG02895.hp2 HG02976.hp1 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.1258C>T | p.Pro420Ser | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/26 | 1472/3630 | 1258/3243 | 420/1080 | chr17 | 81198906 | |||
chr17:81198911 | G | A | 1 | a0019 | 2 | HG01106.hp1 HG03017.hp2 |
missense_variant | MODERATE | c.1253C>T | p.Pro418Leu | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/26 | 1467/3630 | 1253/3243 | 418/1080 | chr17 | 81198911 | |||
chr17:81198956 | G | A | 1 | a0048 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1208C>T | p.Ala403Val | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/26 | 1422/3630 | 1208/3243 | 403/1080 | chr17 | 81198956 | |||
chr17:81199384 | T | C | 45 | a0001 a0002 a0003 others(42): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
missense_variant | MODERATE | c.1189A>G | p.Thr397Ala | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 10/26 | 1403/3630 | 1189/3243 | 397/1080 | chr17 | 81199384 | |||
chr17:81200381 | C | T | 1 | a0006 | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp2 others(6): Show |
missense_variant | MODERATE | c.854G>A | p.Arg285Gln | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/26 | 1068/3630 | 854/3243 | 285/1080 | chr17 | 81200381 | |||
chr17:81200382 | G | A | 4 | a0012 a0020 a0043 others(1): Show |
8 | HG01358.hp2 HG02080.hp1 HG02129.hp2 others(5): Show |
missense_variant | MODERATE | c.853C>T | p.Arg285Trp | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/26 | 1067/3630 | 853/3243 | 285/1080 | chr17 | 81200382 | |||
chr17:81200421 | T | C | 46 | a0001 a0002 a0003 others(43): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
missense_variant | MODERATE | c.814A>G | p.Thr272Ala | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/26 | 1028/3630 | 814/3243 | 272/1080 | chr17 | 81200421 | |||
chr17:81202271 | G | A | 2 | a0021 a0025 |
3 | HG01891.hp1 HG02109.hp2 HG03195.hp2 |
missense_variant | MODERATE | c.757C>T | p.Arg253Trp | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/26 | 971/3630 | 757/3243 | 253/1080 | chr17 | 81202271 | |||
chr17:81202342 | A | G | 7 | a0010 a0024 a0026 others(4): Show |
11 | HG01255.hp2 HG01891.hp2 HG02572.hp1 others(8): Show |
missense_variant | MODERATE | c.686T>C | p.Leu229Pro | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/26 | 900/3630 | 686/3243 | 229/1080 | chr17 | 81202342 | |||
chr17:81206832 | G | A | 1 | a0036 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.427C>T | p.Arg143Trp | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/26 | 641/3630 | 427/3243 | 143/1080 | chr17 | 81206832 | |||
chr17:81207130 | C | T | 1 | a0045 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.382G>A | p.Val128Ile | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 4/26 | 596/3630 | 382/3243 | 128/1080 | chr17 | 81207130 | |||
chr17:81207234 | G | A | 1 | a0018 | 2 | HG00423.hp1 NA18954.hp2 |
missense_variant | MODERATE | c.278C>T | p.Thr93Met | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 4/26 | 492/3630 | 278/3243 | 93/1080 | chr17 | 81207234 | |||
chr17:81208997 | T | C | 10 | a0010 a0015 a0024 others(7): Show |
16 | HG01255.hp2 HG01891.hp2 HG02258.hp2 others(13): Show |
missense_variant | MODERATE | c.203A>G | p.Gln68Arg | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/26 | 417/3630 | 203/3243 | 68/1080 | chr17 | 81208997 | |||
chr17:81219902 | C | T | 8 | a0005 a0012 a0016 others(5): Show |
24 | HG01358.hp2 HG02630.hp1 HG02895.hp2 others(21): Show |
missense_variant | MODERATE | c.155G>A | p.Ser52Asn | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/26 | 369/3630 | 155/3243 | 52/1080 | chr17 | 81219902 | |||
chr17:81219927 | G | A | 1 | a0047 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.130C>T | p.Arg44Cys | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/26 | 344/3630 | 130/3243 | 44/1080 | chr17 | 81219927 | |||
chr17:81219930 | C | T | 7 | a0003 a0011 a0024 others(4): Show |
27 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(24): Show |
missense_variant | MODERATE | c.127G>A | p.Val43Ile | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/26 | 341/3630 | 127/3243 | 43/1080 | chr17 | 81219930 | |||
chr17:81219936 | G | A | 5 | a0015 a0025 a0026 others(2): Show |
7 | HG01891.hp1 HG01891.hp2 HG02258.hp2 others(4): Show |
missense_variant | MODERATE | c.121C>T | p.Pro41Ser | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/26 | 335/3630 | 121/3243 | 41/1080 | chr17 | 81219936 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:81190907 | C | T | 8 | a0005c0006 a0008c0010 a0008c0064 others(5): Show |
26 | HG01358.hp2 HG02080.hp1 HG02129.hp2 others(23): Show |
splice_region_variant&synonymous_variant | LOW | c.2943G>A | p.Ala981Ala | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 23/26 | 3157/3630 | 2943/3243 | 981/1080 | chr17 | 81190907 | |||
chr17:81190931 | C | T | 1 | a0046c0060 | 1 | NA19089.hp1 | synonymous_variant | LOW | c.2919G>A | p.Glu973Glu | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 23/26 | 3133/3630 | 2919/3243 | 973/1080 | chr17 | 81190931 | |||
chr17:81191030 | C | T | 1 | a0003c0031 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.2820G>A | p.Ser940Ser | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 23/26 | 3034/3630 | 2820/3243 | 940/1080 | chr17 | 81191030 | |||
chr17:81191036 | C | T | 2 | a0010c0013 a0033c0068 |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
synonymous_variant | LOW | c.2814G>A | p.Glu938Glu | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 23/26 | 3028/3630 | 2814/3243 | 938/1080 | chr17 | 81191036 | |||
chr17:81191201 | G | A | 1 | a0031c0070 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.2757C>T | p.Ala919Ala | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 22/26 | 2971/3630 | 2757/3243 | 919/1080 | chr17 | 81191201 | |||
chr17:81192324 | C | T | 4 | a0016c0038 a0016c0040 a0016c0042 others(1): Show |
4 | HG01891.hp2 HG02895.hp2 HG03041.hp1 others(1): Show |
synonymous_variant | LOW | c.2616G>A | p.Arg872Arg | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/26 | 2830/3630 | 2616/3243 | 872/1080 | chr17 | 81192324 | |||
chr17:81192336 | G | A | 1 | a0001c0012 | 5 | HG00280.hp2 HG01515.hp2 HG01517.hp2 others(2): Show |
synonymous_variant | LOW | c.2604C>T | p.Ala868Ala | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/26 | 2818/3630 | 2604/3243 | 868/1080 | chr17 | 81192336 | |||
chr17:81192357 | C | T | 1 | a0001c0018 | 4 | NA18942.hp1 NA18966.hp1 NA19065.hp1 others(1): Show |
synonymous_variant | LOW | c.2583G>A | p.Leu861Leu | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/26 | 2797/3630 | 2583/3243 | 861/1080 | chr17 | 81192357 | |||
chr17:81192584 | C | T | 20 | a0001c0051 a0001c0058 a0002c0002 others(17): Show |
77 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(74): Show |
synonymous_variant | LOW | c.2439G>A | p.Ala813Ala | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 20/26 | 2653/3630 | 2439/3243 | 813/1080 | chr17 | 81192584 | |||
chr17:81195841 | G | A | 13 | a0002c0002 a0002c0047 a0002c0061 others(10): Show |
67 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(64): Show |
synonymous_variant | LOW | c.2010C>T | p.His670His | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/26 | 2224/3630 | 2010/3243 | 670/1080 | chr17 | 81195841 | |||
chr17:81195934 | C | T | 1 | a0002c0047 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1917G>A | p.Lys639Lys | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/26 | 2131/3630 | 1917/3243 | 639/1080 | chr17 | 81195934 | |||
chr17:81196776 | C | T | 11 | a0001c0003 a0001c0062 a0003c0020 others(8): Show |
65 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(62): Show |
synonymous_variant | LOW | c.1824G>A | p.Ala608Ala | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/26 | 2038/3630 | 1824/3243 | 608/1080 | chr17 | 81196776 | |||
chr17:81196824 | C | T | 1 | a0016c0040 | 1 | HG03041.hp1 | splice_region_variant&synonymous_variant | LOW | c.1776G>A | p.Ala592Ala | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/26 | 1990/3630 | 1776/3243 | 592/1080 | chr17 | 81196824 | |||
chr17:81197032 | C | T | 3 | a0001c0027 a0010c0013 a0033c0068 |
8 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(5): Show |
synonymous_variant | LOW | c.1671G>A | p.Pro557Pro | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 14/26 | 1885/3630 | 1671/3243 | 557/1080 | chr17 | 81197032 | |||
chr17:81198916 | T | G | 3 | a0001c0054 a0003c0008 a0003c0020 |
12 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
synonymous_variant | LOW | c.1248A>C | p.Ser416Ser | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/26 | 1462/3630 | 1248/3243 | 416/1080 | chr17 | 81198916 | |||
chr17:81198922 | G | A | 1 | a0001c0019 | 4 | HG00741.hp2 HG01934.hp1 HG01975.hp2 others(1): Show |
synonymous_variant | LOW | c.1242C>T | p.Ser414Ser | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/26 | 1456/3630 | 1242/3243 | 414/1080 | chr17 | 81198922 | |||
chr17:81198946 | G | A | 3 | a0011c0015 a0038c0055 a0039c0029 |
6 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(3): Show |
synonymous_variant | LOW | c.1218C>T | p.Pro406Pro | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/26 | 1432/3630 | 1218/3243 | 406/1080 | chr17 | 81198946 | |||
chr17:81199424 | T | C | 61 | a0001c0001 a0001c0003 a0001c0004 others(58): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
synonymous_variant | LOW | c.1149A>G | p.Thr383Thr | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 10/26 | 1363/3630 | 1149/3243 | 383/1080 | chr17 | 81199424 | |||
chr17:81207224 | T | C | 13 | a0001c0058 a0010c0013 a0015c0022 others(10): Show |
19 | HG01255.hp2 HG01891.hp2 HG02145.hp2 others(16): Show |
synonymous_variant | LOW | c.288A>G | p.Thr96Thr | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 4/26 | 502/3630 | 288/3243 | 96/1080 | chr17 | 81207224 | |||
chr17:81208978 | T | C | 18 | a0001c0001 a0001c0012 a0001c0018 others(15): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
synonymous_variant | LOW | c.222A>G | p.Arg74Arg | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/26 | 436/3630 | 222/3243 | 74/1080 | chr17 | 81208978 | |||
chr17:81219949 | G | A | 1 | a0001c0074 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.108C>T | p.Ala36Ala | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/26 | 322/3630 | 108/3243 | 36/1080 | chr17 | 81219949 | |||
chr17:81220024 | C | T | 1 | a0039c0029 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.33G>A | p.Pro11Pro | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/26 | 247/3630 | 33/3243 | 11/1080 | chr17 | 81220024 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:81189681 | C | T | 2 | a0004c0044t0011 a0019c0025t0008 |
2 | HG01106.hp1 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*88G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 26/26 | 88 | chr17 | 81189681 | ||||||
chr17:81189714 | G | A | 2 | a0011c0015t0006 a0038c0055t0009 |
5 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*55C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 26/26 | 55 | chr17 | 81189714 | ||||||
chr17:81220067 | G | A | 1 | a0001c0003t0010 | 1 | NA20752.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/26 | 11 | chr17 | 81220067 | ||||||
chr17:81222784 | G | A | 1 | a0002c0002t0012 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/26 | 2728 | chr17 | 81222784 | ||||||
chr17:81222785 | C | A | 12 | a0001c0058t0003 a0003c0008t0003 a0003c0014t0003 others(9): Show |
29 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-34G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/26 | 2729 | chr17 | 81222785 | ||||||
chr17:81222804 | T | A | 1 | a0001c0003t0005 | 5 | HG00099.hp1 HG00733.hp2 HG01516.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-53A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/26 | chr17 | 81222804 | |||||||
chr17:81222844 | T | A | 2 | a0010c0013t0004 a0033c0068t0004 |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-93A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/26 | 2788 | chr17 | 81222844 | ||||||
chr17:81222862 | C | G | 19 | a0001c0003t0002 a0001c0003t0005 a0001c0003t0010 others(16): Show |
122 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
5_prime_UTR_variant | MODIFIER | c.-111G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/26 | 2806 | chr17 | 81222862 | ||||||
chr17:81222924 | A | G | 1 | a0003c0031t0007 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-173T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/26 | 2868 | chr17 | 81222924 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:81189849 | G | A | 68 | a0001c0001t0001g0019 a0001c0001t0001g0185 a0001c0001t0001g0186 others(65): Show |
77 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(74): Show |
splice_region_variant&intron_variant | LOW | c.3169-6C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 25/25 | chr17 | 81189849 | |||||||
chr17:81190029 | G | C | 15 | a0003c0031t0007g0027 a0010c0013t0004g0333 a0010c0013t0004g0334 others(12): Show |
15 | HG01255.hp2 HG01891.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.3108-54C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190029 | |||||||
chr17:81190062 | C | T | 2 | a0001c0003t0005g0121 a0001c0003t0005g0124 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3108-87G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190062 | |||||||
chr17:81190088 | G | T | 1 | a0008c0010t0002g0106 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3108-113C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190088 | |||||||
chr17:81190089 | C | T | 1 | a0008c0010t0002g0106 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3108-114G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190089 | |||||||
chr17:81190174 | T | G | 1 | a0003c0008t0003g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3108-199A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190174 | |||||||
chr17:81190175 | A | G | 1 | a0003c0008t0003g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3108-200T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190175 | |||||||
chr17:81190237 | C | G | 1 | a0004c0045t0001g0280 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3108-262G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190237 | |||||||
chr17:81190250 | T | C | 71 | a0001c0003t0010g0091 a0001c0004t0002g0053 a0001c0051t0002g0055 others(68): Show |
81 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.3108-275A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190250 | |||||||
chr17:81190288 | G | A | 2 | a0024c0035t0003g0312 a0040c0033t0003g0311 |
2 | HG01255.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3108-313C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190288 | |||||||
chr17:81190309 | C | A | 1 | a0003c0008t0003g0317 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3107+330G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190309 | |||||||
chr17:81190334 | C | T | 1 | a0003c0008t0003g0316 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3107+305G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190334 | |||||||
chr17:81190335 | G | A | 1 | a0029c0067t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3107+304C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190335 | |||||||
chr17:81190408 | G | A | 1 | a0036c0057t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3107+231C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190408 | |||||||
chr17:81190510 | T | C | 68 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(65): Show |
78 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.3107+129A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190510 | |||||||
chr17:81190590 | G | A | 54 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(51): Show |
64 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.3107+49C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190590 | |||||||
chr17:81190608 | C | T | 1 | a0012c0016t0001g0251 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3107+31G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 24/25 | chr17 | 81190608 | |||||||
chr17:81191093 | G | T | 1 | a0002c0061t0001g0177 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2766-9C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 22/25 | chr17 | 81191093 | |||||||
chr17:81191139 | C | T | 3 | a0001c0003t0002g0070 a0001c0003t0002g0071 a0001c0003t0002g0073 |
3 | HG02895.hp1 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2765+54G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 22/25 | chr17 | 81191139 | |||||||
chr17:81191150 | G | C | 58 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(55): Show |
68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2765+43C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 22/25 | chr17 | 81191150 | |||||||
chr17:81191339 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG01928.hp1 | splice_region_variant&intron_variant | LOW | c.2623-4C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191339 | |||||||
chr17:81191371 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(128): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2623-36C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191371 | |||||||
chr17:81191382 | G | A | 2 | a0024c0035t0003g0312 a0040c0033t0003g0311 |
2 | HG01255.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2623-47C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191382 | |||||||
chr17:81191384 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2623-49C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191384 | |||||||
chr17:81191425 | C | T | 58 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(55): Show |
68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2623-90G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191425 | |||||||
chr17:81191521 | C | T | 2 | a0024c0035t0003g0312 a0040c0033t0003g0311 |
2 | HG01255.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2623-186G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191521 | |||||||
chr17:81191525 | C | T | 1 | a0016c0038t0001g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2623-190G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191525 | |||||||
chr17:81191598 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2623-263G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191598 | |||||||
chr17:81191660 | C | A | 2 | a0004c0045t0001g0280 a0029c0067t0001g0126 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2623-325G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191660 | |||||||
chr17:81191723 | G | A | 1 | a0001c0004t0002g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2623-388C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191723 | |||||||
chr17:81191730 | A | T | 3 | a0002c0002t0002g0014 a0002c0002t0002g0015 a0002c0002t0002g0120 |
5 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2623-395T>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191730 | |||||||
chr17:81191756 | G | C | 58 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(55): Show |
68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2623-421C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191756 | |||||||
chr17:81191818 | C | G | 58 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(55): Show |
68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2623-483G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191818 | |||||||
chr17:81191886 | G | A | 58 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(55): Show |
68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2622+432C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191886 | |||||||
chr17:81191897 | G | A | 1 | a0036c0057t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2622+421C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191897 | |||||||
chr17:81191969 | G | T | 2 | a0003c0008t0003g0306 a0003c0008t0003g0328 |
2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2622+349C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81191969 | |||||||
chr17:81192040 | G | A | 1 | a0003c0023t0003g0327 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2622+278C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81192040 | |||||||
chr17:81192056 | C | T | 49 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(46): Show |
59 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2622+262G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81192056 | |||||||
chr17:81192057 | G | A | 15 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0004t0001g0025 others(12): Show |
16 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.2622+261C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81192057 | |||||||
chr17:81192131 | A | G | 1 | a0020c0056t0001g0148 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2622+187T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81192131 | |||||||
chr17:81192172 | A | G | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(320): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.2622+146T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81192172 | |||||||
chr17:81192178 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2622+140G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81192178 | |||||||
chr17:81192224 | A | G | 3 | a0002c0002t0002g0095 a0002c0002t0002g0109 a0002c0002t0002g0110 |
3 | NA18964.hp1 NA18994.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2622+94T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81192224 | |||||||
chr17:81192303 | T | C | 138 | a0001c0003t0001g0264 a0001c0003t0001g0293 a0001c0003t0002g0006 others(135): Show |
155 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.2622+15A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 21/25 | chr17 | 81192303 | |||||||
chr17:81192401 | C | T | 58 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(55): Show |
68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2548-9G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 20/25 | chr17 | 81192401 | |||||||
chr17:81192428 | C | A | 1 | a0019c0025t0002g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2548-36G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 20/25 | chr17 | 81192428 | |||||||
chr17:81192629 | T | A | 1 | a0001c0003t0002g0081 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2430-36A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 19/25 | chr17 | 81192629 | |||||||
chr17:81192660 | G | A | 2 | a0016c0038t0001g0243 a0026c0072t0001g0303 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2430-67C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 19/25 | chr17 | 81192660 | |||||||
chr17:81192662 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2430-69C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 19/25 | chr17 | 81192662 | |||||||
chr17:81192667 | AG | A | 58 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(55): Show |
68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2429+68delC | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 19/25 | chr17 | 81192667 | |||||||
chr17:81192673 | C | T | 67 | a0001c0051t0002g0055 a0001c0058t0003g0331 a0002c0002t0001g0024 others(64): Show |
77 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.2429+63G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 19/25 | chr17 | 81192673 | |||||||
chr17:81192694 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2429+42G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 19/25 | chr17 | 81192694 | |||||||
chr17:81192848 | G | A | 8 | a0001c0051t0002g0055 a0003c0014t0003g0314 a0003c0014t0003g0322 others(5): Show |
8 | HG02280.hp2 HG02615.hp1 HG02615.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.2322-5C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81192848 | |||||||
chr17:81192905 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2322-62G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81192905 | |||||||
chr17:81192920 | C | T | 1 | a0001c0004t0001g0290 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2322-77G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81192920 | |||||||
chr17:81193010 | G | A | 58 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(55): Show |
68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2322-167C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193010 | |||||||
chr17:81193028 | G | A | 39 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0004t0001g0025 others(36): Show |
44 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.2322-185C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193028 | |||||||
chr17:81193110 | C | T | 1 | a0001c0003t0002g0089 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2322-267G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193110 | |||||||
chr17:81193245 | G | A | 1 | a0004c0005t0001g0275 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2322-402C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193245 | |||||||
chr17:81193282 | G | A | 2 | a0001c0003t0002g0085 a0001c0003t0002g0089 |
2 | HG00735.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2322-439C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193282 | |||||||
chr17:81193315 | T | C | 192 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0003t0001g0264 others(189): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.2322-472A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193315 | |||||||
chr17:81193316 | G | C | 69 | a0001c0003t0001g0264 a0001c0003t0001g0293 a0001c0003t0002g0006 others(66): Show |
76 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.2322-473C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193316 | |||||||
chr17:81193406 | C | T | 1 | a0048c0034t0003g0305 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2321+520G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193406 | |||||||
chr17:81193419 | G | C | 1 | a0001c0003t0002g0081 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2321+507C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193419 | |||||||
chr17:81193448 | G | A | 58 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(55): Show |
68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2321+478C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193448 | |||||||
chr17:81193494 | G | C | 39 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0004t0001g0025 others(36): Show |
44 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.2321+432C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193494 | |||||||
chr17:81193546 | G | C | 1 | a0002c0002t0002g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2321+380C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193546 | |||||||
chr17:81193548 | G | A | 1 | a0003c0031t0007g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2321+378C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193548 | |||||||
chr17:81193610 | T | C | 58 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(55): Show |
68 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2321+316A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193610 | |||||||
chr17:81193660 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2321+266T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193660 | |||||||
chr17:81193684 | G | A | 4 | a0001c0004t0002g0075 a0021c0026t0003g0329 a0021c0026t0003g0330 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2321+242C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193684 | |||||||
chr17:81193715 | G | A | 2 | a0003c0031t0007g0027 a0008c0010t0001g0272 |
2 | HG03834.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2321+211C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193715 | |||||||
chr17:81193739 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2321+187G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193739 | |||||||
chr17:81193754 | G | A | 1 | a0001c0018t0001g0214 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2321+172C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193754 | |||||||
chr17:81193831 | G | A | 1 | a0008c0010t0001g0287 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2321+95C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193831 | |||||||
chr17:81193852 | C | A | 9 | a0001c0051t0002g0055 a0001c0058t0003g0331 a0003c0014t0003g0314 others(6): Show |
9 | HG02145.hp2 HG02280.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2321+74G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 18/25 | chr17 | 81193852 | |||||||
chr17:81194195 | A | G | 8 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0005g0121 others(5): Show |
10 | HG00099.hp1 HG00733.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.2120-68T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194195 | |||||||
chr17:81194254 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2120-127T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194254 | |||||||
chr17:81194300 | A | G | 3 | a0002c0002t0002g0014 a0002c0002t0002g0015 a0002c0002t0002g0120 |
5 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2120-173T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194300 | |||||||
chr17:81194319 | G | A | 49 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0004t0001g0025 others(46): Show |
54 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.2120-192C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194319 | |||||||
chr17:81194351 | G | A | 48 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(45): Show |
58 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.2120-224C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194351 | |||||||
chr17:81194374 | C | T | 1 | a0002c0002t0002g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2120-247G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194374 | |||||||
chr17:81194407 | G | A | 17 | a0002c0002t0001g0024 a0002c0002t0002g0014 a0002c0002t0002g0015 others(14): Show |
20 | HG00639.hp1 HG02258.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.2120-280C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194407 | |||||||
chr17:81194468 | A | C | 138 | a0001c0003t0001g0264 a0001c0003t0001g0293 a0001c0003t0002g0006 others(135): Show |
155 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.2120-341T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194468 | |||||||
chr17:81194643 | A | G | 29 | a0001c0004t0002g0075 a0002c0002t0001g0024 a0002c0002t0002g0014 others(26): Show |
31 | HG00639.hp1 HG01891.hp1 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2119+227T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194643 | |||||||
chr17:81194663 | G | C | 19 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0001t0001g0183 others(16): Show |
20 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.2119+207C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194663 | |||||||
chr17:81194698 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2119+172G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194698 | |||||||
chr17:81194699 | G | A | 2 | a0001c0003t0002g0012 a0001c0003t0002g0083 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2119+171C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194699 | |||||||
chr17:81194718 | G | A | 1 | a0003c0008t0003g0307 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2119+152C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194718 | |||||||
chr17:81194779 | A | G | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.2119+91T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194779 | |||||||
chr17:81194816 | C | T | 2 | a0024c0035t0003g0312 a0040c0033t0003g0311 |
2 | HG01255.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2119+54G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194816 | |||||||
chr17:81194817 | T | G | 1 | a0010c0013t0004g0333 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2119+53A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 17/25 | chr17 | 81194817 | |||||||
chr17:81195112 | C | CACACATG others(10): Show |
57 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(54): Show |
67 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2017-141_2017-140i others(19): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195112 | |||||||
chr17:81195136 | C | T | 2 | a0004c0045t0001g0280 a0029c0067t0001g0126 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2017-164G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195136 | |||||||
chr17:81195188 | C | A | 1 | a0002c0002t0002g0100 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2017-216G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195188 | |||||||
chr17:81195279 | T | A | 49 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(46): Show |
59 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2017-307A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195279 | |||||||
chr17:81195302 | C | T | 57 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(54): Show |
67 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2017-330G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195302 | |||||||
chr17:81195420 | G | A | 2 | a0001c0003t0002g0028 a0001c0003t0002g0029 |
2 | HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2016+415C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195420 | |||||||
chr17:81195538 | A | G | 323 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(320): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.2016+297T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195538 | |||||||
chr17:81195580 | C | T | 7 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(4): Show |
11 | NA18940.hp1 NA18952.hp1 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.2016+255G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195580 | |||||||
chr17:81195686 | C | T | 2 | a0024c0035t0003g0312 a0040c0033t0003g0311 |
2 | HG01255.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2016+149G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195686 | |||||||
chr17:81195752 | G | A | 49 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(46): Show |
59 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2016+83C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195752 | |||||||
chr17:81195811 | G | A | 1 | a0010c0013t0004g0333 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2016+24C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195811 | |||||||
chr17:81195816 | G | A | 1 | a0003c0031t0007g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2016+19C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 16/25 | chr17 | 81195816 | |||||||
chr17:81196037 | G | C | 57 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(54): Show |
67 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1900-86C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/25 | chr17 | 81196037 | |||||||
chr17:81196144 | C | T | 57 | a0002c0002t0001g0024 a0002c0002t0001g0273 a0002c0002t0002g0001 others(54): Show |
67 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1900-193G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/25 | chr17 | 81196144 | |||||||
chr17:81196177 | A | C | 1 | a0026c0072t0001g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1900-226T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/25 | chr17 | 81196177 | |||||||
chr17:81196339 | G | A | 1 | a0044c0046t0002g0040 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1899+362C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/25 | chr17 | 81196339 | |||||||
chr17:81196373 | C | CCTGGAGG others(12): Show |
1 | a0001c0018t0001g0214 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1899+309_1899+327d others(21): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/25 | chr17 | 81196373 | |||||||
chr17:81196409 | T | A | 1 | a0001c0058t0003g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1899+292A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/25 | chr17 | 81196409 | |||||||
chr17:81196467 | C | T | 16 | a0002c0002t0001g0024 a0002c0002t0002g0014 a0002c0002t0002g0015 others(13): Show |
19 | HG00639.hp1 HG02258.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.1899+234G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/25 | chr17 | 81196467 | |||||||
chr17:81196468 | G | A | 1 | a0032c0043t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1899+233C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/25 | chr17 | 81196468 | |||||||
chr17:81196663 | C | T | 2 | a0001c0003t0002g0006 a0001c0003t0002g0061 |
4 | HG01243.hp1 HG02723.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1899+38G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 15/25 | chr17 | 81196663 | |||||||
chr17:81196863 | C | A | 1 | a0006c0007t0001g0178 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1774-37G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 14/25 | chr17 | 81196863 | |||||||
chr17:81196915 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1773+15A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 14/25 | chr17 | 81196915 | |||||||
chr17:81196924 | C | T | 2 | a0024c0035t0003g0312 a0040c0033t0003g0311 |
2 | HG01255.hp2 HG03139.hp2 |
splice_region_variant&intron_variant | LOW | c.1773+6G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 14/25 | chr17 | 81196924 | |||||||
chr17:81197069 | C | T | 1 | a0001c0004t0001g0285 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1648-14G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197069 | |||||||
chr17:81197073 | C | T | 14 | a0001c0001t0001g0140 a0001c0001t0001g0153 a0001c0004t0001g0025 others(11): Show |
15 | HG00099.hp2 HG00423.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1648-18G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197073 | |||||||
chr17:81197082 | G | A | 1 | a0004c0044t0011g0297 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1648-27C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197082 | |||||||
chr17:81197102 | G | A | 1 | a0002c0002t0002g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1648-47C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197102 | |||||||
chr17:81197192 | G | T | 12 | a0002c0002t0001g0024 a0002c0002t0002g0050 a0002c0002t0002g0052 others(9): Show |
13 | HG00639.hp1 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1648-137C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197192 | |||||||
chr17:81197204 | C | T | 2 | a0016c0038t0001g0243 a0026c0072t0001g0303 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1648-149G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197204 | |||||||
chr17:81197236 | A | G | 7 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0057 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1648-181T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197236 | |||||||
chr17:81197250 | C | T | 2 | a0016c0040t0001g0244 a0016c0042t0001g0245 |
2 | HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1648-195G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197250 | |||||||
chr17:81197251 | C | T | 17 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(14): Show |
21 | HG02080.hp1 HG02129.hp2 NA18940.hp1 others(18): Show |
intron_variant | MODIFIER | c.1648-196G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197251 | |||||||
chr17:81197330 | C | T | 1 | a0003c0031t0007g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1648-275G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197330 | |||||||
chr17:81197358 | A | G | 123 | a0001c0003t0001g0264 a0001c0003t0001g0293 a0001c0003t0002g0006 others(120): Show |
140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1648-303T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197358 | |||||||
chr17:81197373 | C | T | 4 | a0016c0038t0001g0243 a0026c0072t0001g0303 a0036c0057t0001g0138 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648-318G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197373 | |||||||
chr17:81197380 | A | ACGGGTGG | 138 | a0001c0003t0001g0264 a0001c0003t0001g0293 a0001c0003t0002g0006 others(135): Show |
155 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1648-326_1648-325i others(9): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197380 | |||||||
chr17:81197454 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1647+258C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197454 | |||||||
chr17:81197497 | CA | C | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+214delT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197497 | |||||||
chr17:81197502 | T | A | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+210A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197502 | |||||||
chr17:81197504 | A | G | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+208T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197504 | |||||||
chr17:81197505 | G | T | 1 | a0037c0041t0001g0242 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1647+207C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197505 | |||||||
chr17:81197506 | A | G | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+206T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197506 | |||||||
chr17:81197508 | ACCCGTG | A | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+198_1647+203d others(8): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197508 | |||||||
chr17:81197517 | G | A | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+195C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197517 | |||||||
chr17:81197520 | TGCTGCAT others(68): Show |
T | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+117_1647+191d others(77): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197520 | |||||||
chr17:81197541 | C | T | 1 | a0039c0029t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1647+171G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197541 | |||||||
chr17:81197570 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1647+142G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197570 | |||||||
chr17:81197572 | G | A | 6 | a0003c0008t0003g0306 a0003c0008t0003g0307 a0003c0008t0003g0308 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1647+140C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197572 | |||||||
chr17:81197605 | G | GA | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+106_1647+107i others(3): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197605 | |||||||
chr17:81197608 | G | A | 2 | a0024c0035t0003g0312 a0040c0033t0003g0311 |
2 | HG01255.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1647+104C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197608 | |||||||
chr17:81197609 | C | G | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+103G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197609 | |||||||
chr17:81197611 | A | T | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+101T>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197611 | |||||||
chr17:81197616 | C | A | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+96G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197616 | |||||||
chr17:81197616 | C | T | 2 | a0024c0035t0003g0312 a0040c0033t0003g0311 |
2 | HG01255.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1647+96G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197616 | |||||||
chr17:81197619 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0210 |
3 | HG00408.hp2 NA18944.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1647+93C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197619 | |||||||
chr17:81197622 | G | C | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+90C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197622 | |||||||
chr17:81197623 | G | C | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+89C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197623 | |||||||
chr17:81197625 | G | C | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+87C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197625 | |||||||
chr17:81197626 | A | C | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+86T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197626 | |||||||
chr17:81197627 | G | C | 1 | a0044c0046t0002g0040 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1647+85C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197627 | |||||||
chr17:81197627 | G | T | 3 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 |
3 | HG02258.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1647+85C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197627 | |||||||
chr17:81197628 | G | T | 5 | a0002c0002t0001g0273 a0002c0002t0002g0038 a0002c0002t0002g0041 others(2): Show |
5 | NA18969.hp1 NA19009.hp1 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.1647+84C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 13/25 | chr17 | 81197628 | |||||||
chr17:81197998 | C | T | 10 | a0001c0001t0001g0239 a0001c0004t0001g0269 a0001c0004t0001g0288 others(7): Show |
11 | HG00438.hp1 HG04228.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1471-110G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 12/25 | chr17 | 81197998 | |||||||
chr17:81198005 | C | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
110 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1470+110G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 12/25 | chr17 | 81198005 | |||||||
chr17:81198029 | T | C | 3 | a0001c0018t0001g0180 a0001c0018t0001g0191 a0013c0017t0001g0187 |
3 | NA18947.hp1 NA18966.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1470+86A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 12/25 | chr17 | 81198029 | |||||||
chr17:81198319 | G | C | 12 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0028 others(9): Show |
14 | HG00323.hp2 HG00733.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1288-22C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/25 | chr17 | 81198319 | |||||||
chr17:81198372 | G | A | 1 | a0029c0067t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1288-75C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/25 | chr17 | 81198372 | |||||||
chr17:81198393 | G | A | 17 | a0001c0058t0003g0331 a0003c0014t0003g0314 a0003c0014t0003g0322 others(14): Show |
17 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1288-96C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/25 | chr17 | 81198393 | |||||||
chr17:81198458 | G | A | 4 | a0001c0003t0002g0070 a0001c0003t0002g0071 a0001c0003t0002g0072 others(1): Show |
4 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288-161C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/25 | chr17 | 81198458 | |||||||
chr17:81198560 | T | C | 324 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(321): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.1288-263A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/25 | chr17 | 81198560 | |||||||
chr17:81198672 | G | A | 2 | a0016c0040t0001g0244 a0016c0042t0001g0245 |
2 | HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1287+205C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/25 | chr17 | 81198672 | |||||||
chr17:81198744 | T | C | 10 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1287+133A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/25 | chr17 | 81198744 | |||||||
chr17:81198775 | C | T | 3 | a0001c0001t0001g0179 a0001c0018t0001g0180 a0001c0018t0001g0191 |
3 | NA18948.hp2 NA18966.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1287+102G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/25 | chr17 | 81198775 | |||||||
chr17:81198777 | G | C | 1 | a0001c0051t0002g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1287+100C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/25 | chr17 | 81198777 | |||||||
chr17:81198855 | T | C | 14 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(11): Show |
14 | HG01255.hp2 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1287+22A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 11/25 | chr17 | 81198855 | |||||||
chr17:81199129 | G | A | 1 | a0003c0031t0007g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1193-158C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 10/25 | chr17 | 81199129 | |||||||
chr17:81199270 | C | T | 1 | a0003c0008t0003g0317 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1192+111G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 10/25 | chr17 | 81199270 | |||||||
chr17:81199309 | C | T | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1192+72G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 10/25 | chr17 | 81199309 | |||||||
chr17:81199314 | A | G | 11 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(8): Show |
11 | HG01255.hp2 HG01891.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1192+67T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 10/25 | chr17 | 81199314 | |||||||
chr17:81199348 | C | T | 1 | a0012c0016t0001g0253 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1192+33G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 10/25 | chr17 | 81199348 | |||||||
chr17:81199578 | C | T | 9 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(6): Show |
9 | HG01891.hp2 HG02630.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1024-29G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 9/25 | chr17 | 81199578 | |||||||
chr17:81199598 | A | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(131): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1024-49T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 9/25 | chr17 | 81199598 | |||||||
chr17:81199620 | T | G | 1 | a0016c0042t0001g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1024-71A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 9/25 | chr17 | 81199620 | |||||||
chr17:81199623 | G | A | 1 | a0001c0012t0001g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1024-74C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 9/25 | chr17 | 81199623 | |||||||
chr17:81199639 | G | A | 8 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(5): Show |
8 | HG02630.hp1 HG02735.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+80C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 9/25 | chr17 | 81199639 | |||||||
chr17:81199662 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(113): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1023+57G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 9/25 | chr17 | 81199662 | |||||||
chr17:81199669 | G | A | 4 | a0001c0004t0001g0149 a0001c0004t0001g0302 a0001c0004t0002g0011 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.1023+50C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 9/25 | chr17 | 81199669 | |||||||
chr17:81199692 | G | A | 8 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(5): Show |
8 | HG02630.hp1 HG02735.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+27C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 9/25 | chr17 | 81199692 | |||||||
chr17:81199937 | G | A | 8 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(5): Show |
8 | HG01891.hp2 HG02572.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.907-102C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/25 | chr17 | 81199937 | |||||||
chr17:81199958 | G | A | 11 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0057 others(8): Show |
13 | HG01168.hp1 HG01169.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.907-123C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/25 | chr17 | 81199958 | |||||||
chr17:81200035 | C | T | 5 | a0001c0058t0003g0331 a0016c0038t0001g0243 a0016c0040t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.907-200G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/25 | chr17 | 81200035 | |||||||
chr17:81200119 | C | T | 1 | a0009c0011t0001g0018 | 2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.906+210G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/25 | chr17 | 81200119 | |||||||
chr17:81200120 | G | A | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.906+209C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/25 | chr17 | 81200120 | |||||||
chr17:81200156 | G | T | 1 | a0001c0001t0001g0205 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.906+173C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/25 | chr17 | 81200156 | |||||||
chr17:81200305 | A | C | 1 | a0001c0001t0001g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.906+24T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/25 | chr17 | 81200305 | |||||||
chr17:81200319 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.906+10G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/25 | chr17 | 81200319 | |||||||
chr17:81200326 | G | T | 1 | a0044c0046t0002g0040 | 1 | NA18977.hp2 | splice_region_variant&intron_variant | LOW | c.906+3C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 8/25 | chr17 | 81200326 | |||||||
chr17:81200459 | C | A | 15 | a0001c0003t0002g0118 a0001c0004t0002g0051 a0001c0004t0002g0053 others(12): Show |
15 | HG00639.hp1 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.789-13G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81200459 | |||||||
chr17:81200520 | G | A | 1 | a0032c0043t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.789-74C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81200520 | |||||||
chr17:81200527 | C | A | 5 | a0001c0001t0001g0188 a0001c0019t0001g0171 a0001c0019t0001g0189 others(2): Show |
5 | HG00741.hp2 HG01934.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.789-81G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81200527 | |||||||
chr17:81200548 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18971.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.789-102C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81200548 | |||||||
chr17:81200556 | T | A | 10 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.789-110A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81200556 | |||||||
chr17:81200669 | G | A | 1 | a0037c0041t0001g0242 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.789-223C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81200669 | |||||||
chr17:81200708 | T | A | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.789-262A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81200708 | |||||||
chr17:81200911 | T | A | 10 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.789-465A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81200911 | |||||||
chr17:81200916 | G | A | 1 | a0003c0014t0003g0324 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.789-470C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81200916 | |||||||
chr17:81200927 | T | A | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.789-481A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81200927 | |||||||
chr17:81200937 | C | G | 2 | a0026c0072t0001g0303 a0029c0067t0001g0126 |
2 | HG01891.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.789-491G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81200937 | |||||||
chr17:81201002 | G | C | 1 | a0018c0028t0001g0221 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.789-556C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201002 | |||||||
chr17:81201058 | T | A | 5 | a0001c0058t0003g0331 a0016c0038t0001g0243 a0016c0040t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.789-612A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201058 | |||||||
chr17:81201064 | A | C | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(313): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.789-618T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201064 | |||||||
chr17:81201224 | G | A | 1 | a0001c0003t0002g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.789-778C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201224 | |||||||
chr17:81201259 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.789-813C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201259 | |||||||
chr17:81201316 | C | T | 58 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0007 others(55): Show |
64 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.789-870G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201316 | |||||||
chr17:81201360 | C | T | 1 | a0002c0061t0001g0177 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.788+880G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201360 | |||||||
chr17:81201401 | C | T | 1 | a0029c0067t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.788+839G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201401 | |||||||
chr17:81201458 | C | A | 17 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(14): Show |
21 | HG01358.hp2 HG02080.hp1 HG02129.hp2 others(18): Show |
intron_variant | MODIFIER | c.788+782G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201458 | |||||||
chr17:81201486 | C | T | 1 | a0035c0048t0002g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.788+754G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201486 | |||||||
chr17:81201681 | T | A | 2 | a0032c0043t0001g0246 a0048c0034t0003g0305 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.788+559A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201681 | |||||||
chr17:81201840 | G | A | 1 | a0007c0009t0001g0262 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.788+400C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81201840 | |||||||
chr17:81202038 | T | C | 17 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(14): Show |
21 | HG01358.hp2 HG02080.hp1 HG02129.hp2 others(18): Show |
intron_variant | MODIFIER | c.788+202A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81202038 | |||||||
chr17:81202057 | C | T | 2 | a0001c0003t0002g0076 a0008c0010t0002g0106 |
2 | HG00323.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.788+183G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81202057 | |||||||
chr17:81202095 | T | C | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(313): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.788+145A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81202095 | |||||||
chr17:81202100 | C | CA | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(109): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.788+139dupT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81202100 | |||||||
chr17:81202210 | G | GC | 15 | a0001c0001t0001g0135 a0001c0001t0001g0232 a0001c0003t0002g0049 others(12): Show |
15 | HG00642.hp1 HG00673.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.788+29dupG | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81202210 | |||||||
chr17:81202212 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.788+28G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81202212 | |||||||
chr17:81202217 | C | G | 16 | a0001c0054t0001g0263 a0003c0008t0003g0306 a0003c0008t0003g0307 others(13): Show |
17 | HG01884.hp1 HG02109.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.788+23G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81202217 | |||||||
chr17:81202228 | A | G | 6 | a0011c0015t0006g0319 a0011c0015t0006g0320 a0011c0015t0006g0321 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.788+12T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81202228 | |||||||
chr17:81202232 | T | G | 11 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(8): Show |
11 | HG01255.hp2 HG01891.hp2 HG02572.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.788+8A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81202232 | |||||||
chr17:81202233 | C | T | 1 | a0011c0015t0006g0320 | 1 | HG01884.hp2 | splice_region_variant&intron_variant | LOW | c.788+7G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 7/25 | chr17 | 81202233 | |||||||
chr17:81202512 | G | T | 4 | a0001c0003t0002g0060 a0001c0003t0002g0067 a0001c0003t0002g0068 others(1): Show |
4 | HG01243.hp2 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-114C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202512 | |||||||
chr17:81202558 | C | T | 1 | a0007c0009t0001g0260 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.630-160G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202558 | |||||||
chr17:81202575 | A | T | 1 | a0012c0016t0001g0251 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.630-177T>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202575 | |||||||
chr17:81202628 | A | C | 1 | a0001c0003t0002g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.630-230T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202628 | |||||||
chr17:81202629 | G | A | 1 | a0001c0003t0002g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.630-231C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202629 | |||||||
chr17:81202741 | C | A | 9 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(6): Show |
9 | HG01891.hp2 HG02630.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.630-343G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202741 | |||||||
chr17:81202828 | G | A | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.630-430C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202828 | |||||||
chr17:81202864 | T | G | 9 | a0001c0054t0001g0263 a0003c0008t0003g0306 a0003c0008t0003g0307 others(6): Show |
10 | HG01884.hp1 HG02109.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.630-466A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202864 | |||||||
chr17:81202908 | A | G | 9 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(6): Show |
9 | HG01891.hp2 HG02630.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.630-510T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202908 | |||||||
chr17:81202964 | C | A | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.629+530G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202964 | |||||||
chr17:81202964 | CA | C | 9 | a0001c0001t0001g0160 a0001c0001t0001g0176 a0001c0001t0001g0204 others(6): Show |
9 | HG01074.hp2 HG01993.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.629+529delT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202964 | |||||||
chr17:81202978 | AT | A | 115 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0007 others(112): Show |
130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.629+515delA | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202978 | |||||||
chr17:81202979 | T | A | 1 | a0001c0003t0002g0012 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.629+515A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202979 | |||||||
chr17:81202984 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG00741.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.629+510A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81202984 | |||||||
chr17:81203063 | C | T | 5 | a0001c0003t0005g0121 a0001c0003t0005g0122 a0001c0003t0005g0123 others(2): Show |
5 | HG00099.hp1 HG00733.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.629+431G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81203063 | |||||||
chr17:81203143 | C | T | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.629+351G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81203143 | |||||||
chr17:81203165 | G | A | 2 | a0001c0004t0002g0075 a0002c0002t0002g0074 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.629+329C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81203165 | |||||||
chr17:81203258 | C | T | 1 | a0001c0058t0003g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.629+236G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81203258 | |||||||
chr17:81203260 | G | C | 1 | a0036c0057t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.629+234C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81203260 | |||||||
chr17:81203301 | G | A | 3 | a0002c0002t0002g0014 a0002c0002t0002g0015 a0002c0002t0002g0120 |
5 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.629+193C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81203301 | |||||||
chr17:81203353 | C | A | 8 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0188 others(5): Show |
8 | HG00558.hp2 HG00741.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.629+141G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81203353 | |||||||
chr17:81203359 | G | A | 2 | a0032c0043t0001g0246 a0048c0034t0003g0305 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.629+135C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81203359 | |||||||
chr17:81203407 | G | A | 9 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(6): Show |
9 | HG01891.hp2 HG02630.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.629+87C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 6/25 | chr17 | 81203407 | |||||||
chr17:81203773 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.516-166G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81203773 | |||||||
chr17:81203858 | C | T | 1 | a0001c0003t0002g0118 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.516-251G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81203858 | |||||||
chr17:81203860 | G | A | 1 | a0001c0058t0003g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.516-253C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81203860 | |||||||
chr17:81203874 | C | T | 1 | a0032c0043t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.516-267G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81203874 | |||||||
chr17:81203924 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0001g0230 |
2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.516-317A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81203924 | |||||||
chr17:81204025 | C | T | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.516-418G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204025 | |||||||
chr17:81204030 | C | T | 1 | a0012c0016t0001g0300 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.516-423G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204030 | |||||||
chr17:81204062 | G | C | 5 | a0001c0058t0003g0331 a0016c0038t0001g0243 a0016c0040t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.516-455C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204062 | |||||||
chr17:81204152 | G | A | 2 | a0032c0043t0001g0246 a0048c0034t0003g0305 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.516-545C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204152 | |||||||
chr17:81204174 | G | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(113): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.516-567C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204174 | |||||||
chr17:81204183 | C | G | 11 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(8): Show |
11 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-576G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204183 | |||||||
chr17:81204275 | C | T | 5 | a0001c0058t0003g0331 a0016c0038t0001g0243 a0016c0040t0001g0244 others(2): Show |
5 | HG02145.hp2 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.516-668G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204275 | |||||||
chr17:81204301 | G | A | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(248): Show |
291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.516-694C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204301 | |||||||
chr17:81204302 | C | T | 1 | a0004c0005t0001g0281 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.516-695G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204302 | |||||||
chr17:81204348 | C | T | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(247): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.516-741G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204348 | |||||||
chr17:81204349 | A | G | 314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(311): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.516-742T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204349 | |||||||
chr17:81204377 | G | A | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.516-770C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204377 | |||||||
chr17:81204391 | C | T | 1 | a0001c0004t0001g0289 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.516-784G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204391 | |||||||
chr17:81204396 | C | T | 118 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0007 others(115): Show |
134 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.516-789G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204396 | |||||||
chr17:81204460 | T | G | 10 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.516-853A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204460 | |||||||
chr17:81204631 | A | G | 10 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.516-1024T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204631 | |||||||
chr17:81204635 | T | C | 12 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(9): Show |
12 | HG01255.hp2 HG01891.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.516-1028A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204635 | |||||||
chr17:81204665 | A | C | 12 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(9): Show |
12 | HG01255.hp2 HG01891.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.516-1058T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204665 | |||||||
chr17:81204670 | C | T | 1 | a0001c0003t0001g0293 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.516-1063G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204670 | |||||||
chr17:81204704 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(113): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.516-1097G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204704 | |||||||
chr17:81204726 | GCACCTGC others(9): Show |
G | 11 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(8): Show |
11 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-1135_516-1120d others(18): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204726 | |||||||
chr17:81204752 | C | T | 1 | a0003c0008t0003g0316 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.516-1145G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204752 | |||||||
chr17:81204758 | A | G | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.516-1151T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204758 | |||||||
chr17:81204763 | T | A | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.516-1156A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204763 | |||||||
chr17:81204768 | C | T | 2 | a0013c0017t0001g0200 a0036c0057t0001g0138 |
2 | HG02132.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.516-1161G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204768 | |||||||
chr17:81204793 | G | A | 1 | a0042c0065t0001g0231 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.516-1186C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204793 | |||||||
chr17:81204866 | C | T | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.516-1259G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204866 | |||||||
chr17:81204889 | G | GT | 6 | a0001c0003t0002g0012 a0001c0003t0002g0048 a0001c0003t0002g0064 others(3): Show |
7 | HG01081.hp2 HG01109.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.516-1283dupA | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204889 | |||||||
chr17:81204956 | A | C | 11 | a0001c0054t0001g0263 a0003c0008t0003g0306 a0003c0008t0003g0307 others(8): Show |
12 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.516-1349T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204956 | |||||||
chr17:81204983 | G | A | 9 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(6): Show |
9 | HG01891.hp2 HG02572.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.516-1376C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81204983 | |||||||
chr17:81205056 | C | G | 11 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(8): Show |
11 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-1449G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205056 | |||||||
chr17:81205128 | A | G | 12 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(9): Show |
12 | HG01255.hp2 HG01891.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.516-1521T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205128 | |||||||
chr17:81205181 | C | G | 1 | a0001c0004t0001g0288 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.515+1563G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205181 | |||||||
chr17:81205225 | C | T | 1 | a0001c0062t0001g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.515+1519G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205225 | |||||||
chr17:81205336 | G | GGGGTAGG others(18): Show |
1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.515+1407_515+1408i others(27): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205336 | |||||||
chr17:81205336 | G | GGGGTAGG others(17): Show |
39 | a0001c0003t0001g0293 a0001c0004t0001g0025 a0001c0004t0001g0268 others(36): Show |
45 | HG00099.hp2 HG01358.hp2 HG01496.hp1 others(42): Show |
intron_variant | MODIFIER | c.515+1384_515+1407d others(26): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205336 | |||||||
chr17:81205349 | C | T | 11 | a0001c0054t0001g0263 a0003c0008t0003g0306 a0003c0008t0003g0307 others(8): Show |
12 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.515+1395G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205349 | |||||||
chr17:81205360 | T | TGGGTAGG others(13): Show |
1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.515+1364_515+1383d others(22): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205360 | |||||||
chr17:81205367 | G | A | 11 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(8): Show |
11 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.515+1377C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205367 | |||||||
chr17:81205396 | C | T | 8 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(5): Show |
8 | HG02273.hp2 HG02280.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.515+1348G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205396 | |||||||
chr17:81205414 | G | GTAGGAGG others(114): Show |
1 | a0039c0029t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.515+1329_515+1330i others(123): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205414 | |||||||
chr17:81205427 | C | T | 10 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.515+1317G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205427 | |||||||
chr17:81205431 | A | T | 10 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.515+1313T>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205431 | |||||||
chr17:81205432 | T | C | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.515+1312A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205432 | |||||||
chr17:81205432 | T | G | 10 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.515+1312A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205432 | |||||||
chr17:81205432 | TGGGGGTA others(10): Show |
T | 11 | a0001c0054t0001g0263 a0003c0008t0003g0306 a0003c0008t0003g0307 others(8): Show |
12 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.515+1295_515+1311d others(19): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205432 | |||||||
chr17:81205439 | A | AGGAGGGT others(9): Show |
1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.515+1304_515+1305i others(18): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205439 | |||||||
chr17:81205447 | T | C | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.515+1297A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205447 | |||||||
chr17:81205448 | G | A | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.515+1296C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205448 | |||||||
chr17:81205448 | G | GGGGGGGG others(11): Show |
1 | a0004c0005t0001g0274 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.515+1295_515+1296i others(20): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205448 | |||||||
chr17:81205448 | G | GGGGGGGT others(10): Show |
45 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(42): Show |
50 | HG00621.hp1 HG01074.hp2 HG01256.hp1 others(47): Show |
intron_variant | MODIFIER | c.515+1295_515+1296i others(19): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205448 | |||||||
chr17:81205450 | G | GT | 8 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(5): Show |
8 | HG01891.hp2 HG02572.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.515+1293_515+1294i others(3): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205450 | |||||||
chr17:81205462 | G | GGCAGTGG others(54): Show |
1 | a0029c0067t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.515+1281_515+1282i others(63): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205462 | |||||||
chr17:81205462 | G | GGCAGTGG others(52): Show |
1 | a0026c0072t0001g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.515+1281_515+1282i others(61): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205462 | |||||||
chr17:81205462 | G | GGCAGTGG others(53): Show |
5 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(2): Show |
5 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.515+1281_515+1282i others(62): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205462 | |||||||
chr17:81205462 | G | GGCAGTGG others(55): Show |
1 | a0010c0013t0004g0337 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.515+1281_515+1282i others(64): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205462 | |||||||
chr17:81205462 | G | GGTGGGTG others(72): Show |
1 | a0048c0034t0003g0305 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.515+1281_515+1282i others(81): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205462 | |||||||
chr17:81205462 | G | GGTGGGTG others(71): Show |
1 | a0032c0043t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.515+1281_515+1282i others(80): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205462 | |||||||
chr17:81205467 | C | A | 10 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.515+1277G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205467 | |||||||
chr17:81205469 | C | G | 10 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.515+1275G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205469 | |||||||
chr17:81205472 | GGGTAGGA others(17): Show |
G | 1 | a0030c0059t0001g0163 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.515+1248_515+1271d others(26): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205472 | |||||||
chr17:81205474 | G | A | 10 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.515+1270C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205474 | |||||||
chr17:81205487 | CG | C | 12 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(9): Show |
12 | HG01255.hp2 HG01891.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.515+1256delC | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205487 | |||||||
chr17:81205491 | AGGGGAGG others(16): Show |
A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(117): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.515+1230_515+1252d others(25): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205491 | |||||||
chr17:81205496 | A | G | 12 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(9): Show |
12 | HG01255.hp2 HG01891.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.515+1248T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205496 | |||||||
chr17:81205504 | G | A | 12 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(9): Show |
12 | HG01255.hp2 HG01891.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.515+1240C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205504 | |||||||
chr17:81205827 | A | G | 1 | a0002c0002t0002g0119 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.515+917T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205827 | |||||||
chr17:81205839 | C | A | 1 | a0021c0026t0003g0330 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.515+905G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205839 | |||||||
chr17:81205876 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.515+868C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205876 | |||||||
chr17:81205903 | T | A | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.515+841A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205903 | |||||||
chr17:81205948 | A | G | 295 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(292): Show |
339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.515+796T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81205948 | |||||||
chr17:81206012 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0135 a0001c0001t0001g0222 |
4 | HG02080.hp2 NA18956.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.515+732G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81206012 | |||||||
chr17:81206106 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.515+638G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81206106 | |||||||
chr17:81206150 | G | T | 7 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(4): Show |
7 | HG02280.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.515+594C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81206150 | |||||||
chr17:81206266 | G | C | 6 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.515+478C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81206266 | |||||||
chr17:81206475 | A | AG | 3 | a0001c0004t0001g0298 a0004c0005t0001g0274 a0006c0007t0001g0157 |
3 | HG00438.hp1 HG00673.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.515+268dupC | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81206475 | |||||||
chr17:81206522 | TC | T | 4 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 others(1): Show |
4 | HG02258.hp2 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.515+221delG | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81206522 | |||||||
chr17:81206545 | G | A | 1 | a0004c0005t0001g0277 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.515+199C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81206545 | |||||||
chr17:81206569 | C | G | 113 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0007 others(110): Show |
129 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.515+175G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81206569 | |||||||
chr17:81206719 | T | C | 10 | a0001c0054t0001g0263 a0003c0008t0003g0306 a0003c0008t0003g0307 others(7): Show |
11 | HG01884.hp1 HG02109.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.515+25A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81206719 | |||||||
chr17:81206739 | C | T | 6 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.515+5G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 5/25 | chr17 | 81206739 | |||||||
chr17:81206948 | G | A | 7 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(4): Show |
7 | HG02280.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-77C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 4/25 | chr17 | 81206948 | |||||||
chr17:81206975 | A | G | 295 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(292): Show |
339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.388-104T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 4/25 | chr17 | 81206975 | |||||||
chr17:81206984 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.388-113A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 4/25 | chr17 | 81206984 | |||||||
chr17:81207029 | G | A | 25 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(22): Show |
29 | HG01358.hp2 HG02080.hp1 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.387+96C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 4/25 | chr17 | 81207029 | |||||||
chr17:81207036 | C | T | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+89G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 4/25 | chr17 | 81207036 | |||||||
chr17:81207258 | G | A | 1 | a0001c0018t0001g0191 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.273-19C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207258 | |||||||
chr17:81207402 | G | A | 291 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(288): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.273-163C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207402 | |||||||
chr17:81207413 | T | C | 1 | a0038c0055t0009g0092 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.273-174A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207413 | |||||||
chr17:81207424 | G | A | 1 | a0048c0034t0003g0305 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.273-185C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207424 | |||||||
chr17:81207490 | CTT | C | 279 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(276): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.273-253_273-252del others(2): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207490 | |||||||
chr17:81207494 | T | A | 279 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(276): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.273-255A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207494 | |||||||
chr17:81207495 | T | A | 279 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(276): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.273-256A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207495 | |||||||
chr17:81207509 | C | CT | 10 | a0001c0058t0003g0331 a0003c0014t0003g0314 a0003c0014t0003g0322 others(7): Show |
10 | HG02145.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.273-271dupA | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207509 | |||||||
chr17:81207537 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.273-298A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207537 | |||||||
chr17:81207927 | A | ACCACACA others(1093): Show |
1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.273-689_273-688ins others(1100): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1079): Show |
1 | a0003c0031t0007g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.273-689_273-688ins others(1086): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1071): Show |
1 | a0001c0001t0001g0154 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.273-689_273-688ins others(1078): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1073): Show |
1 | a0018c0028t0001g0133 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.273-689_273-688ins others(1080): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1082): Show |
5 | a0011c0015t0006g0319 a0011c0015t0006g0320 a0011c0015t0006g0321 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1089): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1071): Show |
108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(105): Show |
130 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1078): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1071): Show |
1 | a0001c0001t0001g0198 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.273-689_273-688ins others(1078): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1071): Show |
3 | a0009c0011t0001g0018 a0009c0011t0001g0172 a0009c0011t0001g0224 |
4 | HG00140.hp1 HG00642.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1078): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1071): Show |
2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02698.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.273-689_273-688ins others(1078): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1069): Show |
1 | a0001c0001t0001g0192 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.273-689_273-688ins others(1076): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1147): Show |
1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.273-689_273-688ins others(1154): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1077): Show |
1 | a0005c0006t0001g0258 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.273-689_273-688ins others(1084): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1077): Show |
13 | a0001c0004t0002g0051 a0001c0004t0002g0053 a0001c0051t0002g0055 others(10): Show |
15 | HG00639.hp1 HG02055.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1084): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1000): Show |
2 | a0001c0004t0001g0271 a0001c0004t0001g0291 |
2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.273-689_273-688ins others(1007): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1086): Show |
37 | a0001c0003t0001g0293 a0001c0004t0001g0025 a0001c0004t0001g0268 others(34): Show |
40 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1093): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1086): Show |
1 | a0001c0004t0001g0292 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.273-689_273-688ins others(1093): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1084): Show |
1 | a0004c0044t0011g0297 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.273-689_273-688ins others(1091): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1084): Show |
75 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0012 others(72): Show |
87 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1091): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1028): Show |
4 | a0001c0058t0003g0331 a0016c0040t0001g0244 a0016c0042t0001g0245 others(1): Show |
4 | HG02145.hp2 HG02895.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1035): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1075): Show |
1 | a0001c0003t0002g0118 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.273-689_273-688ins others(1082): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1084): Show |
7 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(4): Show |
7 | HG02280.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1091): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1084): Show |
1 | a0036c0057t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.273-689_273-688ins others(1091): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1084): Show |
13 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0255 others(10): Show |
17 | HG01358.hp2 HG02129.hp2 NA18940.hp1 others(14): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1091): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1075): Show |
3 | a0002c0002t0012g0304 a0003c0023t0003g0326 a0003c0023t0003g0327 |
3 | HG02055.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.273-689_273-688ins others(1082): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1082): Show |
1 | a0002c0002t0002g0116 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.273-689_273-688ins others(1089): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1073): Show |
1 | a0034c0032t0003g0315 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.273-689_273-688ins others(1080): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1082): Show |
12 | a0001c0054t0001g0263 a0003c0008t0003g0306 a0003c0008t0003g0307 others(9): Show |
13 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1089): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1098): Show |
17 | a0001c0003t0002g0007 a0001c0003t0002g0049 a0001c0003t0002g0081 others(14): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1105): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1082): Show |
2 | a0001c0003t0002g0057 a0008c0050t0002g0058 |
2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273-689_273-688ins others(1089): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1087): Show |
1 | a0029c0067t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.273-689_273-688ins others(1094): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1091): Show |
1 | a0039c0029t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.273-689_273-688ins others(1098): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1091): Show |
5 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1098): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1086): Show |
1 | a0048c0034t0003g0305 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.273-689_273-688ins others(1093): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1089): Show |
1 | a0032c0043t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.273-689_273-688ins others(1096): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1093): Show |
6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.273-689_273-688ins others(1100): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACA others(1084): Show |
1 | a0002c0002t0002g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.273-689_273-688ins others(1091): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207927 | A | ACCACACC others(1082): Show |
1 | a0002c0002t0002g0109 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.273-689_273-688ins others(1089): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207927 | |||||||
chr17:81207935 | C | CCATACAC others(1083): Show |
1 | a0005c0006t0001g0256 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.273-697_273-696ins others(1090): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207935 | |||||||
chr17:81207956 | TAC | T | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.273-719_273-718del others(2): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81207956 | |||||||
chr17:81208003 | ACACACAC others(17): Show |
A | 1 | a0001c0003t0002g0089 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.273-788_273-765del others(24): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208003 | |||||||
chr17:81208034 | C | A | 1 | a0001c0003t0002g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.273-795G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208034 | |||||||
chr17:81208047 | A | C | 7 | a0001c0003t0002g0028 a0001c0058t0003g0331 a0016c0038t0001g0243 others(4): Show |
7 | HG01255.hp2 HG01346.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.273-808T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208047 | |||||||
chr17:81208083 | CACCACAC others(38): Show |
C | 1 | a0003c0014t0003g0325 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.272+800_272+844del others(45): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208083 | |||||||
chr17:81208100 | T | C | 15 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(12): Show |
15 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.272+828A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208100 | |||||||
chr17:81208213 | C | G | 1 | a0039c0029t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.272+715G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208213 | |||||||
chr17:81208261 | C | T | 3 | a0002c0002t0002g0097 a0002c0002t0002g0112 a0008c0010t0002g0098 |
3 | NA18949.hp1 NA18957.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.272+667G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208261 | |||||||
chr17:81208345 | C | T | 2 | a0002c0002t0002g0036 a0044c0046t0002g0040 |
2 | NA18962.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.272+583G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208345 | |||||||
chr17:81208454 | C | A | 5 | a0001c0001t0001g0194 a0016c0038t0001g0243 a0016c0040t0001g0244 others(2): Show |
5 | HG02895.hp2 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.272+474G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208454 | |||||||
chr17:81208491 | C | T | 24 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(21): Show |
28 | HG01358.hp2 HG02129.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.272+437G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208491 | |||||||
chr17:81208506 | C | T | 1 | a0004c0045t0001g0280 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.272+422G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208506 | |||||||
chr17:81208507 | G | T | 5 | a0011c0015t0006g0319 a0011c0015t0006g0320 a0011c0015t0006g0321 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.272+421C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208507 | |||||||
chr17:81208626 | G | A | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.272+302C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208626 | |||||||
chr17:81208647 | G | A | 1 | a0048c0034t0003g0305 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.272+281C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208647 | |||||||
chr17:81208747 | G | A | 3 | a0004c0005t0001g0278 a0004c0005t0001g0296 a0007c0009t0001g0279 |
3 | HG01256.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.272+181C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208747 | |||||||
chr17:81208771 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.272+157A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208771 | |||||||
chr17:81208781 | G | A | 1 | a0001c0003t0002g0118 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.272+147C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208781 | |||||||
chr17:81208831 | G | C | 1 | a0001c0004t0002g0115 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.272+97C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208831 | |||||||
chr17:81208867 | A | G | 294 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(291): Show |
338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.272+61T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 3/25 | chr17 | 81208867 | |||||||
chr17:81209026 | C | T | 15 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(12): Show |
15 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.178-4G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209026 | |||||||
chr17:81209027 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG03017.hp1 | splice_region_variant&intron_variant | LOW | c.178-5T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209027 | |||||||
chr17:81209040 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.178-18T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209040 | |||||||
chr17:81209100 | G | A | 1 | a0029c0067t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.178-78C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209100 | |||||||
chr17:81209130 | C | T | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-108G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209130 | |||||||
chr17:81209185 | G | A | 1 | a0002c0002t0002g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.178-163C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209185 | |||||||
chr17:81209227 | G | A | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-205C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209227 | |||||||
chr17:81209339 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.178-317C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209339 | |||||||
chr17:81209348 | T | A | 2 | a0032c0043t0001g0246 a0048c0034t0003g0305 |
2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.178-326A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209348 | |||||||
chr17:81209367 | T | C | 7 | a0008c0010t0001g0272 a0010c0013t0004g0333 a0010c0013t0004g0334 others(4): Show |
7 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-345A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209367 | |||||||
chr17:81209461 | A | C | 16 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(13): Show |
16 | HG01255.hp2 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-439T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209461 | |||||||
chr17:81209475 | A | C | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-453T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209475 | |||||||
chr17:81209509 | G | T | 3 | a0001c0004t0001g0285 a0001c0004t0001g0298 a0002c0002t0001g0273 |
3 | HG00673.hp2 NA19060.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.178-487C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209509 | |||||||
chr17:81209532 | T | G | 24 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(21): Show |
28 | HG01358.hp2 HG02129.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.178-510A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209532 | |||||||
chr17:81209551 | CAG | C | 11 | a0001c0054t0001g0263 a0003c0008t0003g0306 a0003c0008t0003g0307 others(8): Show |
12 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.178-531_178-530del others(2): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209551 | |||||||
chr17:81209556 | ACTAAGCA others(28): Show |
A | 1 | a0002c0002t0001g0273 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.178-569_178-535del others(35): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209556 | |||||||
chr17:81209556 | ACTAAGCA others(343): Show |
A | 3 | a0011c0015t0006g0319 a0011c0015t0006g0320 a0038c0055t0009g0092 |
3 | HG01884.hp2 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.178-884_178-535del | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209556 | |||||||
chr17:81209556 | ACTAAGCA others(378): Show |
A | 3 | a0001c0001t0001g0141 a0011c0015t0006g0321 a0011c0015t0006g0323 |
3 | HG01167.hp2 HG01169.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.178-919_178-535del | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209556 | |||||||
chr17:81209563 | A | AAGGATCA others(28): Show |
21 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(18): Show |
25 | HG01358.hp2 HG02129.hp2 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.178-576_178-542dup others(35): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209563 | |||||||
chr17:81209563 | A | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(244): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.178-541T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209563 | |||||||
chr17:81209608 | GCGCTCGG others(133): Show |
G | 1 | a0008c0010t0001g0272 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.178-726_178-587del | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209608 | |||||||
chr17:81209643 | GCGCTCGG others(98): Show |
G | 26 | a0001c0004t0001g0025 a0001c0004t0001g0268 a0001c0004t0001g0269 others(23): Show |
28 | HG00099.hp2 HG00673.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.178-726_178-622del | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209643 | |||||||
chr17:81209649 | GGAGAAGC others(238): Show |
G | 10 | a0001c0001t0001g0162 a0001c0001t0001g0170 a0001c0019t0001g0171 others(7): Show |
10 | HG00735.hp1 HG01934.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.178-872_178-628del | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209649 | |||||||
chr17:81209678 | GCGCTCGG others(308): Show |
G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0135 a0001c0001t0001g0194 others(9): Show |
16 | HG01070.hp2 HG01071.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.178-971_178-657del | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209678 | |||||||
chr17:81209684 | GGAGAAGC others(203): Show |
G | 23 | a0001c0003t0002g0060 a0001c0004t0001g0282 a0001c0004t0001g0291 others(20): Show |
24 | HG01255.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.178-872_178-663del | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209684 | |||||||
chr17:81209713 | G | GCGCTCGG others(63): Show |
1 | a0003c0014t0003g0325 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.178-692_178-691ins others(70): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209713 | |||||||
chr17:81209713 | GCGCTCGG others(273): Show |
G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(96): Show |
116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.178-971_178-692del | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209713 | |||||||
chr17:81209719 | GGAGAAGC others(168): Show |
G | 10 | a0001c0003t0002g0057 a0004c0005t0001g0023 a0004c0005t0001g0274 others(7): Show |
11 | HG00438.hp1 HG00621.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-872_178-698del | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209719 | |||||||
chr17:81209737 | C | CGAGGATC others(29): Show |
1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-716_178-715ins others(36): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209737 | |||||||
chr17:81209748 | C | G | 126 | a0001c0001t0001g0017 a0001c0001t0001g0168 a0001c0001t0001g0169 others(123): Show |
143 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.178-726G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209748 | |||||||
chr17:81209772 | C | T | 2 | a0001c0004t0002g0075 a0002c0002t0002g0074 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.178-750G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209772 | |||||||
chr17:81209783 | G | C | 23 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(20): Show |
27 | HG01358.hp2 HG02129.hp2 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.178-761C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209783 | |||||||
chr17:81209789 | GGAGAAGC others(98): Show |
G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0168 a0001c0001t0001g0169 others(6): Show |
10 | HG01943.hp2 HG02040.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.178-872_178-768del | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209789 | |||||||
chr17:81209818 | G | C | 1 | a0036c0057t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.178-796C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209818 | |||||||
chr17:81209824 | GGAGAAGC others(63): Show |
G | 1 | a0001c0004t0002g0107 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.178-872_178-803del others(70): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209824 | |||||||
chr17:81209853 | G | C | 7 | a0001c0003t0002g0105 a0001c0003t0002g0108 a0001c0004t0002g0039 others(4): Show |
7 | HG00642.hp1 HG01243.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-831C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209853 | |||||||
chr17:81209853 | GCGCTCGG others(133): Show |
G | 19 | a0001c0003t0002g0006 a0001c0003t0002g0012 a0001c0003t0002g0013 others(16): Show |
23 | HG00323.hp2 HG01081.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.178-971_178-832del | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209853 | |||||||
chr17:81209859 | GGAGAAGC others(28): Show |
G | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-872_178-838del others(35): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209859 | |||||||
chr17:81209888 | C | CCGCTCGG others(28): Show |
15 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0255 others(12): Show |
19 | HG01358.hp2 HG02129.hp2 NA18940.hp1 others(16): Show |
intron_variant | MODIFIER | c.178-867_178-866ins others(35): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209888 | |||||||
chr17:81209888 | C | G | 3 | a0001c0003t0002g0028 a0001c0003t0002g0029 a0003c0014t0003g0325 |
3 | HG01167.hp1 HG01346.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.178-866G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209888 | |||||||
chr17:81209888 | CCGCTCCG others(168): Show |
C | 81 | a0001c0003t0001g0264 a0001c0003t0002g0007 a0001c0003t0002g0037 others(78): Show |
93 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.178-1041_178-867de others(1): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209888 | |||||||
chr17:81209888 | CCGCTCCG others(203): Show |
C | 7 | a0001c0003t0002g0105 a0001c0003t0002g0108 a0001c0004t0002g0039 others(4): Show |
7 | HG00642.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1076_178-867de others(1): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209888 | |||||||
chr17:81209894 | C | G | 25 | a0001c0003t0002g0028 a0001c0003t0002g0029 a0003c0014t0003g0314 others(22): Show |
29 | HG01167.hp1 HG01346.hp1 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.178-872G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209894 | |||||||
chr17:81209958 | G | C | 8 | a0003c0014t0003g0325 a0004c0005t0001g0023 a0004c0005t0001g0274 others(5): Show |
9 | HG00438.hp1 HG00621.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-936C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209958 | |||||||
chr17:81209958 | G | GCGCTCGG others(28): Show |
6 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-971_178-937dup others(35): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209958 | |||||||
chr17:81209964 | G | C | 7 | a0004c0005t0001g0023 a0004c0005t0001g0274 a0004c0005t0001g0275 others(4): Show |
8 | HG00438.hp1 HG00621.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.178-942C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209964 | |||||||
chr17:81209993 | C | G | 58 | a0001c0001t0001g0141 a0001c0001t0001g0162 a0001c0001t0001g0170 others(55): Show |
60 | HG00438.hp1 HG00621.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.178-971G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209993 | |||||||
chr17:81209999 | G | C | 1 | a0001c0004t0001g0291 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.178-977C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81209999 | |||||||
chr17:81210008 | G | GACGCTAA others(30): Show |
1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-987_178-986ins others(37): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210008 | |||||||
chr17:81210063 | G | C | 25 | a0001c0003t0002g0006 a0001c0003t0002g0012 a0001c0003t0002g0013 others(22): Show |
29 | HG00323.hp2 HG00735.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.178-1041C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210063 | |||||||
chr17:81210063 | G | GCGCTCGG others(28): Show |
1 | a0001c0003t0002g0028 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.178-1042_178-1041i others(37): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210063 | |||||||
chr17:81210098 | G | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(224): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.178-1076C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210098 | |||||||
chr17:81210111 | T | C | 1 | a0020c0056t0001g0148 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.178-1089A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210111 | |||||||
chr17:81210122 | G | GAAGTGGC others(8): Show |
25 | a0001c0054t0001g0263 a0003c0008t0003g0306 a0003c0008t0003g0307 others(22): Show |
26 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.178-1115_178-1101d others(17): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210122 | |||||||
chr17:81210231 | G | A | 5 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-1209C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210231 | |||||||
chr17:81210233 | A | T | 5 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-1211T>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210233 | |||||||
chr17:81210271 | C | G | 8 | a0001c0001t0001g0139 a0001c0001t0001g0162 a0001c0001t0001g0164 others(5): Show |
8 | HG00741.hp1 HG01928.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-1249G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210271 | |||||||
chr17:81210431 | A | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(114): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.178-1409T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210431 | |||||||
chr17:81210518 | C | T | 6 | a0001c0003t0002g0012 a0001c0003t0002g0048 a0001c0003t0002g0064 others(3): Show |
7 | HG01081.hp2 HG01109.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-1496G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210518 | |||||||
chr17:81210534 | C | T | 1 | a0003c0031t0007g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.178-1512G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210534 | |||||||
chr17:81210555 | C | T | 6 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-1533G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210555 | |||||||
chr17:81210567 | A | AAAAAAC | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0032c0043t0001g0246 |
3 | HG02630.hp1 HG02698.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.178-1551_178-1546d others(8): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210567 | |||||||
chr17:81210641 | T | G | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-1619A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210641 | |||||||
chr17:81210753 | A | G | 2 | a0001c0003t0002g0037 a0002c0047t0002g0034 |
2 | HG01993.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.178-1731T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210753 | |||||||
chr17:81210829 | C | A | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-1807G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210829 | |||||||
chr17:81210829 | C | CA | 120 | a0001c0001t0001g0207 a0001c0003t0001g0264 a0001c0003t0002g0006 others(117): Show |
137 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.178-1808dupT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210829 | |||||||
chr17:81210829 | C | CAA | 18 | a0001c0003t0005g0124 a0001c0058t0003g0331 a0002c0002t0012g0304 others(15): Show |
18 | HG01517.hp1 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.178-1809_178-1808d others(4): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210829 | |||||||
chr17:81210829 | C | CAAA | 16 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0255 others(13): Show |
20 | HG01358.hp2 HG02129.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.178-1810_178-1808d others(5): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210829 | |||||||
chr17:81210829 | CA | C | 6 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0001g0160 others(3): Show |
6 | HG01255.hp2 NA18612.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.178-1808delT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210829 | |||||||
chr17:81210895 | A | G | 8 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 others(5): Show |
8 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-1873T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210895 | |||||||
chr17:81210930 | G | A | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-1908C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210930 | |||||||
chr17:81210973 | C | A | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-1951G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210973 | |||||||
chr17:81210977 | G | A | 5 | a0011c0015t0006g0319 a0011c0015t0006g0320 a0011c0015t0006g0321 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-1955C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210977 | |||||||
chr17:81210984 | G | C | 33 | a0001c0054t0001g0263 a0001c0058t0003g0331 a0003c0008t0003g0306 others(30): Show |
38 | HG01358.hp2 HG01884.hp1 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.178-1962C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81210984 | |||||||
chr17:81211014 | A | G | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-1992T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211014 | |||||||
chr17:81211018 | T | C | 146 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0007 others(143): Show |
166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.178-1996A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211018 | |||||||
chr17:81211019 | G | A | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-1997C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211019 | |||||||
chr17:81211046 | C | T | 293 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(290): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.178-2024G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211046 | |||||||
chr17:81211106 | C | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0136 others(8): Show |
14 | HG00639.hp2 HG01981.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.178-2084G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211106 | |||||||
chr17:81211143 | AAC | A | 7 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(4): Show |
7 | HG02280.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.178-2123_178-2122d others(4): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211143 | |||||||
chr17:81211221 | T | C | 16 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(13): Show |
20 | HG01358.hp2 HG02129.hp2 NA18940.hp1 others(17): Show |
intron_variant | MODIFIER | c.178-2199A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211221 | |||||||
chr17:81211302 | C | T | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-2280G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211302 | |||||||
chr17:81211352 | G | A | 294 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(291): Show |
338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.178-2330C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211352 | |||||||
chr17:81211386 | C | T | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-2364G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211386 | |||||||
chr17:81211408 | A | G | 120 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0007 others(117): Show |
136 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.178-2386T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211408 | |||||||
chr17:81211504 | C | T | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-2482G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211504 | |||||||
chr17:81211512 | G | C | 4 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-2490C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211512 | |||||||
chr17:81211528 | C | T | 3 | a0001c0003t0002g0049 a0001c0003t0002g0084 a0001c0003t0002g0108 |
3 | HG00642.hp1 HG01934.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.178-2506G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211528 | |||||||
chr17:81211594 | G | A | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-2572C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211594 | |||||||
chr17:81211598 | C | A | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-2576G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211598 | |||||||
chr17:81211613 | G | C | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-2591C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211613 | |||||||
chr17:81211614 | C | T | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-2592G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211614 | |||||||
chr17:81211641 | C | T | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-2619G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211641 | |||||||
chr17:81211794 | G | A | 8 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0209 others(5): Show |
8 | HG00140.hp2 HG00280.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-2772C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211794 | |||||||
chr17:81211809 | T | A | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-2787A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211809 | |||||||
chr17:81211889 | T | C | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-2867A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211889 | |||||||
chr17:81211934 | G | GA | 63 | a0001c0001t0001g0232 a0001c0003t0001g0264 a0001c0003t0002g0006 others(60): Show |
69 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.178-2913dupT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211934 | |||||||
chr17:81211934 | GA | G | 26 | a0002c0002t0002g0111 a0003c0014t0003g0314 a0003c0014t0003g0322 others(23): Show |
30 | HG01358.hp2 HG02129.hp2 HG02280.hp2 others(27): Show |
intron_variant | MODIFIER | c.178-2913delT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211934 | |||||||
chr17:81211950 | G | A | 11 | a0001c0001t0001g0019 a0001c0054t0001g0263 a0003c0008t0003g0306 others(8): Show |
12 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.178-2928C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81211950 | |||||||
chr17:81212090 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0215 others(1): Show |
7 | HG02071.hp1 HG02129.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.178-3068C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212090 | |||||||
chr17:81212160 | T | C | 1 | a0042c0065t0001g0231 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.178-3138A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212160 | |||||||
chr17:81212259 | T | C | 1 | a0001c0012t0001g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.178-3237A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212259 | |||||||
chr17:81212305 | G | C | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-3283C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212305 | |||||||
chr17:81212321 | C | CA | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(225): Show |
271 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.178-3300dupT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212321 | |||||||
chr17:81212321 | C | CAA | 6 | a0001c0001t0001g0232 a0001c0003t0002g0081 a0001c0003t0002g0082 others(3): Show |
6 | HG01261.hp2 HG02257.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.178-3301_178-3300d others(4): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212321 | |||||||
chr17:81212328 | A | G | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-3306T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212328 | |||||||
chr17:81212332 | A | G | 11 | a0001c0054t0001g0263 a0003c0008t0003g0306 a0003c0008t0003g0307 others(8): Show |
12 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.178-3310T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212332 | |||||||
chr17:81212528 | CTGGGCAG others(38): Show |
C | 1 | a0001c0004t0002g0045 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.178-3551_178-3507d others(47): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212528 | |||||||
chr17:81212546 | T | TGTGCAGA others(38): Show |
1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-3569_178-3525d others(47): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212546 | |||||||
chr17:81212572 | C | T | 3 | a0004c0005t0001g0278 a0004c0005t0001g0296 a0007c0009t0001g0279 |
3 | HG01256.hp1 HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.178-3550G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212572 | |||||||
chr17:81212592 | G | A | 1 | a0002c0002t0002g0046 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.178-3570C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212592 | |||||||
chr17:81212648 | G | A | 1 | a0003c0008t0003g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.178-3626C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212648 | |||||||
chr17:81212708 | AGGGACAG others(8): Show |
A | 1 | a0036c0057t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.178-3701_178-3687d others(17): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212708 | |||||||
chr17:81212723 | T | C | 1 | a0001c0003t0002g0007 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.178-3701A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212723 | |||||||
chr17:81212747 | G | A | 1 | a0001c0003t0002g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.178-3725C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212747 | |||||||
chr17:81212770 | T | TG | 4 | a0001c0003t0002g0049 a0001c0003t0002g0084 a0001c0003t0002g0085 others(1): Show |
4 | HG00735.hp2 HG01934.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.178-3749_178-3748i others(3): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212770 | |||||||
chr17:81212771 | C | G | 293 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(290): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.178-3749G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212771 | |||||||
chr17:81212817 | C | T | 1 | a0011c0015t0006g0319 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.178-3795G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212817 | |||||||
chr17:81212884 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.178-3862C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212884 | |||||||
chr17:81212937 | T | C | 114 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0007 others(111): Show |
130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.178-3915A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81212937 | |||||||
chr17:81213106 | A | C | 1 | a0008c0010t0002g0106 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.178-4084T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213106 | |||||||
chr17:81213202 | T | C | 1 | a0001c0054t0001g0263 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.178-4180A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213202 | |||||||
chr17:81213303 | T | C | 4 | a0014c0021t0002g0063 a0014c0021t0002g0079 a0014c0021t0002g0080 others(1): Show |
4 | HG01070.hp1 HG01074.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-4281A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213303 | |||||||
chr17:81213311 | G | T | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(265): Show |
308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.178-4289C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213311 | |||||||
chr17:81213374 | A | T | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-4352T>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213374 | |||||||
chr17:81213382 | A | G | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-4360T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213382 | |||||||
chr17:81213385 | C | A | 1 | a0005c0006t0001g0248 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.178-4363G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213385 | |||||||
chr17:81213558 | C | CA | 116 | a0001c0001t0001g0218 a0001c0001t0001g0233 a0001c0001t0001g0239 others(113): Show |
130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.178-4537dupT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213558 | |||||||
chr17:81213558 | C | CAA | 8 | a0002c0002t0002g0047 a0005c0006t0001g0248 a0010c0013t0004g0333 others(5): Show |
8 | HG02965.hp1 HG03239.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-4538_178-4537d others(4): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213558 | |||||||
chr17:81213558 | C | CAAA | 14 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0255 others(11): Show |
18 | HG01358.hp2 HG02129.hp2 NA18940.hp1 others(15): Show |
intron_variant | MODIFIER | c.178-4539_178-4537d others(5): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213558 | |||||||
chr17:81213632 | T | C | 175 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0007 others(172): Show |
196 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.178-4610A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213632 | |||||||
chr17:81213684 | G | A | 1 | a0001c0003t0001g0293 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.178-4662C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213684 | |||||||
chr17:81213757 | C | T | 1 | a0001c0004t0001g0302 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.178-4735G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213757 | |||||||
chr17:81213806 | A | T | 1 | a0001c0058t0003g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.178-4784T>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213806 | |||||||
chr17:81213920 | G | T | 24 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(21): Show |
28 | HG01255.hp2 HG01358.hp2 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.178-4898C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81213920 | |||||||
chr17:81214021 | G | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0018t0001g0214 |
3 | HG00558.hp2 HG02015.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.178-4999C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214021 | |||||||
chr17:81214027 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.178-5005C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214027 | |||||||
chr17:81214113 | A | AT | 25 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(22): Show |
29 | HG01255.hp2 HG01358.hp2 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.178-5092dupA | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214113 | |||||||
chr17:81214162 | A | G | 12 | a0001c0054t0001g0263 a0003c0008t0003g0306 a0003c0008t0003g0307 others(9): Show |
13 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.178-5140T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214162 | |||||||
chr17:81214176 | G | C | 2 | a0032c0043t0001g0246 a0036c0057t0001g0138 |
2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.178-5154C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214176 | |||||||
chr17:81214186 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.178-5164C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214186 | |||||||
chr17:81214225 | T | C | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178-5203A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214225 | |||||||
chr17:81214413 | C | A | 3 | a0003c0023t0003g0326 a0003c0023t0003g0327 a0034c0032t0003g0315 |
3 | HG02055.hp2 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.178-5391G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214413 | |||||||
chr17:81214413 | C | G | 167 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0007 others(164): Show |
188 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.178-5391G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214413 | |||||||
chr17:81214481 | A | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(313): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.177+5399T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214481 | |||||||
chr17:81214503 | G | C | 176 | a0001c0001t0001g0195 a0001c0003t0001g0264 a0001c0003t0002g0006 others(173): Show |
197 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.177+5377C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214503 | |||||||
chr17:81214512 | C | T | 3 | a0001c0003t0002g0081 a0001c0003t0002g0082 a0001c0003t0002g0086 |
3 | HG01261.hp2 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.177+5368G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214512 | |||||||
chr17:81214556 | C | CA | 113 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0007 others(110): Show |
129 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.177+5323dupT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214556 | |||||||
chr17:81214626 | T | G | 1 | a0039c0029t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.177+5254A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214626 | |||||||
chr17:81214641 | T | A | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(289): Show |
336 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.177+5239A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214641 | |||||||
chr17:81214669 | G | A | 7 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(4): Show |
7 | HG02280.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+5211C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214669 | |||||||
chr17:81214771 | CA | C | 7 | a0001c0001t0001g0152 a0015c0022t0001g0129 a0015c0022t0001g0130 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+5108delT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214771 | |||||||
chr17:81214782 | A | T | 1 | a0002c0002t0002g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.177+5098T>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214782 | |||||||
chr17:81214783 | T | A | 1 | a0039c0029t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.177+5097A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214783 | |||||||
chr17:81214783 | T | C | 1 | a0032c0043t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.177+5097A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214783 | |||||||
chr17:81214819 | G | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(120): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.177+5061C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214819 | |||||||
chr17:81214833 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(119): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.177+5047G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214833 | |||||||
chr17:81214855 | T | C | 1 | a0029c0067t0001g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.177+5025A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214855 | |||||||
chr17:81214921 | T | C | 7 | a0002c0002t0001g0024 a0011c0015t0006g0319 a0011c0015t0006g0320 others(4): Show |
8 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.177+4959A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214921 | |||||||
chr17:81214929 | C | T | 286 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(283): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.177+4951G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214929 | |||||||
chr17:81214930 | G | A | 5 | a0011c0015t0006g0319 a0011c0015t0006g0320 a0011c0015t0006g0321 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+4950C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81214930 | |||||||
chr17:81215047 | G | A | 1 | a0032c0043t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.177+4833C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215047 | |||||||
chr17:81215067 | G | A | 1 | a0036c0057t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.177+4813C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215067 | |||||||
chr17:81215068 | C | T | 25 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(22): Show |
29 | HG01255.hp2 HG01358.hp2 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.177+4812G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215068 | |||||||
chr17:81215114 | G | C | 1 | a0004c0045t0001g0280 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.177+4766C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215114 | |||||||
chr17:81215168 | A | C | 1 | a0002c0002t0002g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.177+4712T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215168 | |||||||
chr17:81215191 | T | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(289): Show |
336 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.177+4689A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215191 | |||||||
chr17:81215236 | A | G | 16 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(13): Show |
20 | HG01358.hp2 HG02129.hp2 NA18940.hp1 others(17): Show |
intron_variant | MODIFIER | c.177+4644T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215236 | |||||||
chr17:81215293 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0210 others(1): Show |
4 | HG00408.hp2 HG00423.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+4587G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215293 | |||||||
chr17:81215378 | T | G | 1 | a0003c0014t0003g0325 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.177+4502A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215378 | |||||||
chr17:81215445 | G | A | 2 | a0029c0067t0001g0126 a0039c0029t0001g0301 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.177+4435C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215445 | |||||||
chr17:81215540 | T | C | 2 | a0001c0012t0001g0146 a0001c0012t0001g0147 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.177+4340A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215540 | |||||||
chr17:81215628 | TC | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(258): Show |
301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.177+4251delG | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215628 | |||||||
chr17:81215631 | C | T | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.177+4249G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215631 | |||||||
chr17:81215782 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG00673.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.177+4098C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215782 | |||||||
chr17:81215969 | T | A | 1 | a0001c0019t0001g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.177+3911A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81215969 | |||||||
chr17:81216002 | G | A | 11 | a0003c0008t0003g0306 a0003c0008t0003g0307 a0003c0008t0003g0308 others(8): Show |
12 | HG01884.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+3878C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216002 | |||||||
chr17:81216004 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(114): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.177+3876A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216004 | |||||||
chr17:81216005 | C | T | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(289): Show |
336 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.177+3875G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216005 | |||||||
chr17:81216047 | C | T | 1 | a0001c0004t0002g0107 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.177+3833G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216047 | |||||||
chr17:81216048 | CT | C | 16 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(13): Show |
20 | HG01358.hp2 HG02129.hp2 NA18940.hp1 others(17): Show |
intron_variant | MODIFIER | c.177+3831delA | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216048 | |||||||
chr17:81216177 | T | C | 1 | a0036c0057t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.177+3703A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216177 | |||||||
chr17:81216285 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01168.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.177+3595C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216285 | |||||||
chr17:81216526 | G | A | 2 | a0001c0004t0001g0282 a0032c0043t0001g0246 |
2 | HG02015.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.177+3354C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216526 | |||||||
chr17:81216661 | T | C | 326 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(323): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.177+3219A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216661 | |||||||
chr17:81216689 | G | A | 1 | a0039c0029t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.177+3191C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216689 | |||||||
chr17:81216690 | G | T | 1 | a0039c0029t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.177+3190C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216690 | |||||||
chr17:81216762 | A | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(260): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.177+3118T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216762 | |||||||
chr17:81216849 | C | G | 30 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(27): Show |
34 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.177+3031G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216849 | |||||||
chr17:81216860 | G | T | 1 | a0018c0028t0001g0133 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.177+3020C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216860 | |||||||
chr17:81216932 | C | T | 1 | a0002c0002t0002g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.177+2948G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216932 | |||||||
chr17:81216935 | ACACCACG others(9): Show |
A | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+2929_177+2944d others(18): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81216935 | |||||||
chr17:81217028 | C | T | 1 | a0004c0005t0001g0281 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.177+2852G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217028 | |||||||
chr17:81217029 | G | A | 1 | a0035c0048t0002g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.177+2851C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217029 | |||||||
chr17:81217060 | A | G | 31 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(28): Show |
35 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.177+2820T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217060 | |||||||
chr17:81217110 | G | A | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.177+2770C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217110 | |||||||
chr17:81217143 | G | C | 1 | a0013c0017t0001g0200 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.177+2737C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217143 | |||||||
chr17:81217248 | A | G | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.177+2632T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217248 | |||||||
chr17:81217293 | G | A | 5 | a0001c0003t0001g0264 a0001c0003t0002g0059 a0001c0003t0002g0060 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+2587C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217293 | |||||||
chr17:81217311 | C | T | 1 | a0002c0002t0002g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.177+2569G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217311 | |||||||
chr17:81217371 | A | G | 17 | a0001c0003t0002g0007 a0001c0003t0002g0049 a0001c0003t0002g0081 others(14): Show |
19 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.177+2509T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217371 | |||||||
chr17:81217410 | C | T | 30 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(27): Show |
34 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.177+2470G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217410 | |||||||
chr17:81217511 | T | G | 6 | a0003c0031t0007g0027 a0011c0015t0006g0319 a0011c0015t0006g0320 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+2369A>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217511 | |||||||
chr17:81217542 | C | T | 5 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0336 others(2): Show |
5 | HG02735.hp2 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.177+2338G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217542 | |||||||
chr17:81217570 | G | A | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.177+2310C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217570 | |||||||
chr17:81217669 | G | A | 1 | a0039c0029t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.177+2211C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217669 | |||||||
chr17:81217912 | A | G | 1 | a0001c0004t0001g0284 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.177+1968T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217912 | |||||||
chr17:81217926 | C | T | 112 | a0001c0003t0001g0264 a0001c0003t0002g0006 a0001c0003t0002g0007 others(109): Show |
128 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.177+1954G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217926 | |||||||
chr17:81217960 | G | C | 1 | a0032c0043t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.177+1920C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217960 | |||||||
chr17:81217984 | A | G | 30 | a0003c0014t0003g0314 a0003c0014t0003g0322 a0003c0014t0003g0324 others(27): Show |
34 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.177+1896T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81217984 | |||||||
chr17:81218001 | TTCTCCC | T | 3 | a0001c0004t0002g0051 a0002c0002t0002g0050 a0002c0002t0002g0052 |
3 | HG02055.hp1 HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.177+1873_177+1878d others(8): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218001 | |||||||
chr17:81218009 | C | T | 1 | a0002c0002t0002g0119 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.177+1871G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218009 | |||||||
chr17:81218027 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18971.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.177+1853G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218027 | |||||||
chr17:81218031 | C | T | 2 | a0001c0003t0002g0006 a0001c0003t0002g0061 |
4 | HG01243.hp1 HG02723.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+1849G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218031 | |||||||
chr17:81218111 | C | T | 1 | a0011c0015t0006g0319 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.177+1769G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218111 | |||||||
chr17:81218114 | C | T | 6 | a0001c0003t0002g0057 a0001c0003t0002g0059 a0001c0003t0002g0060 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+1766G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218114 | |||||||
chr17:81218136 | G | A | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+1744C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218136 | |||||||
chr17:81218148 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0219 |
3 | HG02155.hp1 NA18973.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.177+1732G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218148 | |||||||
chr17:81218152 | C | T | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.177+1728G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218152 | |||||||
chr17:81218193 | C | T | 13 | a0001c0003t0002g0118 a0001c0004t0002g0051 a0001c0004t0002g0053 others(10): Show |
15 | HG00639.hp1 HG02055.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.177+1687G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218193 | |||||||
chr17:81218199 | C | T | 94 | a0001c0003t0002g0006 a0001c0003t0002g0012 a0001c0003t0002g0013 others(91): Show |
105 | HG00323.hp2 HG00639.hp1 HG01070.hp1 others(102): Show |
intron_variant | MODIFIER | c.177+1681G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218199 | |||||||
chr17:81218287 | C | A | 2 | a0001c0001t0001g0201 a0009c0011t0001g0235 |
2 | HG01346.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.177+1593G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218287 | |||||||
chr17:81218319 | G | A | 1 | a0048c0034t0003g0305 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.177+1561C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218319 | |||||||
chr17:81218342 | C | T | 38 | a0001c0003t0002g0037 a0001c0004t0002g0011 a0001c0004t0002g0030 others(35): Show |
46 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.177+1538G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218342 | |||||||
chr17:81218472 | G | C | 1 | a0024c0035t0003g0312 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.177+1408C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218472 | |||||||
chr17:81218504 | A | G | 49 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(46): Show |
57 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.177+1376T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218504 | |||||||
chr17:81218630 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(103): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.177+1250G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218630 | |||||||
chr17:81218631 | G | A | 1 | a0002c0002t0012g0304 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.177+1249C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218631 | |||||||
chr17:81218646 | T | C | 132 | a0001c0003t0002g0006 a0001c0003t0002g0007 a0001c0003t0002g0012 others(129): Show |
152 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.177+1234A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218646 | |||||||
chr17:81218655 | C | T | 1 | a0007c0009t0001g0259 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.177+1225G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218655 | |||||||
chr17:81218972 | A | G | 1 | a0001c0004t0001g0282 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.177+908T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81218972 | |||||||
chr17:81219030 | A | C | 28 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(25): Show |
32 | HG01255.hp2 HG01358.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.177+850T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219030 | |||||||
chr17:81219102 | C | T | 1 | a0027c0053t0002g0032 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.177+778G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219102 | |||||||
chr17:81219124 | A | T | 1 | a0040c0033t0003g0311 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.177+756T>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219124 | |||||||
chr17:81219265 | AC | A | 290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(287): Show |
334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.177+614delG | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219265 | |||||||
chr17:81219292 | C | CT | 18 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(15): Show |
22 | HG01358.hp2 HG02630.hp1 HG02895.hp2 others(19): Show |
intron_variant | MODIFIER | c.177+587dupA | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219292 | |||||||
chr17:81219296 | C | CT | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(250): Show |
293 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.177+583dupA | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219296 | |||||||
chr17:81219296 | C | T | 20 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(17): Show |
24 | HG01358.hp2 HG02630.hp1 HG02895.hp2 others(21): Show |
intron_variant | MODIFIER | c.177+584G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219296 | |||||||
chr17:81219371 | G | A | 20 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(17): Show |
24 | HG01358.hp2 HG02630.hp1 HG02895.hp2 others(21): Show |
intron_variant | MODIFIER | c.177+509C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219371 | |||||||
chr17:81219610 | T | A | 1 | a0001c0018t0001g0214 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.177+270A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219610 | |||||||
chr17:81219650 | CCTGGGGC others(8): Show |
C | 1 | a0001c0004t0001g0282 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.177+215_177+229del others(15): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219650 | |||||||
chr17:81219754 | G | A | 15 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(12): Show |
19 | HG01358.hp2 NA18940.hp1 NA18942.hp2 others(16): Show |
intron_variant | MODIFIER | c.177+126C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219754 | |||||||
chr17:81219792 | C | A | 26 | a0003c0008t0003g0306 a0003c0008t0003g0307 a0003c0008t0003g0308 others(23): Show |
27 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.177+88G>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219792 | |||||||
chr17:81219832 | C | T | 1 | a0037c0041t0001g0242 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.177+48G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219832 | |||||||
chr17:81219857 | G | T | 26 | a0003c0008t0003g0306 a0003c0008t0003g0307 a0003c0008t0003g0308 others(23): Show |
27 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.177+23C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 2/25 | chr17 | 81219857 | |||||||
chr17:81220108 | G | A | 26 | a0003c0008t0003g0306 a0003c0008t0003g0307 a0003c0008t0003g0308 others(23): Show |
27 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-35C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220108 | |||||||
chr17:81220205 | T | C | 108 | a0001c0003t0002g0006 a0001c0003t0002g0007 a0001c0003t0002g0012 others(105): Show |
124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-17-132A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220205 | |||||||
chr17:81220228 | G | A | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-155C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220228 | |||||||
chr17:81220235 | G | A | 2 | a0002c0002t0002g0109 a0002c0002t0002g0110 |
2 | NA18994.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-17-162C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220235 | |||||||
chr17:81220237 | C | T | 1 | a0012c0016t0001g0300 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-17-164G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220237 | |||||||
chr17:81220253 | C | G | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-180G>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220253 | |||||||
chr17:81220292 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-17-219C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220292 | |||||||
chr17:81220320 | G | A | 2 | a0006c0007t0001g0216 a0029c0067t0001g0126 |
2 | HG01928.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-17-247C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220320 | |||||||
chr17:81220339 | G | A | 26 | a0003c0008t0003g0306 a0003c0008t0003g0307 a0003c0008t0003g0308 others(23): Show |
27 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-266C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220339 | |||||||
chr17:81220390 | G | A | 1 | a0038c0055t0009g0092 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-17-317C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220390 | |||||||
chr17:81220449 | G | A | 1 | a0005c0006t0001g0255 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-17-376C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220449 | |||||||
chr17:81220516 | CAG | C | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-445_-17-444del others(2): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220516 | |||||||
chr17:81220530 | T | C | 26 | a0003c0008t0003g0306 a0003c0008t0003g0307 a0003c0008t0003g0308 others(23): Show |
27 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-457A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220530 | |||||||
chr17:81220546 | G | A | 1 | a0047c0069t0002g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-473C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220546 | |||||||
chr17:81220587 | C | T | 5 | a0007c0009t0001g0259 a0007c0009t0001g0260 a0007c0009t0001g0261 others(2): Show |
5 | HG02886.hp1 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-514G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220587 | |||||||
chr17:81220597 | C | T | 108 | a0001c0003t0002g0006 a0001c0003t0002g0007 a0001c0003t0002g0012 others(105): Show |
124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-17-524G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220597 | |||||||
chr17:81220638 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-17-565C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220638 | |||||||
chr17:81220643 | C | T | 20 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(17): Show |
24 | HG01358.hp2 HG02630.hp1 HG02895.hp2 others(21): Show |
intron_variant | MODIFIER | c.-17-570G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220643 | |||||||
chr17:81220691 | G | C | 7 | a0015c0022t0001g0129 a0015c0022t0001g0130 a0015c0022t0001g0131 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-618C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220691 | |||||||
chr17:81220692 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-17-619C>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220692 | |||||||
chr17:81220762 | A | C | 1 | a0001c0004t0001g0298 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-17-689T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220762 | |||||||
chr17:81220796 | C | T | 6 | a0010c0013t0004g0333 a0010c0013t0004g0334 a0010c0013t0004g0335 others(3): Show |
6 | HG02735.hp2 HG03239.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-723G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220796 | |||||||
chr17:81220805 | A | G | 1 | a0002c0002t0002g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-732T>C | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220805 | |||||||
chr17:81220981 | C | T | 108 | a0001c0003t0002g0006 a0001c0003t0002g0007 a0001c0003t0002g0012 others(105): Show |
124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-17-908G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220981 | |||||||
chr17:81220993 | C | T | 1 | a0031c0070t0001g0127 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-17-920G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220993 | |||||||
chr17:81220994 | G | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(118): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-17-921C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81220994 | |||||||
chr17:81221077 | A | C | 2 | a0001c0001t0001g0218 a0035c0048t0002g0031 |
2 | HG02027.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-17-1004T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221077 | |||||||
chr17:81221124 | C | CA | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(126): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-17-1052dupT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221124 | |||||||
chr17:81221124 | C | CAA | 34 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0218 others(31): Show |
37 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.-17-1053_-17-1052d others(4): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221124 | |||||||
chr17:81221124 | CA | C | 36 | a0001c0004t0002g0030 a0003c0008t0003g0306 a0003c0008t0003g0307 others(33): Show |
40 | HG01257.hp2 HG01358.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-17-1052delT | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221124 | |||||||
chr17:81221132 | A | C | 1 | a0026c0072t0001g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-17-1059T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221132 | |||||||
chr17:81221137 | A | C | 1 | a0048c0034t0003g0305 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-17-1064T>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221137 | |||||||
chr17:81221221 | C | T | 109 | a0001c0003t0002g0006 a0001c0003t0002g0007 a0001c0003t0002g0012 others(106): Show |
125 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-17-1148G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221221 | |||||||
chr17:81221406 | G | A | 26 | a0003c0008t0003g0306 a0003c0008t0003g0307 a0003c0008t0003g0308 others(23): Show |
27 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-1333C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221406 | |||||||
chr17:81221489 | G | C | 1 | a0003c0008t0003g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-18+1280C>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221489 | |||||||
chr17:81221569 | TCTC | T | 20 | a0005c0006t0001g0005 a0005c0006t0001g0022 a0005c0006t0001g0248 others(17): Show |
24 | HG01358.hp2 HG02630.hp1 HG02895.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18+1197_-18+1199d others(5): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221569 | |||||||
chr17:81221596 | C | T | 1 | a0003c0031t0007g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-18+1173G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221596 | |||||||
chr17:81221624 | G | A | 1 | a0001c0003t0002g0118 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-18+1145C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221624 | |||||||
chr17:81221824 | C | T | 2 | a0001c0003t0002g0028 a0001c0003t0002g0029 |
2 | HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+945G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81221824 | |||||||
chr17:81222014 | T | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(118): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-18+755A>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81222014 | |||||||
chr17:81222083 | G | A | 1 | a0002c0002t0002g0119 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-18+686C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81222083 | |||||||
chr17:81222296 | G | GCTGACC | 4 | a0002c0002t0002g0014 a0002c0002t0002g0015 a0002c0002t0002g0120 others(1): Show |
6 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+467_-18+472dup others(6): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81222296 | |||||||
chr17:81222296 | GCTGACC | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(158): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.-18+467_-18+472del others(6): Show |
CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81222296 | |||||||
chr17:81222322 | T | C | 1 | a0039c0029t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18+447A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81222322 | |||||||
chr17:81222447 | T | C | 1 | a0001c0004t0001g0302 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-18+322A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81222447 | |||||||
chr17:81222543 | C | T | 26 | a0003c0008t0003g0306 a0003c0008t0003g0307 a0003c0008t0003g0308 others(23): Show |
27 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+226G>A | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81222543 | |||||||
chr17:81222595 | T | C | 1 | a0026c0072t0001g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-18+174A>G | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81222595 | |||||||
chr17:81222648 | G | A | 29 | a0001c0058t0003g0331 a0003c0008t0003g0306 a0003c0008t0003g0307 others(26): Show |
30 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.-18+121C>T | CEP131 | ENSG00000141577.14 | transcript | ENST00000450824.7 | protein_coding | 1/25 | chr17 | 81222648 |