Item | Value |
---|---|
geneid | 11215 |
ensemblid | ENSG00000023516.9 |
hgncid | 369 |
symbol | AKAP11 |
name | A-kinase anchoring protein 11 |
refseq_nuc | NM_016248.4 |
refseq_prot | NP_057332.1 |
ensembl_nuc | ENST00000025301.4 |
ensembl_prot | ENSP00000025301.2 |
mane_status | MANE Select |
chr | chr13 |
start | 42272152 |
end | 42323261 |
strand | + |
ver | v1.2 |
region | chr13:42272152-42323261 |
region5000 | chr13:42267152-42328261 |
regionname0 | AKAP11_chr13_42272152_42323261 |
regionname5000 | AKAP11_chr13_42267152_42328261 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1901 | 319 | 75 | 66 | 129 | 16 | 31 | 103 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0002 | 0/0 | 1901 | 17 | 1 | 0 | 15 | 0 | 1 | 12 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0003 | 0/0 | 1901 | 11 | 0 | 0 | 10 | 0 | 1 | 6 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0004 | 0/0 | 1901 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0005 | 0/0 | 1901 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0006 | 0/0 | 1901 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0007 | 0/0 | 1901 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0008 | 0/0 | 1901 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0009 | 0/0 | 1901 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0010 | 0/0 | 1901 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0011 | 0/0 | 1901 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0012 | 0/0 | 1901 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0013 | 0/0 | 1901 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0014 | 0/0 | 1901 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0015 | 0/0 | 1901 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0016 | 0/0 | 1901 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0017 | 0/0 | 1901 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0018 | 0/0 | 1901 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0019 | 0/0 | 1901 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0020 | 0/0 | 1901 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0021 | 0/0 | 1901 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0022 | 0/0 | 1901 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
a0023 | 0/0 | 1901 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | MATFR others(1896): Show |
chr13 | 42267152 | 42328261 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 5703 | 245 | 56 | 54 | 100 | 9 | 24 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0001c0002 | 0/0 | 5703 | 38 | 1 | 5 | 26 | 3 | 3 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0001c0003 | 0/0 | 5703 | 27 | 17 | 4 | 0 | 4 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0001c0006 | 0/0 | 5703 | 4 | 0 | 2 | 0 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0001c0010 | 0/0 | 5703 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0001c0019 | 0/0 | 5703 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0001c0026 | 0/0 | 5703 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0002c0004 | 0/0 | 5703 | 17 | 1 | 0 | 15 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0003c0005 | 0/0 | 5703 | 10 | 0 | 0 | 9 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0003c0022 | 0/0 | 5703 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0004c0009 | 0/0 | 5703 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0005c0007 | 0/0 | 5703 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0006c0008 | 0/0 | 5703 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0007c0013 | 0/0 | 5703 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0008c0011 | 0/0 | 5703 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0009c0014 | 0/0 | 5703 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0010c0015 | 0/0 | 5703 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0011c0012 | 0/0 | 5703 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0012c0021 | 0/0 | 5703 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0013c0023 | 0/0 | 5703 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0014c0030 | 0/0 | 5703 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0015c0020 | 0/0 | 5703 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0016c0018 | 0/0 | 5703 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0017c0017 | 0/0 | 5703 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0018c0027 | 0/0 | 5703 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0019c0028 | 0/0 | 5703 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0020c0025 | 0/0 | 5703 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0021c0016 | 0/0 | 5703 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0022c0024 | 0/0 | 5703 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 | ||
a0023c0029 | 0/0 | 5703 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | ATGGC others(5698): Show |
chr13 | 42267152 | 42328261 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 9917 | 22 | 8 | 0 | 10 | 0 | 4 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0003 | 0/0 | 9923 | 14 | 0 | 7 | 5 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9918): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0004 | 0/0 | 9921 | 13 | 1 | 1 | 11 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9916): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0005 | 0/0 | 9929 | 13 | 0 | 4 | 8 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9924): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0006 | 0/0 | 9921 | 13 | 0 | 6 | 5 | 2 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9916): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0007 | 1/0 | 9915 | 9 | 0 | 0 | 8 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9910): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0009 | 0/0 | 9919 | 11 | 0 | 2 | 6 | 0 | 3 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0011 | 0/0 | 9911 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0012 | 0/1 | 9913 | 8 | 0 | 4 | 0 | 2 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0013 | 0/0 | 9917 | 8 | 7 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0014 | 0/0 | 9925 | 9 | 0 | 4 | 4 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9920): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0015 | 0/0 | 9917 | 9 | 8 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0016 | 0/0 | 9927 | 8 | 0 | 5 | 0 | 3 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9922): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0018 | 0/0 | 9913 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0019 | 0/0 | 9925 | 8 | 5 | 0 | 2 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9920): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0020 | 0/0 | 9927 | 8 | 2 | 2 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9922): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0021 | 0/0 | 9921 | 7 | 0 | 0 | 7 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9916): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0023 | 0/0 | 9919 | 6 | 1 | 0 | 4 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0024 | 0/0 | 9931 | 6 | 0 | 1 | 3 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9926): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0026 | 0/0 | 9925 | 5 | 0 | 3 | 0 | 2 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9920): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0027 | 0/0 | 9923 | 3 | 0 | 3 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9918): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0028 | 0/0 | 9919 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0029 | 0/0 | 9917 | 4 | 0 | 0 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0030 | 0/0 | 9919 | 4 | 0 | 0 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0031 | 0/0 | 9913 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0032 | 0/0 | 9923 | 3 | 1 | 1 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9918): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0033 | 0/0 | 9933 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9928): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0035 | 0/0 | 9929 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9924): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0036 | 0/0 | 9891 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9886): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0037 | 0/0 | 9923 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9918): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0043 | 0/0 | 9917 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0044 | 0/0 | 9917 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0045 | 0/0 | 9917 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0046 | 0/0 | 9917 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0047 | 0/0 | 9921 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9916): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0048 | 0/0 | 9923 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9918): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0050 | 0/0 | 9927 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9922): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0051 | 0/0 | 9901 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9896): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0052 | 0/0 | 9913 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0053 | 0/0 | 9913 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0054 | 0/0 | 9909 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9904): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0055 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0056 | 0/0 | 9911 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0057 | 0/0 | 9921 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9916): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0058 | 0/0 | 9923 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9918): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0059 | 0/0 | 9923 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9918): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0060 | 0/0 | 9915 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9910): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0061 | 0/0 | 9917 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0062 | 0/0 | 9927 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9922): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0063 | 0/0 | 9933 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9928): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0064 | 0/0 | 9925 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9920): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0066 | 0/0 | 9927 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9922): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0067 | 0/0 | 9937 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9932): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0068 | 0/0 | 9929 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9924): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0069 | 0/0 | 9939 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9934): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0070 | 0/0 | 9931 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9926): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0071 | 0/0 | 9929 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9924): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0074 | 0/0 | 9899 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9894): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0079 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0082 | 0/0 | 9921 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9916): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0084 | 0/0 | 9927 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9922): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0085 | 0/0 | 9929 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9924): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0086 | 0/0 | 9931 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9926): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0090 | 0/0 | 9927 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9922): Show |
chr13 | 42267152 | 42328261 |
a0001c0001t0092 | 0/0 | 9923 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9918): Show |
chr13 | 42267152 | 42328261 |
a0001c0002t0001 | 0/0 | 9911 | 27 | 0 | 4 | 18 | 3 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0001c0002t0017 | 0/0 | 9913 | 9 | 0 | 1 | 8 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0001c0002t0087 | 0/0 | 9911 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0001c0002t0088 | 0/0 | 9913 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0001c0003t0010 | 0/0 | 9917 | 10 | 2 | 4 | 0 | 3 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0001c0003t0022 | 0/0 | 9915 | 5 | 5 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9910): Show |
chr13 | 42267152 | 42328261 |
a0001c0003t0025 | 0/0 | 9911 | 6 | 6 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0001c0003t0038 | 0/0 | 9913 | 2 | 0 | 0 | 0 | 1 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0001c0003t0077 | 0/0 | 9915 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9910): Show |
chr13 | 42267152 | 42328261 |
a0001c0003t0089 | 0/0 | 9915 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9910): Show |
chr13 | 42267152 | 42328261 |
a0001c0003t0093 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0001c0003t0094 | 0/0 | 9921 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9916): Show |
chr13 | 42267152 | 42328261 |
a0001c0006t0001 | 0/0 | 9911 | 4 | 0 | 2 | 0 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0001c0010t0016 | 0/0 | 9927 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9922): Show |
chr13 | 42267152 | 42328261 |
a0001c0010t0027 | 0/0 | 9923 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9918): Show |
chr13 | 42267152 | 42328261 |
a0001c0019t0081 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0001c0026t0001 | 0/0 | 9911 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0002c0004t0007 | 0/0 | 9915 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9910): Show |
chr13 | 42267152 | 42328261 |
a0002c0004t0011 | 0/0 | 9911 | 6 | 0 | 0 | 6 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0002c0004t0018 | 0/0 | 9913 | 7 | 1 | 0 | 6 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0002c0004t0042 | 0/0 | 9913 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0003c0005t0008 | 0/0 | 9913 | 9 | 0 | 0 | 9 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0003c0005t0075 | 0/0 | 9909 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9904): Show |
chr13 | 42267152 | 42328261 |
a0003c0022t0008 | 0/0 | 9913 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0004c0009t0072 | 0/0 | 9917 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0004c0009t0073 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0004c0009t0080 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0005c0007t0034 | 0/0 | 9921 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9916): Show |
chr13 | 42267152 | 42328261 |
a0005c0007t0039 | 0/0 | 9919 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0006c0008t0040 | 0/0 | 9915 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9910): Show |
chr13 | 42267152 | 42328261 |
a0006c0008t0091 | 0/0 | 9917 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0007c0013t0008 | 0/0 | 9913 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0008c0011t0011 | 0/0 | 9911 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0009c0014t0022 | 0/0 | 9915 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9910): Show |
chr13 | 42267152 | 42328261 |
a0010c0015t0013 | 0/0 | 9917 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9912): Show |
chr13 | 42267152 | 42328261 |
a0010c0015t0028 | 0/0 | 9919 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9914): Show |
chr13 | 42267152 | 42328261 |
a0011c0012t0034 | 0/0 | 9921 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9916): Show |
chr13 | 42267152 | 42328261 |
a0012c0021t0012 | 0/0 | 9913 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9908): Show |
chr13 | 42267152 | 42328261 |
a0013c0023t0078 | 0/0 | 9915 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9910): Show |
chr13 | 42267152 | 42328261 |
a0014c0030t0083 | 0/0 | 9927 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9922): Show |
chr13 | 42267152 | 42328261 |
a0015c0020t0095 | 0/0 | 9923 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9918): Show |
chr13 | 42267152 | 42328261 |
a0016c0018t0076 | 0/0 | 9911 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0017c0017t0041 | 0/0 | 9907 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9902): Show |
chr13 | 42267152 | 42328261 |
a0018c0027t0001 | 0/0 | 9911 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0019c0028t0001 | 0/0 | 9911 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0020c0025t0001 | 0/0 | 9911 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9906): Show |
chr13 | 42267152 | 42328261 |
a0021c0016t0065 | 0/0 | 9927 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9922): Show |
chr13 | 42267152 | 42328261 |
a0022c0024t0049 | 0/0 | 9925 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9920): Show |
chr13 | 42267152 | 42328261 |
a0023c0029t0026 | 0/0 | 9925 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | AGCTT others(9920): Show |
chr13 | 42267152 | 42328261 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0003 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0004g0004 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0004g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0005g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0006g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0006g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0006g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0007g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0007g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0009g0002 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0009g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0009g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0009g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0009g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0009g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0009g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0011g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0012g0007 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0012g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0012g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0013g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0013g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0013g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0013g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0013g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0013g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0013g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0014g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0014g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0014g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0014g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0014g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0014g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0015g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0015g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0015g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0015g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0015g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0016g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0016g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0016g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0016g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0016g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0016g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0016g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0016g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0018g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0019g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0019g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0019g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0019g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0019g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0019g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0019g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0020g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0020g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0020g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0020g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0020g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0020g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0020g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0021g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0021g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0021g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0021g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0021g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0023g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0023g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0023g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0023g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0024g0002 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0024g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0026g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0026g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0026g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0026g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0027g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0028g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0028g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0028g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0029g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0029g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0029g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0030g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0031g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0032g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0032g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0033g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0033g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0033g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0035g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0035g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0035g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0036g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0036g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0037g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0037g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0043g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0044g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0045g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0046g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0047g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0048g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0050g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0051g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0052g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0053g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0054g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0055g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0056g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0057g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0058g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0059g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0060g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0061g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0062g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0063g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0064g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0066g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0067g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0068g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0069g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0070g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0071g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0074g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0079g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0082g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0084g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0085g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0086g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0090g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0001t0092g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0001g0001 | 0/0 | 15 | 0 | 3 | 11 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0017g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0017g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0017g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0017g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0017g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0087g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0002t0088g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0010g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0010g0023 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0010g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0010g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0010g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0010g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0022g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0022g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0022g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0022g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0022g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0025g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0025g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0025g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0025g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0038g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0077g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0089g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0093g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0003t0094g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0006t0001g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0006t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0010t0016g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0010t0027g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0019t0081g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0001c0026t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0002c0004t0007g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0002c0004t0007g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0002c0004t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0002c0004t0011g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0002c0004t0011g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0002c0004t0011g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0002c0004t0011g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0002c0004t0018g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0002c0004t0018g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0002c0004t0018g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0002c0004t0042g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0003c0005t0008g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0003c0005t0075g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0003c0022t0008g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0004c0009t0072g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0004c0009t0073g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0004c0009t0080g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0005c0007t0034g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0005c0007t0039g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0005c0007t0039g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0006c0008t0040g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0006c0008t0091g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0007c0013t0008g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0008c0011t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0008c0011t0011g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0009c0014t0022g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0009c0014t0022g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0010c0015t0013g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0010c0015t0028g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0011c0012t0034g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0012c0021t0012g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0013c0023t0078g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0014c0030t0083g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0015c0020t0095g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0016c0018t0076g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0017c0017t0041g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0018c0027t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0019c0028t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0020c0025t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0021c0016t0065g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0022c0024t0049g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
a0023c0029t0026g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0038 | g0017 | EUR | GBR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00099 | hp2 | a0001 | c0001 | t0016 | g0162 | EUR | GBR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00140 | hp1 | a0001 | c0001 | t0012 | g0007 | EUR | GBR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0101 | EUR | GBR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00323 | hp1 | a0001 | c0003 | t0010 | g0023 | EUR | FIN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00323 | hp2 | a0001 | c0001 | t0016 | g0158 | EUR | FIN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00408 | hp1 | a0002 | c0004 | t0007 | g0124 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00408 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00423 | hp1 | a0002 | c0004 | t0011 | g0011 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00423 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00438 | hp2 | a0001 | c0001 | t0029 | g0005 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00544 | hp1 | a0001 | c0001 | t0020 | g0176 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00544 | hp2 | a0001 | c0001 | t0020 | g0075 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00597 | hp2 | a0001 | c0001 | t0033 | g0093 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00609 | hp1 | a0001 | c0001 | t0029 | g0078 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00609 | hp2 | a0007 | c0013 | t0008 | g0006 | EAS | CHS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00639 | hp2 | a0001 | c0003 | t0010 | g0017 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00642 | hp1 | a0001 | c0006 | t0001 | g0001 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00733 | hp2 | a0001 | c0001 | t0012 | g0007 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00735 | hp2 | a0001 | c0001 | t0035 | g0012 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00738 | hp1 | a0001 | c0006 | t0001 | g0001 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00738 | hp2 | a0001 | c0001 | t0009 | g0079 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0071 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG00741 | hp2 | a0001 | c0001 | t0020 | g0004 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01070 | hp2 | a0001 | c0001 | t0014 | g0032 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01071 | hp1 | a0001 | c0002 | t0017 | g0001 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01071 | hp2 | a0001 | c0001 | t0014 | g0032 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0073 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0085 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01081 | hp1 | a0001 | c0001 | t0016 | g0163 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01099 | hp1 | a0001 | c0001 | t0016 | g0160 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0103 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01106 | hp2 | a0001 | c0001 | t0016 | g0025 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01109 | hp1 | a0008 | c0011 | t0011 | g0121 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0074 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01167 | hp1 | a0001 | c0001 | t0084 | g0012 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01167 | hp2 | a0001 | c0001 | t0014 | g0080 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01243 | hp1 | a0001 | c0001 | t0012 | g0007 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01243 | hp2 | a0001 | c0001 | t0052 | g0049 | AMR | PUR | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01256 | hp1 | a0010 | c0015 | t0013 | g0181 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01256 | hp2 | a0001 | c0003 | t0010 | g0042 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01257 | hp1 | a0001 | c0001 | t0032 | g0004 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01257 | hp2 | a0001 | c0001 | t0027 | g0012 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01258 | hp1 | a0001 | c0001 | t0027 | g0012 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01258 | hp2 | a0001 | c0003 | t0010 | g0042 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01261 | hp1 | a0001 | c0001 | t0061 | g0070 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01261 | hp2 | a0012 | c0021 | t0012 | g0007 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01346 | hp1 | a0001 | c0001 | t0014 | g0013 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01346 | hp2 | a0001 | c0001 | t0012 | g0007 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01358 | hp1 | a0001 | c0001 | t0012 | g0007 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0009 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01361 | hp1 | a0001 | c0003 | t0010 | g0146 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01361 | hp2 | a0001 | c0001 | t0020 | g0092 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01496 | hp1 | a0001 | c0001 | t0016 | g0166 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01496 | hp2 | a0001 | c0001 | t0053 | g0049 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0026 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01515 | hp2 | a0001 | c0001 | t0026 | g0159 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01516 | hp1 | a0001 | c0001 | t0026 | g0168 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01516 | hp2 | a0001 | c0003 | t0010 | g0023 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0052 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01517 | hp2 | a0001 | c0003 | t0010 | g0143 | EUR | IBS | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01884 | hp1 | a0001 | c0003 | t0022 | g0149 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01884 | hp2 | a0001 | c0001 | t0020 | g0072 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01891 | hp1 | a0001 | c0001 | t0085 | g0138 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01891 | hp2 | a0004 | c0009 | t0072 | g0173 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01928 | hp1 | a0001 | c0001 | t0006 | g0013 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01928 | hp2 | a0001 | c0001 | t0092 | g0010 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01943 | hp1 | a0001 | c0001 | t0033 | g0002 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01943 | hp2 | a0001 | c0001 | t0026 | g0025 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01952 | hp1 | a0001 | c0001 | t0086 | g0044 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01975 | hp1 | a0001 | c0001 | t0026 | g0107 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01975 | hp2 | a0001 | c0001 | t0015 | g0109 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01978 | hp2 | a0001 | c0001 | t0016 | g0044 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01981 | hp1 | a0001 | c0001 | t0009 | g0013 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01981 | hp2 | a0011 | c0012 | t0034 | g0035 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01993 | hp2 | a0001 | c0001 | t0026 | g0025 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02004 | hp1 | a0001 | c0001 | t0047 | g0130 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02004 | hp2 | a0001 | c0001 | t0006 | g0013 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02015 | hp1 | a0002 | c0004 | t0011 | g0136 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02015 | hp2 | a0001 | c0001 | t0044 | g0003 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02074 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02083 | hp2 | a0001 | c0001 | t0090 | g0167 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02132 | hp1 | a0001 | c0001 | t0009 | g0002 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02132 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02135 | hp1 | a0001 | c0001 | t0014 | g0095 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02145 | hp1 | a0001 | c0001 | t0013 | g0178 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02145 | hp2 | a0004 | c0009 | t0080 | g0174 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02148 | hp1 | a0001 | c0001 | t0060 | g0097 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02148 | hp2 | a0001 | c0010 | t0016 | g0045 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | CDX | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02155 | hp2 | a0001 | c0001 | t0024 | g0002 | EAS | CDX | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02165 | hp1 | a0003 | c0022 | t0008 | g0199 | EAS | CDX | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02165 | hp2 | a0001 | c0001 | t0030 | g0005 | EAS | CDX | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02257 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02257 | hp2 | a0001 | c0003 | t0010 | g0043 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02258 | hp1 | a0001 | c0001 | t0013 | g0185 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02258 | hp2 | a0001 | c0003 | t0010 | g0043 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02293 | hp1 | a0009 | c0014 | t0022 | g0151 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02293 | hp2 | a0001 | c0001 | t0024 | g0002 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02300 | hp2 | a0001 | c0001 | t0027 | g0012 | AMR | PEL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02451 | hp1 | a0001 | c0003 | t0022 | g0148 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02451 | hp2 | a0002 | c0004 | t0018 | g0126 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02523 | hp1 | a0001 | c0001 | t0068 | g0002 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02523 | hp2 | a0001 | c0001 | t0035 | g0165 | EAS | KHV | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02572 | hp1 | a0001 | c0003 | t0025 | g0145 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02602 | hp1 | a0001 | c0003 | t0038 | g0017 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0029 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02615 | hp1 | a0001 | c0001 | t0031 | g0016 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02615 | hp2 | a0001 | c0001 | t0013 | g0184 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02622 | hp1 | a0001 | c0003 | t0089 | g0017 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02622 | hp2 | a0001 | c0001 | t0019 | g0186 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02630 | hp1 | a0001 | c0001 | t0015 | g0112 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02630 | hp2 | a0001 | c0001 | t0028 | g0187 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02647 | hp2 | a0011 | c0012 | t0034 | g0035 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02698 | hp1 | a0001 | c0006 | t0001 | g0053 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02698 | hp2 | a0001 | c0001 | t0071 | g0062 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02717 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02717 | hp2 | a0001 | c0003 | t0022 | g0150 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02723 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02735 | hp1 | a0013 | c0023 | t0078 | g0200 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02735 | hp2 | a0001 | c0001 | t0012 | g0119 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02738 | hp2 | a0001 | c0001 | t0019 | g0029 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02809 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02809 | hp2 | a0001 | c0001 | t0055 | g0190 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02818 | hp1 | a0001 | c0003 | t0025 | g0024 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02886 | hp2 | a0001 | c0003 | t0025 | g0024 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02895 | hp1 | a0001 | c0003 | t0022 | g0144 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02895 | hp2 | a0001 | c0001 | t0057 | g0191 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02896 | hp1 | a0001 | c0001 | t0031 | g0016 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02896 | hp2 | a0001 | c0001 | t0015 | g0110 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02897 | hp1 | a0001 | c0003 | t0022 | g0147 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02897 | hp2 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02922 | hp1 | a0004 | c0009 | t0073 | g0175 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02922 | hp2 | a0014 | c0030 | t0083 | g0194 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02965 | hp1 | a0008 | c0011 | t0011 | g0117 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02965 | hp2 | a0001 | c0003 | t0025 | g0024 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0198 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02976 | hp2 | a0001 | c0001 | t0036 | g0129 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03017 | hp1 | a0001 | c0001 | t0009 | g0068 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03017 | hp2 | a0001 | c0001 | t0013 | g0048 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03041 | hp1 | a0001 | c0001 | t0011 | g0170 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03098 | hp1 | a0001 | c0001 | t0019 | g0033 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03098 | hp2 | a0005 | c0007 | t0034 | g0142 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03139 | hp1 | a0001 | c0003 | t0093 | g0157 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03139 | hp2 | a0001 | c0001 | t0013 | g0182 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03195 | hp1 | a0001 | c0001 | t0036 | g0040 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03195 | hp2 | a0001 | c0001 | t0074 | g0139 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03225 | hp1 | a0001 | c0001 | t0031 | g0016 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03225 | hp2 | a0001 | c0001 | t0028 | g0188 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03239 | hp1 | a0001 | c0001 | t0024 | g0002 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03239 | hp2 | a0001 | c0001 | t0024 | g0102 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03453 | hp1 | a0001 | c0001 | t0028 | g0104 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03486 | hp1 | a0001 | c0001 | t0019 | g0033 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03486 | hp2 | a0001 | c0001 | t0020 | g0021 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03491 | hp1 | a0001 | c0001 | t0056 | g0031 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03491 | hp2 | a0001 | c0001 | t0048 | g0003 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03516 | hp1 | a0015 | c0020 | t0095 | g0154 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03516 | hp2 | a0001 | c0001 | t0019 | g0064 | AFR | ESN | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03540 | hp1 | a0001 | c0001 | t0015 | g0111 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03540 | hp2 | a0001 | c0019 | t0081 | g0172 | AFR | GWD | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03579 | hp1 | a0001 | c0001 | t0058 | g0189 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03579 | hp2 | a0005 | c0007 | t0039 | g0141 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03654 | hp1 | a0001 | c0001 | t0009 | g0002 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03654 | hp2 | a0001 | c0001 | t0063 | g0094 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03688 | hp2 | a0001 | c0001 | t0009 | g0002 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03710 | hp1 | a0001 | c0002 | t0087 | g0001 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03831 | hp1 | a0016 | c0018 | t0076 | g0106 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03834 | hp1 | a0001 | c0003 | t0010 | g0023 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03942 | hp1 | a0001 | c0006 | t0001 | g0001 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03942 | hp2 | a0001 | c0001 | t0050 | g0003 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG04184 | hp1 | a0001 | c0001 | t0082 | g0012 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG04184 | hp2 | a0001 | c0001 | t0014 | g0002 | SAS | BEB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG04199 | hp1 | a0001 | c0001 | t0023 | g0133 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG04199 | hp2 | a0002 | c0004 | t0042 | g0125 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG04204 | hp1 | a0003 | c0005 | t0075 | g0063 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG04204 | hp2 | a0017 | c0017 | t0041 | g0197 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG04228 | hp1 | a0001 | c0001 | t0043 | g0114 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | STU | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18522 | hp1 | a0001 | c0002 | t0088 | g0051 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18522 | hp2 | a0001 | c0001 | t0067 | g0021 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18612 | hp1 | a0001 | c0001 | t0023 | g0003 | EAS | CHB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18612 | hp2 | a0001 | c0001 | t0051 | g0002 | EAS | CHB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18906 | hp1 | a0001 | c0001 | t0046 | g0015 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18906 | hp2 | a0001 | c0001 | t0013 | g0067 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18939 | hp1 | a0001 | c0001 | t0014 | g0019 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18939 | hp2 | a0002 | c0004 | t0018 | g0137 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18940 | hp1 | a0018 | c0027 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18940 | hp2 | a0001 | c0001 | t0064 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18941 | hp1 | a0019 | c0028 | t0001 | g0059 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18944 | hp1 | a0001 | c0001 | t0021 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18944 | hp2 | a0020 | c0025 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18945 | hp2 | a0006 | c0008 | t0040 | g0022 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18946 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18946 | hp2 | a0001 | c0001 | t0029 | g0030 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18947 | hp2 | a0001 | c0001 | t0023 | g0134 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18948 | hp1 | a0006 | c0008 | t0091 | g0022 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18950 | hp1 | a0001 | c0001 | t0021 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18950 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18951 | hp1 | a0021 | c0016 | t0065 | g0034 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18957 | hp1 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18957 | hp2 | a0001 | c0002 | t0017 | g0018 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18959 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18959 | hp2 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18961 | hp1 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18961 | hp2 | a0001 | c0001 | t0014 | g0020 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18962 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18962 | hp2 | a0001 | c0026 | t0001 | g0027 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18966 | hp1 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18966 | hp2 | a0001 | c0001 | t0020 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18967 | hp1 | a0001 | c0001 | t0037 | g0096 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18967 | hp2 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18969 | hp2 | a0001 | c0010 | t0027 | g0046 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18972 | hp1 | a0002 | c0004 | t0018 | g0011 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18972 | hp2 | a0001 | c0002 | t0017 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18978 | hp2 | a0001 | c0001 | t0023 | g0003 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18979 | hp1 | a0002 | c0004 | t0011 | g0041 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18979 | hp2 | a0001 | c0001 | t0021 | g0099 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18980 | hp1 | a0001 | c0001 | t0030 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18982 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18982 | hp2 | a0001 | c0001 | t0054 | g0009 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18983 | hp1 | a0001 | c0001 | t0019 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18983 | hp2 | a0001 | c0001 | t0019 | g0091 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18984 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18984 | hp2 | a0001 | c0001 | t0009 | g0087 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18985 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18985 | hp2 | a0002 | c0004 | t0018 | g0011 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18986 | hp1 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18986 | hp2 | a0002 | c0004 | t0018 | g0011 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18992 | hp1 | a0001 | c0001 | t0007 | g0122 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18992 | hp2 | a0001 | c0001 | t0024 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18993 | hp1 | a0001 | c0001 | t0023 | g0003 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18993 | hp2 | a0001 | c0001 | t0009 | g0065 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18994 | hp1 | a0002 | c0004 | t0011 | g0038 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18994 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18999 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19000 | hp1 | a0001 | c0001 | t0035 | g0164 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19000 | hp2 | a0001 | c0001 | t0033 | g0098 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19001 | hp1 | a0001 | c0002 | t0017 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19001 | hp2 | a0001 | c0001 | t0021 | g0088 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19003 | hp2 | a0001 | c0001 | t0021 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19005 | hp1 | a0001 | c0001 | t0037 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19007 | hp1 | a0002 | c0004 | t0018 | g0011 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19010 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19010 | hp2 | a0001 | c0001 | t0029 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19012 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19012 | hp2 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19030 | hp1 | a0001 | c0001 | t0069 | g0021 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19030 | hp2 | a0022 | c0024 | t0049 | g0131 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19043 | hp1 | a0001 | c0001 | t0059 | g0048 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19043 | hp2 | a0001 | c0001 | t0013 | g0180 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19054 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19054 | hp2 | a0001 | c0001 | t0014 | g0105 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19055 | hp1 | a0001 | c0001 | t0070 | g0020 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19056 | hp1 | a0006 | c0008 | t0040 | g0022 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19056 | hp2 | a0002 | c0004 | t0018 | g0011 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19058 | hp1 | a0001 | c0002 | t0017 | g0018 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19058 | hp2 | a0001 | c0001 | t0021 | g0030 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19062 | hp1 | a0001 | c0010 | t0027 | g0046 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19062 | hp2 | a0001 | c0001 | t0021 | g0089 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19064 | hp1 | a0002 | c0004 | t0011 | g0038 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19065 | hp1 | a0001 | c0002 | t0017 | g0018 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19065 | hp2 | a0001 | c0001 | t0020 | g0084 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19067 | hp1 | a0001 | c0002 | t0017 | g0050 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19067 | hp2 | a0001 | c0001 | t0066 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19070 | hp2 | a0023 | c0029 | t0026 | g0045 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19077 | hp1 | a0003 | c0005 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19079 | hp1 | a0002 | c0004 | t0007 | g0127 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19080 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19081 | hp2 | a0001 | c0001 | t0030 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19082 | hp1 | a0002 | c0004 | t0007 | g0123 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19084 | hp1 | a0001 | c0002 | t0017 | g0054 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19084 | hp2 | a0001 | c0001 | t0024 | g0002 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19085 | hp1 | a0007 | c0013 | t0008 | g0006 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19086 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19086 | hp2 | a0001 | c0002 | t0017 | g0060 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19087 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19091 | hp1 | a0002 | c0004 | t0011 | g0041 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA19240 | hp2 | a0005 | c0007 | t0039 | g0140 | AFR | YRI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA20129 | hp1 | a0001 | c0001 | t0062 | g0100 | AFR | ASW | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA20129 | hp2 | a0001 | c0003 | t0025 | g0156 | AFR | ASW | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA20752 | hp1 | a0001 | c0001 | t0006 | g0069 | EUR | TSI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA20752 | hp2 | a0001 | c0001 | t0016 | g0161 | EUR | TSI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA20805 | hp1 | a0001 | c0001 | t0012 | g0007 | EUR | TSI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01123 | hp1 | a0009 | c0014 | t0022 | g0152 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0077 | AMR | CLM | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02109 | hp1 | a0001 | c0003 | t0025 | g0155 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02109 | hp2 | a0001 | c0001 | t0031 | g0016 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02559 | hp1 | a0001 | c0001 | t0023 | g0116 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG02559 | hp2 | a0001 | c0001 | t0013 | g0183 | AFR | ACB | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03471 | hp1 | a0010 | c0015 | t0028 | g0179 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG03471 | hp2 | a0001 | c0001 | t0079 | g0108 | AFR | MSL | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG06807 | hp1 | a0001 | c0003 | t0094 | g0153 | AFR | USA | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
HG06807 | hp2 | a0001 | c0001 | t0019 | g0177 | AFR | USA | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18955 | hp1 | a0001 | c0001 | t0032 | g0004 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA18955 | hp2 | a0001 | c0001 | t0030 | g0005 | EAS | JPT | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | USA | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA20300 | hp2 | a0001 | c0001 | t0032 | g0031 | AFR | USA | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA21309 | hp1 | a0001 | c0001 | t0045 | g0015 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
NA21309 | hp2 | a0001 | c0003 | t0077 | g0113 | AFR | LWK | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
homoSapiens | chm13v2 | a0001 | c0001 | t0012 | g0118 | REF | REF | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0169 | REF | REF | AKAP11_chr13_42267152_42328261 | AKAP11 | chr13 | 42267152 | 42328261 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:42297145 | A | G | 1 | a0014 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.314A>G | p.Asn105Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/13 | 490/9915 | 314/5706 | 105/1901 | chr13 | 42297145 | |||
chr13:42298660 | T | C | 1 | a0020 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.479T>C | p.Leu160Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/13 | 655/9915 | 479/5706 | 160/1901 | chr13 | 42298660 | |||
chr13:42300231 | T | G | 1 | a0021 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1485T>G | p.Ile495Met | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 1661/9915 | 1485/5706 | 495/1901 | chr13 | 42300231 | |||
chr13:42300554 | G | A | 1 | a0014 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1808G>A | p.Arg603His | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 1984/9915 | 1808/5706 | 603/1901 | chr13 | 42300554 | |||
chr13:42300574 | C | T | 1 | a0004 | 3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.1828C>T | p.Arg610Cys | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2004/9915 | 1828/5706 | 610/1901 | chr13 | 42300574 | |||
chr13:42300908 | C | G | 1 | a0019 | 1 | NA18941.hp1 | missense_variant | MODERATE | c.2162C>G | p.Ser721Cys | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2338/9915 | 2162/5706 | 721/1901 | chr13 | 42300908 | |||
chr13:42300911 | C | T | 1 | a0018 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2165C>T | p.Thr722Met | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2341/9915 | 2165/5706 | 722/1901 | chr13 | 42300911 | |||
chr13:42300953 | C | T | 1 | a0010 | 2 | HG01256.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.2207C>T | p.Ser736Leu | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2383/9915 | 2207/5706 | 736/1901 | chr13 | 42300953 | |||
chr13:42300989 | A | G | 1 | a0022 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2243A>G | p.Asn748Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2419/9915 | 2243/5706 | 748/1901 | chr13 | 42300989 | |||
chr13:42301410 | A | T | 1 | a0013 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.2664A>T | p.Leu888Phe | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2840/9915 | 2664/5706 | 888/1901 | chr13 | 42301410 | |||
chr13:42301451 | A | G | 1 | a0009 | 2 | HG01123.hp1 HG02293.hp1 |
missense_variant | MODERATE | c.2705A>G | p.Glu902Gly | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2881/9915 | 2705/5706 | 902/1901 | chr13 | 42301451 | |||
chr13:42301454 | G | A | 1 | a0016 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.2708G>A | p.Arg903His | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2884/9915 | 2708/5706 | 903/1901 | chr13 | 42301454 | |||
chr13:42301547 | A | G | 1 | a0017 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.2801A>G | p.Asn934Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2977/9915 | 2801/5706 | 934/1901 | chr13 | 42301547 | |||
chr13:42301585 | A | G | 2 | a0003 a0007 |
13 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(10): Show |
missense_variant | MODERATE | c.2839A>G | p.Ile947Val | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3015/9915 | 2839/5706 | 947/1901 | chr13 | 42301585 | |||
chr13:42301834 | A | G | 1 | a0011 | 2 | HG01981.hp2 HG02647.hp2 |
missense_variant | MODERATE | c.3088A>G | p.Thr1030Ala | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3264/9915 | 3088/5706 | 1030/1901 | chr13 | 42301834 | |||
chr13:42301967 | C | T | 1 | a0002 | 17 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(14): Show |
missense_variant | MODERATE | c.3221C>T | p.Ser1074Phe | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3397/9915 | 3221/5706 | 1074/1901 | chr13 | 42301967 | |||
chr13:42301991 | G | T | 1 | a0006 | 3 | NA18945.hp2 NA18948.hp1 NA19056.hp1 |
missense_variant | MODERATE | c.3245G>T | p.Gly1082Val | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3421/9915 | 3245/5706 | 1082/1901 | chr13 | 42301991 | |||
chr13:42302074 | C | T | 1 | a0012 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.3328C>T | p.Arg1110Trp | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3504/9915 | 3328/5706 | 1110/1901 | chr13 | 42302074 | |||
chr13:42302479 | T | A | 1 | a0016 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.3733T>A | p.Phe1245Ile | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3909/9915 | 3733/5706 | 1245/1901 | chr13 | 42302479 | |||
chr13:42302725 | T | C | 1 | a0007 | 2 | HG00609.hp2 NA19085.hp1 |
missense_variant | MODERATE | c.3979T>C | p.Cys1327Arg | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4155/9915 | 3979/5706 | 1327/1901 | chr13 | 42302725 | |||
chr13:42302860 | G | A | 1 | a0015 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.4114G>A | p.Ala1372Thr | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4290/9915 | 4114/5706 | 1372/1901 | chr13 | 42302860 | |||
chr13:42302976 | A | C | 1 | a0005 | 3 | HG03098.hp2 HG03579.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.4230A>C | p.Leu1410Phe | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4406/9915 | 4230/5706 | 1410/1901 | chr13 | 42302976 | |||
chr13:42303004 | G | A | 1 | a0016 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.4258G>A | p.Glu1420Lys | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4434/9915 | 4258/5706 | 1420/1901 | chr13 | 42303004 | |||
chr13:42303121 | A | G | 1 | a0014 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.4375A>G | p.Thr1459Ala | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4551/9915 | 4375/5706 | 1459/1901 | chr13 | 42303121 | |||
chr13:42303572 | A | C | 1 | a0016 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.4826A>C | p.Gln1609Pro | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 5002/9915 | 4826/5706 | 1609/1901 | chr13 | 42303572 | |||
chr13:42303615 | T | G | 1 | a0013 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.4869T>G | p.Phe1623Leu | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 5045/9915 | 4869/5706 | 1623/1901 | chr13 | 42303615 | |||
chr13:42303622 | C | T | 1 | a0008 | 2 | HG01109.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.4876C>T | p.Arg1626Cys | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 5052/9915 | 4876/5706 | 1626/1901 | chr13 | 42303622 | |||
chr13:42303713 | C | T | 1 | a0023 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.4967C>T | p.Ala1656Val | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 5143/9915 | 4967/5706 | 1656/1901 | chr13 | 42303713 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:42298580 | A | G | 2 | a0001c0010 a0023c0029 |
4 | HG02148.hp2 NA18969.hp2 NA19062.hp1 others(1): Show |
synonymous_variant | LOW | c.399A>G | p.Ser133Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/13 | 575/9915 | 399/5706 | 133/1901 | chr13 | 42298580 | |||
chr13:42298583 | A | G | 6 | a0001c0002 a0001c0006 a0001c0026 others(3): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
synonymous_variant | LOW | c.402A>G | p.Pro134Pro | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/13 | 578/9915 | 402/5706 | 134/1901 | chr13 | 42298583 | |||
chr13:42298643 | C | T | 6 | a0001c0002 a0001c0006 a0001c0026 others(3): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
synonymous_variant | LOW | c.462C>T | p.Tyr154Tyr | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/13 | 638/9915 | 462/5706 | 154/1901 | chr13 | 42298643 | |||
chr13:42299646 | G | A | 1 | a0001c0006 | 4 | HG00642.hp1 HG00738.hp1 HG02698.hp1 others(1): Show |
synonymous_variant | LOW | c.900G>A | p.Ser300Ser | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 1076/9915 | 900/5706 | 300/1901 | chr13 | 42299646 | |||
chr13:42301122 | T | C | 1 | a0017c0017 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.2376T>C | p.Tyr792Tyr | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 2552/9915 | 2376/5706 | 792/1901 | chr13 | 42301122 | |||
chr13:42302154 | A | C | 3 | a0001c0003 a0009c0014 a0015c0020 |
30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
synonymous_variant | LOW | c.3408A>C | p.Thr1136Thr | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 3584/9915 | 3408/5706 | 1136/1901 | chr13 | 42302154 | |||
chr13:42303129 | G | C | 11 | a0001c0002 a0001c0006 a0001c0026 others(8): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
synonymous_variant | LOW | c.4383G>C | p.Leu1461Leu | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4559/9915 | 4383/5706 | 1461/1901 | chr13 | 42303129 | |||
chr13:42303252 | C | T | 1 | a0001c0026 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.4506C>T | p.His1502His | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4682/9915 | 4506/5706 | 1502/1901 | chr13 | 42303252 | |||
chr13:42303501 | A | G | 1 | a0003c0022 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.4755A>G | p.Gln1585Gln | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 4931/9915 | 4755/5706 | 1585/1901 | chr13 | 42303501 | |||
chr13:42303690 | A | G | 1 | a0001c0019 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.4944A>G | p.Ala1648Ala | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/13 | 5120/9915 | 4944/5706 | 1648/1901 | chr13 | 42303690 | |||
chr13:42308484 | C | T | 6 | a0001c0002 a0001c0006 a0001c0026 others(3): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
synonymous_variant | LOW | c.5148C>T | p.Thr1716Thr | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/13 | 5324/9915 | 5148/5706 | 1716/1901 | chr13 | 42308484 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:42272175 | C | T | 3 | a0001c0003t0093 a0001c0003t0094 a0015c0020t0095 |
3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-153C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/13 | chr13 | 42272175 | |||||||
chr13:42286333 | A | G | 1 | a0001c0001t0092 | 1 | HG01928.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-16A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/13 | chr13 | 42286333 | |||||||
chr13:42319338 | G | T | 2 | a0006c0008t0040 a0006c0008t0091 |
3 | NA18945.hp2 NA18948.hp1 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*110G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 110 | chr13 | 42319338 | ||||||
chr13:42319619 | T | C | 1 | a0017c0017t0041 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*391T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 391 | chr13 | 42319619 | ||||||
chr13:42319669 | A | T | 1 | a0001c0001t0090 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*441A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 441 | chr13 | 42319669 | ||||||
chr13:42319708 | C | CCTTT | 90 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(87): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*482_*485dupTTTC | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 486 | INFO_REALIGN_3_PRIME | chr13 | 42319708 | |||||
chr13:42319717 | T | C | 41 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(38): Show |
153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*489T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 489 | chr13 | 42319717 | ||||||
chr13:42319741 | A | T | 1 | a0001c0001t0071 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*513A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 513 | chr13 | 42319741 | ||||||
chr13:42319747 | C | T | 1 | a0001c0003t0089 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*519C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 519 | chr13 | 42319747 | ||||||
chr13:42319850 | C | T | 9 | a0001c0002t0001 a0001c0002t0017 a0001c0002t0087 others(6): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*622C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 622 | chr13 | 42319850 | ||||||
chr13:42319906 | G | GGT | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0012 others(11): Show |
54 | HG00140.hp1 HG00438.hp1 HG00733.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*721_*722dupGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | G | GGTGT | 8 | a0001c0001t0023 a0001c0001t0027 a0001c0001t0032 others(5): Show |
18 | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*719_*722dupGTGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | G | GGTGTGT | 6 | a0001c0001t0019 a0001c0001t0026 a0001c0001t0029 others(3): Show |
20 | HG00438.hp2 HG00609.hp1 HG01261.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*717_*722dupGTGTGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | G | GGTGTGTG others(1): Show |
10 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0020 others(7): Show |
37 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*715_*722dupGTGTGT others(2): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | G | GGTGTGTG others(3): Show |
7 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0021 others(4): Show |
39 | HG00140.hp2 HG00408.hp2 HG00735.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*713_*722dupGTGTGT others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | G | GGTGTGTG others(5): Show |
6 | a0001c0001t0003 a0001c0001t0024 a0001c0001t0037 others(3): Show |
25 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*711_*722dupGTGTGT others(6): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | G | GGTGTGTG others(7): Show |
4 | a0001c0001t0014 a0001c0001t0033 a0001c0001t0063 others(1): Show |
14 | HG00597.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*709_*722dupGTGTGT others(8): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | G | GGTGTGTG others(9): Show |
2 | a0001c0001t0066 a0021c0016t0065 |
2 | NA18951.hp1 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*707_*722dupGTGTGT others(10): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | G | GGTGTGTG others(11): Show |
2 | a0001c0001t0067 a0001c0001t0068 |
2 | HG02523.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*705_*722dupGTGTGT others(12): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | G | GGTGTGTG others(13): Show |
2 | a0001c0001t0069 a0001c0001t0070 |
2 | NA19030.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*703_*722dupGTGTGT others(14): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 723 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | GGT | G | 9 | a0001c0001t0013 a0001c0001t0015 a0001c0001t0018 others(6): Show |
39 | HG00323.hp1 HG00639.hp2 HG01256.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*721_*722delGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 721 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | GGTGT | G | 9 | a0001c0001t0011 a0001c0003t0022 a0001c0003t0025 others(6): Show |
25 | HG00423.hp1 HG01109.hp1 HG01123.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*719_*722delGTGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 719 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | GGTGTGT | G | 9 | a0001c0001t0031 a0001c0001t0052 a0001c0001t0053 others(6): Show |
30 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*717_*722delGTGTGT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 717 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | GGTGTGTG others(1): Show |
G | 9 | a0001c0002t0001 a0001c0002t0087 a0001c0006t0001 others(6): Show |
38 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*715_*722delGTGTGT others(2): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 715 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | GGTGTGTG others(3): Show |
G | 1 | a0003c0005t0075 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*713_*722delGTGTGT others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 713 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | GGTGTGTG others(11): Show |
G | 1 | a0001c0001t0051 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*705_*722delGTGTGT others(12): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 705 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | GGTGTGTG others(13): Show |
G | 1 | a0001c0001t0074 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*703_*722delGTGTGT others(14): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 703 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319906 | GGTGTGTG others(17): Show |
G | 1 | a0001c0001t0036 | 2 | HG02976.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*699_*722delGTGTGT others(18): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 699 | INFO_REALIGN_3_PRIME | chr13 | 42319906 | |||||
chr13:42319909 | G | A | 1 | a0004c0009t0073 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*681G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 681 | chr13 | 42319909 | ||||||
chr13:42319911 | G | A | 1 | a0004c0009t0072 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*683G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 683 | chr13 | 42319911 | ||||||
chr13:42319973 | AGTTT | A | 2 | a0001c0001t0012 a0012c0021t0012 |
8 | HG00140.hp1 HG00733.hp2 HG01243.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*749_*752delTGTT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 749 | INFO_REALIGN_3_PRIME | chr13 | 42319973 | |||||
chr13:42320002 | T | C | 1 | a0001c0001t0058 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 774 | chr13 | 42320002 | ||||||
chr13:42320061 | A | C | 1 | a0016c0018t0076 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*833A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 833 | chr13 | 42320061 | ||||||
chr13:42320099 | A | T | 1 | a0002c0004t0042 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*871A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 871 | chr13 | 42320099 | ||||||
chr13:42320100 | T | A | 1 | a0001c0003t0077 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*872T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 872 | chr13 | 42320100 | ||||||
chr13:42320131 | T | C | 1 | a0001c0001t0062 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*903T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 903 | chr13 | 42320131 | ||||||
chr13:42320151 | A | T | 9 | a0001c0002t0001 a0001c0002t0017 a0001c0002t0087 others(6): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*923A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 923 | chr13 | 42320151 | ||||||
chr13:42320232 | A | G | 41 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(38): Show |
153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*1004A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1004 | chr13 | 42320232 | ||||||
chr13:42320249 | T | C | 1 | a0001c0001t0043 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1021T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1021 | chr13 | 42320249 | ||||||
chr13:42320259 | G | A | 76 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(73): Show |
267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*1031G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1031 | chr13 | 42320259 | ||||||
chr13:42320262 | G | T | 1 | a0017c0017t0041 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1034G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1034 | chr13 | 42320262 | ||||||
chr13:42320269 | T | G | 1 | a0005c0007t0039 | 2 | HG03579.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1041T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1041 | chr13 | 42320269 | ||||||
chr13:42320269 | TTTTGTTT others(1): Show |
T | 18 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0009 others(15): Show |
74 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1057_*1064delGTTT others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1057 | INFO_REALIGN_3_PRIME | chr13 | 42320269 | |||||
chr13:42320273 | G | T | 11 | a0001c0001t0016 a0001c0001t0026 a0001c0001t0027 others(8): Show |
26 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1045G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1045 | chr13 | 42320273 | ||||||
chr13:42320277 | G | T | 1 | a0001c0001t0084 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1049G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1049 | chr13 | 42320277 | ||||||
chr13:42320278 | T | G | 1 | a0001c0001t0084 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1050T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1050 | chr13 | 42320278 | ||||||
chr13:42320321 | G | A | 1 | a0001c0001t0059 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1093G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1093 | chr13 | 42320321 | ||||||
chr13:42320341 | A | G | 3 | a0001c0003t0093 a0001c0003t0094 a0015c0020t0095 |
3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1113A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1113 | chr13 | 42320341 | ||||||
chr13:42320386 | C | G | 1 | a0001c0001t0046 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1158C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1158 | chr13 | 42320386 | ||||||
chr13:42320452 | C | A | 3 | a0004c0009t0072 a0004c0009t0073 a0004c0009t0080 |
3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1224C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1224 | chr13 | 42320452 | ||||||
chr13:42320491 | T | C | 1 | a0001c0001t0044 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1263T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1263 | chr13 | 42320491 | ||||||
chr13:42320508 | C | T | 1 | a0001c0003t0077 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1280C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1280 | chr13 | 42320508 | ||||||
chr13:42320671 | T | G | 2 | a0001c0002t0087 a0016c0018t0076 |
2 | HG03710.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1443T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1443 | chr13 | 42320671 | ||||||
chr13:42320817 | G | A | 1 | a0017c0017t0041 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1589G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1589 | chr13 | 42320817 | ||||||
chr13:42321030 | C | T | 76 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(73): Show |
267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*1802C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1802 | chr13 | 42321030 | ||||||
chr13:42321119 | T | G | 1 | a0014c0030t0083 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1891T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 1891 | chr13 | 42321119 | ||||||
chr13:42321407 | C | T | 1 | a0001c0001t0045 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2179C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2179 | chr13 | 42321407 | ||||||
chr13:42321434 | T | C | 1 | a0001c0002t0088 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2206T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2206 | chr13 | 42321434 | ||||||
chr13:42321456 | CACTT | C | 1 | a0001c0003t0025 | 6 | HG02109.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2231_*2234delTTAC | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2231 | INFO_REALIGN_3_PRIME | chr13 | 42321456 | |||||
chr13:42321458 | C | G | 1 | a0001c0001t0074 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2230C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2230 | chr13 | 42321458 | ||||||
chr13:42321462 | C | T | 1 | a0001c0001t0074 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2234C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2234 | chr13 | 42321462 | ||||||
chr13:42321592 | T | G | 15 | a0001c0002t0001 a0001c0002t0017 a0001c0002t0087 others(12): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2364T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2364 | chr13 | 42321592 | ||||||
chr13:42321703 | A | G | 1 | a0001c0002t0088 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2475A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2475 | chr13 | 42321703 | ||||||
chr13:42321856 | G | A | 10 | a0001c0003t0010 a0001c0003t0022 a0001c0003t0025 others(7): Show |
30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2628G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2628 | chr13 | 42321856 | ||||||
chr13:42321963 | T | C | 15 | a0001c0002t0001 a0001c0002t0017 a0001c0002t0087 others(12): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2735T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2735 | chr13 | 42321963 | ||||||
chr13:42322007 | T | C | 1 | a0001c0001t0052 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2779T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2779 | chr13 | 42322007 | ||||||
chr13:42322054 | A | G | 3 | a0001c0001t0055 a0001c0001t0057 a0001c0001t0058 |
3 | HG02809.hp2 HG02895.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2826A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2826 | chr13 | 42322054 | ||||||
chr13:42322081 | A | G | 1 | a0014c0030t0083 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2853A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 2853 | chr13 | 42322081 | ||||||
chr13:42322252 | T | G | 5 | a0003c0005t0008 a0003c0005t0075 a0003c0022t0008 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3024T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3024 | chr13 | 42322252 | ||||||
chr13:42322287 | A | G | 6 | a0001c0001t0021 a0001c0001t0029 a0001c0001t0030 others(3): Show |
19 | HG00438.hp2 HG00609.hp1 HG02165.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3059A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3059 | chr13 | 42322287 | ||||||
chr13:42322423 | A | G | 1 | a0001c0001t0031 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3195A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3195 | chr13 | 42322423 | ||||||
chr13:42322609 | A | T | 1 | a0001c0001t0085 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3381A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3381 | chr13 | 42322609 | ||||||
chr13:42322669 | T | G | 1 | a0003c0005t0075 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3441T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3441 | chr13 | 42322669 | ||||||
chr13:42322770 | T | C | 1 | a0001c0001t0063 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3542T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 13/13 | 3542 | chr13 | 42322770 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:42272302 | G | A | 23 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(20): Show |
45 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.-100+74G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272302 | |||||||
chr13:42272347 | C | G | 4 | a0003c0005t0008g0006 a0003c0022t0008g0199 a0007c0013t0008g0006 others(1): Show |
13 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-100+119C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272347 | |||||||
chr13:42272418 | G | A | 1 | a0001c0001t0071g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-100+190G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272418 | |||||||
chr13:42272527 | C | T | 1 | a0001c0001t0018g0198 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-100+299C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272527 | |||||||
chr13:42272570 | G | C | 5 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-100+342G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272570 | |||||||
chr13:42272587 | GCGTGGTG others(19): Show |
G | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-100+367_-100+392d others(28): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42272587 | ||||||
chr13:42272668 | C | T | 1 | a0001c0001t0003g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-100+440C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272668 | |||||||
chr13:42272878 | G | A | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-100+650G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272878 | |||||||
chr13:42272905 | C | T | 1 | a0001c0001t0005g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-100+677C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42272905 | |||||||
chr13:42273278 | T | A | 1 | a0003c0022t0008g0199 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-100+1050T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273278 | |||||||
chr13:42273298 | T | G | 90 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(87): Show |
117 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.-100+1070T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273298 | |||||||
chr13:42273357 | AT | A | 8 | a0001c0001t0009g0065 a0001c0001t0019g0064 a0001c0001t0026g0107 others(5): Show |
17 | HG00423.hp2 HG00609.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.-100+1143delT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42273357 | ||||||
chr13:42273592 | C | G | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-100+1364C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273592 | |||||||
chr13:42273689 | G | C | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-100+1461G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273689 | |||||||
chr13:42273724 | A | T | 1 | a0014c0030t0083g0194 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-100+1496A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273724 | |||||||
chr13:42273800 | T | A | 1 | a0001c0003t0077g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-100+1572T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273800 | |||||||
chr13:42273913 | T | G | 45 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0036 others(42): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-100+1685T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42273913 | |||||||
chr13:42274140 | G | T | 1 | a0001c0001t0004g0193 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-100+1912G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274140 | |||||||
chr13:42274292 | G | T | 1 | a0002c0004t0018g0137 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-100+2064G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274292 | |||||||
chr13:42274329 | C | T | 1 | a0001c0001t0015g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-100+2101C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274329 | |||||||
chr13:42274446 | G | A | 4 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(1): Show |
13 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-100+2218G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274446 | |||||||
chr13:42274470 | G | C | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-100+2242G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274470 | |||||||
chr13:42274510 | C | T | 116 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(113): Show |
153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-100+2282C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274510 | |||||||
chr13:42274511 | C | T | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-100+2283C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274511 | |||||||
chr13:42274663 | C | A | 146 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(143): Show |
193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-100+2435C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274663 | |||||||
chr13:42274663 | C | CGACTGAG others(63): Show |
1 | a0001c0001t0016g0158 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-100+2488_-100+248 others(74): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42274663 | ||||||
chr13:42274708 | T | C | 1 | a0001c0001t0085g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-100+2480T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274708 | |||||||
chr13:42274717 | G | A | 23 | a0001c0001t0016g0025 a0001c0001t0016g0044 a0001c0001t0016g0158 others(20): Show |
27 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.-100+2489G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274717 | |||||||
chr13:42274849 | T | G | 1 | a0001c0001t0043g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-100+2621T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274849 | |||||||
chr13:42274928 | C | A | 1 | a0013c0023t0078g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-100+2700C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42274928 | |||||||
chr13:42275005 | G | T | 3 | a0004c0009t0072g0173 a0004c0009t0073g0175 a0004c0009t0080g0174 |
3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-100+2777G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275005 | |||||||
chr13:42275079 | C | T | 1 | a0001c0003t0093g0157 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-100+2851C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275079 | |||||||
chr13:42275189 | A | G | 23 | a0001c0003t0010g0017 a0001c0003t0010g0023 a0001c0003t0010g0042 others(20): Show |
30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-100+2961A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275189 | |||||||
chr13:42275292 | A | G | 1 | a0001c0001t0004g0192 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-100+3064A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275292 | |||||||
chr13:42275369 | A | G | 116 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(113): Show |
153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-100+3141A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275369 | |||||||
chr13:42275414 | T | A | 2 | a0001c0001t0003g0019 a0001c0001t0014g0019 |
3 | NA18939.hp1 NA18947.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-100+3186T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275414 | |||||||
chr13:42275426 | A | G | 3 | a0001c0003t0025g0024 a0001c0003t0025g0155 a0001c0003t0025g0156 |
5 | HG02109.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100+3198A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275426 | |||||||
chr13:42275679 | C | T | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-100+3451C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275679 | |||||||
chr13:42275750 | C | A | 1 | a0016c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-100+3522C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275750 | |||||||
chr13:42275808 | G | A | 121 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(118): Show |
158 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.-100+3580G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275808 | |||||||
chr13:42275906 | T | G | 2 | a0001c0001t0002g0036 a0001c0001t0002g0115 |
3 | HG02155.hp1 NA18973.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-100+3678T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42275906 | |||||||
chr13:42276046 | T | G | 5 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-100+3818T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276046 | |||||||
chr13:42276404 | G | T | 3 | a0001c0001t0055g0190 a0001c0001t0057g0191 a0001c0001t0058g0189 |
3 | HG02809.hp2 HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-100+4176G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276404 | |||||||
chr13:42276484 | C | A | 1 | a0001c0001t0003g0066 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-100+4256C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276484 | |||||||
chr13:42276507 | A | G | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100+4279A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276507 | |||||||
chr13:42276564 | T | G | 1 | a0016c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-100+4336T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276564 | |||||||
chr13:42276675 | A | G | 1 | a0001c0019t0081g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-100+4447A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276675 | |||||||
chr13:42276713 | T | C | 23 | a0001c0001t0016g0025 a0001c0001t0016g0044 a0001c0001t0016g0158 others(20): Show |
27 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.-100+4485T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276713 | |||||||
chr13:42276894 | T | C | 1 | a0001c0001t0013g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-100+4666T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276894 | |||||||
chr13:42276923 | G | C | 1 | a0001c0001t0023g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-100+4695G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42276923 | |||||||
chr13:42277013 | G | T | 1 | a0001c0001t0014g0105 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-100+4785G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277013 | |||||||
chr13:42277034 | A | T | 2 | a0002c0004t0011g0041 a0002c0004t0011g0136 |
3 | HG02015.hp1 NA18979.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-100+4806A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277034 | |||||||
chr13:42277070 | T | C | 2 | a0001c0001t0005g0029 a0001c0001t0019g0029 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-100+4842T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277070 | |||||||
chr13:42277070 | T | G | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-100+4842T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277070 | |||||||
chr13:42277135 | A | G | 35 | a0001c0001t0003g0010 a0001c0001t0006g0010 a0001c0001t0009g0010 others(32): Show |
68 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-100+4907A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277135 | |||||||
chr13:42277138 | T | C | 1 | a0014c0030t0083g0194 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-100+4910T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277138 | |||||||
chr13:42277198 | A | C | 184 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(181): Show |
267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.-100+4970A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277198 | |||||||
chr13:42277364 | A | G | 1 | a0001c0003t0010g0043 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-100+5136A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277364 | |||||||
chr13:42277572 | G | A | 11 | a0001c0001t0002g0015 a0001c0001t0002g0037 a0001c0001t0002g0120 others(8): Show |
19 | HG00140.hp1 HG00733.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-100+5344G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277572 | |||||||
chr13:42277653 | G | A | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-100+5425G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277653 | |||||||
chr13:42277727 | G | A | 23 | a0001c0003t0010g0017 a0001c0003t0010g0023 a0001c0003t0010g0042 others(20): Show |
30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-100+5499G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277727 | |||||||
chr13:42277747 | A | G | 2 | a0001c0001t0013g0067 a0001c0001t0028g0104 |
2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-100+5519A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277747 | |||||||
chr13:42277903 | T | C | 9 | a0001c0001t0004g0004 a0001c0001t0004g0047 a0001c0001t0004g0192 others(6): Show |
19 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-100+5675T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277903 | |||||||
chr13:42277972 | A | G | 1 | a0001c0001t0028g0188 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-100+5744A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42277972 | |||||||
chr13:42278163 | C | G | 3 | a0001c0003t0025g0024 a0001c0003t0025g0155 a0001c0003t0025g0156 |
5 | HG02109.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-100+5935C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278163 | |||||||
chr13:42278284 | C | T | 3 | a0001c0003t0093g0157 a0001c0003t0094g0153 a0015c0020t0095g0154 |
3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-100+6056C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278284 | |||||||
chr13:42278376 | A | C | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6148A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278376 | |||||||
chr13:42278377 | G | C | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6149G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278377 | |||||||
chr13:42278378 | G | T | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6150G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278378 | |||||||
chr13:42278379 | A | T | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6151A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278379 | |||||||
chr13:42278380 | A | T | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6152A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278380 | |||||||
chr13:42278384 | A | G | 1 | a0001c0002t0001g0061 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-100+6156A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278384 | |||||||
chr13:42278755 | G | A | 1 | a0001c0001t0009g0068 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-100+6527G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278755 | |||||||
chr13:42278853 | C | T | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-100+6625C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278853 | |||||||
chr13:42278931 | C | T | 1 | a0001c0001t0028g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-100+6703C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278931 | |||||||
chr13:42278931 | CT | C | 3 | a0001c0001t0007g0008 a0001c0001t0007g0122 a0001c0001t0014g0105 |
9 | NA18946.hp1 NA18959.hp1 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.-100+6715delT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42278931 | ||||||
chr13:42278941 | T | C | 1 | a0001c0002t0017g0050 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-100+6713T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278941 | |||||||
chr13:42278982 | T | C | 1 | a0016c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-100+6754T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278982 | |||||||
chr13:42278989 | C | T | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-100+6761C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42278989 | |||||||
chr13:42279005 | G | A | 1 | a0001c0001t0079g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-100+6777G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279005 | |||||||
chr13:42279169 | A | G | 1 | a0001c0001t0006g0103 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-99-6817A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279169 | |||||||
chr13:42279216 | T | TA | 184 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(181): Show |
267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.-99-6770_-99-6769i others(3): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279216 | |||||||
chr13:42279263 | C | CCA | 63 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0036 others(60): Show |
95 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-99-6705_-99-6704d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279263 | ||||||
chr13:42279263 | C | CCACACA | 22 | a0001c0002t0001g0001 a0001c0002t0001g0027 a0001c0002t0001g0028 others(19): Show |
43 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-99-6709_-99-6704d others(8): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279263 | ||||||
chr13:42279263 | C | CCACACAC others(1): Show |
2 | a0001c0002t0001g0026 a0001c0002t0001g0052 |
3 | HG01515.hp1 HG01517.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-99-6711_-99-6704d others(10): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279263 | ||||||
chr13:42279263 | CCA | C | 4 | a0001c0001t0005g0029 a0001c0001t0019g0029 a0001c0001t0062g0100 others(1): Show |
4 | HG02602.hp2 HG02698.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99-6705_-99-6704d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279263 | ||||||
chr13:42279265 | A | C | 1 | a0001c0001t0024g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-99-6721A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279265 | |||||||
chr13:42279281 | A | ACT | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-99-6693_-99-6692d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279281 | ||||||
chr13:42279281 | A | T | 2 | a0001c0001t0006g0101 a0016c0018t0076g0106 |
2 | HG00140.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-99-6705A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279281 | |||||||
chr13:42279281 | ACT | A | 3 | a0005c0007t0034g0142 a0005c0007t0039g0140 a0005c0007t0039g0141 |
3 | HG03098.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-99-6693_-99-6692d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279281 | ||||||
chr13:42279283 | T | A | 35 | a0001c0002t0088g0051 a0001c0003t0010g0017 a0001c0003t0010g0023 others(32): Show |
48 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-99-6703T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279283 | |||||||
chr13:42279285 | T | A | 22 | a0001c0003t0010g0017 a0001c0003t0010g0023 a0001c0003t0010g0042 others(19): Show |
29 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-99-6701T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279285 | |||||||
chr13:42279287 | T | A | 3 | a0001c0003t0093g0157 a0001c0003t0094g0153 a0015c0020t0095g0154 |
3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-99-6699T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279287 | |||||||
chr13:42279291 | TCTCA | T | 3 | a0001c0001t0055g0190 a0001c0001t0057g0191 a0001c0001t0058g0189 |
3 | HG02809.hp2 HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-99-6683_-99-6680d others(6): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279291 | ||||||
chr13:42279293 | TCA | T | 10 | a0002c0004t0007g0124 a0002c0004t0007g0127 a0002c0004t0011g0011 others(7): Show |
16 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.-99-6691_-99-6690d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42279293 | ||||||
chr13:42279295 | A | T | 24 | a0001c0003t0010g0017 a0001c0003t0010g0023 a0001c0003t0010g0042 others(21): Show |
31 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.-99-6691A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279295 | |||||||
chr13:42279307 | G | T | 1 | a0001c0003t0022g0150 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-99-6679G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279307 | |||||||
chr13:42279351 | T | C | 5 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-99-6635T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279351 | |||||||
chr13:42279371 | C | T | 1 | a0001c0001t0019g0186 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-99-6615C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279371 | |||||||
chr13:42279504 | G | A | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-99-6482G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279504 | |||||||
chr13:42279535 | G | A | 2 | a0001c0003t0010g0023 a0001c0003t0010g0143 |
4 | HG00323.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99-6451G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279535 | |||||||
chr13:42279615 | A | G | 24 | a0001c0001t0031g0016 a0001c0003t0010g0017 a0001c0003t0010g0023 others(21): Show |
34 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-99-6371A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279615 | |||||||
chr13:42279767 | T | A | 1 | a0009c0014t0022g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-99-6219T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279767 | |||||||
chr13:42279855 | G | A | 210 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(207): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.-99-6131G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279855 | |||||||
chr13:42279911 | C | T | 3 | a0005c0007t0034g0142 a0005c0007t0039g0140 a0005c0007t0039g0141 |
3 | HG03098.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-99-6075C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279911 | |||||||
chr13:42279926 | T | C | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-99-6060T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42279926 | |||||||
chr13:42280208 | C | T | 1 | a0001c0001t0090g0167 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-99-5778C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280208 | |||||||
chr13:42280231 | C | T | 1 | a0001c0002t0001g0028 | 2 | HG00597.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-99-5755C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280231 | |||||||
chr13:42280392 | A | G | 1 | a0001c0001t0021g0099 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-99-5594A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280392 | |||||||
chr13:42280476 | C | T | 1 | a0001c0001t0033g0098 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-99-5510C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280476 | |||||||
chr13:42280503 | A | G | 210 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(207): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.-99-5483A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280503 | |||||||
chr13:42280537 | C | A | 3 | a0001c0001t0006g0069 a0001c0001t0006g0071 a0001c0001t0061g0070 |
3 | HG00741.hp1 HG01261.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-99-5449C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280537 | |||||||
chr13:42280546 | T | C | 1 | a0016c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-99-5440T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280546 | |||||||
chr13:42280798 | T | C | 4 | a0001c0001t0003g0013 a0001c0001t0006g0013 a0001c0001t0009g0013 others(1): Show |
5 | HG00642.hp2 HG01346.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.-99-5188T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280798 | |||||||
chr13:42280957 | T | C | 3 | a0001c0001t0002g0036 a0001c0001t0002g0115 a0001c0001t0002g0128 |
4 | HG02155.hp1 NA18973.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99-5029T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42280957 | |||||||
chr13:42281293 | G | C | 30 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(27): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-99-4693G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42281293 | |||||||
chr13:42281468 | C | A | 30 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(27): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-99-4518C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42281468 | |||||||
chr13:42281980 | C | CT | 43 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0036 others(40): Show |
74 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-99-3990dupT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42281980 | ||||||
chr13:42281983 | T | TC | 9 | a0001c0001t0003g0009 a0001c0001t0003g0013 a0001c0001t0003g0066 others(6): Show |
13 | HG00642.hp2 HG01346.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-99-4003_-99-4002i others(3): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42281983 | |||||||
chr13:42281984 | T | C | 107 | a0001c0001t0003g0002 a0001c0001t0003g0010 a0001c0001t0003g0019 others(104): Show |
140 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.-99-4002T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42281984 | |||||||
chr13:42282008 | G | A | 1 | a0001c0001t0006g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-99-3978G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282008 | |||||||
chr13:42282102 | G | A | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-99-3884G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282102 | |||||||
chr13:42282104 | G | A | 116 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(113): Show |
153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-99-3882G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282104 | |||||||
chr13:42282260 | C | CT | 11 | a0001c0001t0004g0047 a0001c0001t0004g0193 a0001c0001t0007g0008 others(8): Show |
18 | HG01496.hp1 HG02056.hp2 HG02135.hp1 others(15): Show |
intron_variant | MODIFIER | c.-99-3704dupT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42282260 | ||||||
chr13:42282260 | C | CTT | 5 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-99-3705_-99-3704d others(4): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42282260 | ||||||
chr13:42282260 | CT | C | 29 | a0001c0001t0015g0109 a0001c0001t0021g0030 a0001c0001t0026g0107 others(26): Show |
51 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.-99-3704delT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42282260 | ||||||
chr13:42282308 | A | T | 256 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0036 others(253): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.-99-3678A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282308 | |||||||
chr13:42282489 | T | C | 145 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(142): Show |
192 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.-99-3497T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282489 | |||||||
chr13:42282562 | A | T | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-99-3424A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282562 | |||||||
chr13:42282669 | A | G | 6 | a0001c0001t0005g0029 a0001c0001t0019g0029 a0001c0001t0062g0100 others(3): Show |
6 | HG02602.hp2 HG02698.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99-3317A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42282669 | |||||||
chr13:42283115 | C | G | 1 | a0001c0001t0002g0037 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-99-2871C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283115 | |||||||
chr13:42283144 | C | T | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-99-2842C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283144 | |||||||
chr13:42283146 | C | T | 2 | a0001c0001t0052g0049 a0001c0001t0053g0049 |
2 | HG01243.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-99-2840C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283146 | |||||||
chr13:42283360 | CA | C | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-99-2625delA | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283360 | |||||||
chr13:42283385 | A | G | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.-99-2601A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283385 | |||||||
chr13:42283436 | G | A | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-99-2550G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283436 | |||||||
chr13:42283651 | A | G | 4 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(1): Show |
13 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-99-2335A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283651 | |||||||
chr13:42283765 | A | C | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-99-2221A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283765 | |||||||
chr13:42283830 | G | A | 1 | a0016c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-99-2156G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42283830 | |||||||
chr13:42284001 | G | A | 11 | a0002c0004t0007g0123 a0002c0004t0007g0124 a0002c0004t0007g0127 others(8): Show |
17 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.-99-1985G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284001 | |||||||
chr13:42284028 | A | G | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.-99-1958A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284028 | |||||||
chr13:42284130 | G | A | 2 | a0009c0014t0022g0151 a0009c0014t0022g0152 |
2 | HG01123.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-99-1856G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284130 | |||||||
chr13:42284254 | T | C | 11 | a0002c0004t0007g0123 a0002c0004t0007g0124 a0002c0004t0007g0127 others(8): Show |
17 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.-99-1732T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284254 | |||||||
chr13:42284331 | C | T | 1 | a0001c0001t0015g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-99-1655C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284331 | |||||||
chr13:42284644 | CA | C | 4 | a0001c0001t0013g0183 a0001c0001t0013g0185 a0008c0011t0011g0117 others(1): Show |
4 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99-1339delA | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42284644 | ||||||
chr13:42284714 | A | G | 1 | a0001c0001t0074g0139 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-99-1272A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42284714 | |||||||
chr13:42285433 | A | G | 1 | a0002c0004t0007g0127 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-99-553A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285433 | |||||||
chr13:42285543 | T | C | 1 | a0001c0001t0020g0072 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-99-443T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285543 | |||||||
chr13:42285788 | T | TATATTTG others(9): Show |
1 | a0001c0006t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-99-196_-99-195ins others(16): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42285788 | ||||||
chr13:42285791 | C | T | 1 | a0001c0006t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-99-195C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285791 | |||||||
chr13:42285793 | A | G | 1 | a0001c0006t0001g0053 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-99-193A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285793 | |||||||
chr13:42285805 | A | G | 184 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(181): Show |
267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.-99-181A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285805 | |||||||
chr13:42285819 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-99-167C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285819 | |||||||
chr13:42285869 | C | CATAGAGA others(4): Show |
1 | a0001c0001t0013g0182 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-99-116_-99-115ins others(11): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42285869 | ||||||
chr13:42285871 | C | G | 1 | a0001c0001t0013g0182 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-99-115C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285871 | |||||||
chr13:42285882 | G | A | 1 | a0001c0001t0058g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-99-104G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | chr13 | 42285882 | |||||||
chr13:42285905 | A | AG | 23 | a0001c0003t0010g0017 a0001c0003t0010g0023 a0001c0003t0010g0042 others(20): Show |
30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-99-78dupG | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 42285905 | ||||||
chr13:42286038 | A | G | 1 | a0005c0007t0034g0142 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.-50+3A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 2/12 | chr13 | 42286038 | |||||||
chr13:42286559 | A | G | 1 | a0001c0001t0074g0139 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.51+160A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42286559 | |||||||
chr13:42286601 | G | A | 1 | a0001c0001t0062g0100 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.51+202G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42286601 | |||||||
chr13:42286834 | G | A | 1 | a0001c0001t0047g0130 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.51+435G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42286834 | |||||||
chr13:42286901 | C | A | 1 | a0014c0030t0083g0194 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.51+502C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42286901 | |||||||
chr13:42286941 | G | T | 3 | a0001c0001t0020g0021 a0001c0001t0067g0021 a0001c0001t0069g0021 |
3 | HG03486.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.51+542G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42286941 | |||||||
chr13:42287111 | C | T | 1 | a0001c0019t0081g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.51+712C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287111 | |||||||
chr13:42287209 | A | G | 1 | a0001c0003t0022g0149 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.51+810A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287209 | |||||||
chr13:42287228 | C | T | 30 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(27): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.51+829C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287228 | |||||||
chr13:42287290 | T | A | 2 | a0001c0001t0005g0073 a0001c0001t0005g0074 |
2 | HG01074.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.51+891T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287290 | |||||||
chr13:42287300 | T | C | 3 | a0004c0009t0072g0173 a0004c0009t0073g0175 a0004c0009t0080g0174 |
3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.51+901T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287300 | |||||||
chr13:42287301 | T | G | 2 | a0001c0001t0028g0188 a0017c0017t0041g0197 |
2 | HG03225.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.51+902T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287301 | |||||||
chr13:42287475 | G | A | 120 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(117): Show |
157 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.51+1076G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287475 | |||||||
chr13:42287486 | G | A | 26 | a0001c0001t0016g0025 a0001c0001t0016g0044 a0001c0001t0016g0158 others(23): Show |
30 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.51+1087G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287486 | |||||||
chr13:42287536 | G | A | 45 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0036 others(42): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.51+1137G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287536 | |||||||
chr13:42287575 | C | T | 1 | a0001c0001t0015g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.51+1176C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287575 | |||||||
chr13:42287576 | G | T | 1 | a0001c0001t0033g0093 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.51+1177G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287576 | |||||||
chr13:42287626 | A | AT | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.51+1229dupT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr13 | 42287626 | ||||||
chr13:42287636 | A | C | 27 | a0001c0001t0016g0025 a0001c0001t0016g0044 a0001c0001t0016g0158 others(24): Show |
31 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.51+1237A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287636 | |||||||
chr13:42287714 | T | C | 3 | a0001c0003t0093g0157 a0001c0003t0094g0153 a0015c0020t0095g0154 |
3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.51+1315T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287714 | |||||||
chr13:42287813 | T | C | 1 | a0001c0001t0061g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.51+1414T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287813 | |||||||
chr13:42287883 | C | T | 1 | a0001c0001t0019g0186 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+1484C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42287883 | |||||||
chr13:42288113 | A | G | 3 | a0001c0010t0016g0045 a0001c0010t0027g0046 a0023c0029t0026g0045 |
4 | HG02148.hp2 NA18969.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.51+1714A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288113 | |||||||
chr13:42288119 | A | G | 1 | a0001c0001t0020g0092 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.51+1720A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288119 | |||||||
chr13:42288287 | C | T | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.51+1888C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288287 | |||||||
chr13:42288422 | T | G | 1 | a0001c0003t0025g0145 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.51+2023T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288422 | |||||||
chr13:42288425 | A | G | 1 | a0001c0001t0079g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.51+2026A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288425 | |||||||
chr13:42288637 | CT | C | 7 | a0002c0004t0007g0123 a0002c0004t0007g0124 a0002c0004t0011g0011 others(4): Show |
13 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.51+2239delT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288637 | |||||||
chr13:42288736 | A | C | 5 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.51+2337A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288736 | |||||||
chr13:42288780 | T | A | 1 | a0002c0004t0042g0125 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.51+2381T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288780 | |||||||
chr13:42288813 | T | G | 8 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(5): Show |
13 | HG01975.hp2 HG01981.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.51+2414T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288813 | |||||||
chr13:42288902 | G | T | 1 | a0001c0001t0019g0186 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+2503G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288902 | |||||||
chr13:42288909 | A | C | 2 | a0001c0001t0074g0139 a0001c0001t0085g0138 |
2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.51+2510A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42288909 | |||||||
chr13:42289103 | T | C | 4 | a0001c0003t0025g0024 a0001c0003t0025g0145 a0001c0003t0025g0155 others(1): Show |
6 | HG02109.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.51+2704T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289103 | |||||||
chr13:42289222 | T | G | 1 | a0001c0001t0026g0168 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.51+2823T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289222 | |||||||
chr13:42289425 | T | G | 1 | a0001c0001t0016g0160 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.52-2960T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289425 | |||||||
chr13:42289498 | T | G | 30 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(27): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.52-2887T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289498 | |||||||
chr13:42289526 | C | G | 1 | a0010c0015t0013g0181 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.52-2859C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289526 | |||||||
chr13:42289558 | C | T | 9 | a0001c0003t0010g0017 a0001c0003t0010g0043 a0001c0003t0022g0144 others(6): Show |
11 | HG00099.hp1 HG00639.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.52-2827C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289558 | |||||||
chr13:42289616 | T | C | 30 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(27): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.52-2769T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289616 | |||||||
chr13:42289770 | C | T | 2 | a0001c0001t0016g0025 a0001c0001t0026g0025 |
3 | HG01106.hp2 HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.52-2615C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289770 | |||||||
chr13:42289820 | C | G | 5 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.52-2565C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42289820 | |||||||
chr13:42290330 | C | T | 1 | a0001c0001t0024g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.52-2055C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290330 | |||||||
chr13:42290457 | T | C | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.52-1928T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290457 | |||||||
chr13:42290526 | C | T | 1 | a0001c0001t0019g0091 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.52-1859C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290526 | |||||||
chr13:42290601 | T | G | 1 | a0005c0007t0039g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.52-1784T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290601 | |||||||
chr13:42290717 | A | G | 3 | a0001c0001t0020g0021 a0001c0001t0067g0021 a0001c0001t0069g0021 |
3 | HG03486.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.52-1668A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290717 | |||||||
chr13:42290774 | A | G | 1 | a0001c0001t0019g0091 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.52-1611A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290774 | |||||||
chr13:42290893 | T | C | 2 | a0006c0008t0040g0022 a0006c0008t0091g0022 |
3 | NA18945.hp2 NA18948.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.52-1492T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290893 | |||||||
chr13:42290932 | C | G | 184 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(181): Show |
267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.52-1453C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42290932 | |||||||
chr13:42291012 | G | A | 1 | a0011c0012t0034g0035 | 2 | HG01981.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.52-1373G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291012 | |||||||
chr13:42291050 | C | T | 1 | a0004c0009t0080g0174 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52-1335C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291050 | |||||||
chr13:42291061 | C | G | 23 | a0001c0003t0010g0017 a0001c0003t0010g0023 a0001c0003t0010g0042 others(20): Show |
30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.52-1324C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291061 | |||||||
chr13:42291378 | G | A | 1 | a0005c0007t0034g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.52-1007G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291378 | |||||||
chr13:42291400 | G | A | 11 | a0002c0004t0007g0123 a0002c0004t0007g0124 a0002c0004t0007g0127 others(8): Show |
17 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.52-985G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291400 | |||||||
chr13:42291415 | G | A | 5 | a0001c0001t0003g0010 a0001c0001t0006g0010 a0001c0001t0009g0010 others(2): Show |
7 | HG01928.hp2 HG03834.hp2 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.52-970G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291415 | |||||||
chr13:42291454 | T | G | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-931T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291454 | |||||||
chr13:42291527 | G | A | 45 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0036 others(42): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.52-858G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291527 | |||||||
chr13:42291926 | T | G | 1 | a0005c0007t0034g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.52-459T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42291926 | |||||||
chr13:42292015 | C | T | 1 | a0001c0001t0047g0130 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.52-370C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292015 | |||||||
chr13:42292045 | C | T | 121 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(118): Show |
158 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.52-340C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292045 | |||||||
chr13:42292047 | G | A | 30 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(27): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.52-338G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292047 | |||||||
chr13:42292106 | A | T | 3 | a0001c0001t0006g0020 a0001c0001t0014g0020 a0001c0001t0070g0020 |
3 | NA18961.hp2 NA18984.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.52-279A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292106 | |||||||
chr13:42292134 | A | T | 3 | a0001c0001t0006g0020 a0001c0001t0014g0020 a0001c0001t0070g0020 |
3 | NA18961.hp2 NA18984.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.52-251A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292134 | |||||||
chr13:42292204 | A | G | 3 | a0004c0009t0072g0173 a0004c0009t0073g0175 a0004c0009t0080g0174 |
3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.52-181A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292204 | |||||||
chr13:42292253 | G | A | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.52-132G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292253 | |||||||
chr13:42292282 | A | G | 1 | a0019c0028t0001g0059 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.52-103A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292282 | |||||||
chr13:42292324 | C | G | 1 | a0001c0001t0085g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52-61C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292324 | |||||||
chr13:42292346 | A | G | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-39A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 3/12 | chr13 | 42292346 | |||||||
chr13:42292609 | G | A | 1 | a0001c0001t0047g0130 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.168+108G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42292609 | |||||||
chr13:42292654 | GA | G | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.168+161delA | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr13 | 42292654 | ||||||
chr13:42292659 | A | G | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.168+158A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42292659 | |||||||
chr13:42292858 | A | G | 1 | a0001c0001t0035g0165 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.168+357A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42292858 | |||||||
chr13:42292973 | A | G | 1 | a0001c0001t0013g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.168+472A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42292973 | |||||||
chr13:42292981 | A | G | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.168+480A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42292981 | |||||||
chr13:42293417 | C | T | 1 | a0001c0003t0010g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.168+916C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293417 | |||||||
chr13:42293714 | G | A | 1 | a0001c0001t0020g0075 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.168+1213G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293714 | |||||||
chr13:42293750 | C | T | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.168+1249C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293750 | |||||||
chr13:42293818 | A | G | 147 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(144): Show |
194 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.168+1317A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293818 | |||||||
chr13:42293830 | T | G | 1 | a0001c0001t0035g0165 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.168+1329T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293830 | |||||||
chr13:42293842 | G | A | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+1341G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293842 | |||||||
chr13:42293844 | G | T | 1 | a0005c0007t0039g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.168+1343G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293844 | |||||||
chr13:42293962 | G | C | 256 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0036 others(253): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.168+1461G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42293962 | |||||||
chr13:42294005 | A | G | 1 | a0001c0001t0090g0167 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.168+1504A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294005 | |||||||
chr13:42294031 | A | G | 1 | a0001c0003t0025g0155 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.168+1530A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294031 | |||||||
chr13:42294072 | C | A | 23 | a0001c0001t0016g0025 a0001c0001t0016g0044 a0001c0001t0016g0158 others(20): Show |
27 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.168+1571C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294072 | |||||||
chr13:42294444 | C | G | 2 | a0001c0001t0013g0067 a0001c0001t0028g0104 |
2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.169-1251C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294444 | |||||||
chr13:42294476 | C | A | 1 | a0001c0001t0013g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.169-1219C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294476 | |||||||
chr13:42294572 | T | G | 23 | a0001c0001t0016g0025 a0001c0001t0016g0044 a0001c0001t0016g0158 others(20): Show |
27 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.169-1123T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294572 | |||||||
chr13:42294601 | A | C | 2 | a0001c0003t0022g0148 a0001c0003t0022g0150 |
2 | HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.169-1094A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294601 | |||||||
chr13:42294698 | G | A | 2 | a0001c0001t0032g0031 a0001c0001t0056g0031 |
2 | HG03491.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.169-997G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294698 | |||||||
chr13:42294748 | A | C | 1 | a0001c0001t0002g0120 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.169-947A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294748 | |||||||
chr13:42294983 | A | G | 23 | a0001c0001t0016g0025 a0001c0001t0016g0044 a0001c0001t0016g0158 others(20): Show |
27 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.169-712A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42294983 | |||||||
chr13:42295080 | A | G | 1 | a0001c0001t0011g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.169-615A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42295080 | |||||||
chr13:42295145 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.169-550G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42295145 | |||||||
chr13:42295349 | G | A | 3 | a0001c0001t0016g0160 a0001c0001t0016g0161 a0001c0001t0016g0162 |
3 | HG00099.hp2 HG01099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.169-346G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42295349 | |||||||
chr13:42295562 | T | C | 5 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.169-133T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | chr13 | 42295562 | |||||||
chr13:42295584 | A | AG | 184 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(181): Show |
267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.169-110dupG | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr13 | 42295584 | ||||||
chr13:42295874 | C | T | 30 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(27): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.216+132C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42295874 | |||||||
chr13:42295880 | G | A | 2 | a0001c0003t0022g0144 a0001c0003t0022g0147 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.216+138G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42295880 | |||||||
chr13:42296123 | C | G | 116 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(113): Show |
153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.216+381C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296123 | |||||||
chr13:42296185 | A | G | 2 | a0001c0001t0090g0167 a0001c0002t0001g0058 |
2 | HG01081.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.216+443A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296185 | |||||||
chr13:42296205 | A | G | 1 | a0001c0019t0081g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.216+463A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296205 | |||||||
chr13:42296277 | G | A | 256 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0036 others(253): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.216+535G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296277 | |||||||
chr13:42296395 | A | T | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.216+653A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296395 | |||||||
chr13:42296548 | C | T | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.217-500C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296548 | |||||||
chr13:42296667 | A | G | 30 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(27): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.217-381A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296667 | |||||||
chr13:42296713 | AAAGTT | A | 51 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0036 others(48): Show |
91 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.217-326_217-322del others(5): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 42296713 | ||||||
chr13:42296837 | G | A | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.217-211G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 5/12 | chr13 | 42296837 | |||||||
chr13:42297288 | A | G | 1 | a0003c0005t0075g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.351+106A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297288 | |||||||
chr13:42297326 | A | G | 1 | a0001c0001t0003g0066 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.351+144A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297326 | |||||||
chr13:42297367 | G | C | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.351+185G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297367 | |||||||
chr13:42297543 | C | T | 1 | a0001c0001t0023g0134 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.351+361C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297543 | |||||||
chr13:42297624 | TTTATAAA others(8): Show |
T | 1 | a0001c0001t0005g0077 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.351+446_351+460del others(15): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 42297624 | ||||||
chr13:42297738 | T | G | 1 | a0001c0003t0010g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.351+556T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297738 | |||||||
chr13:42297768 | C | A | 1 | a0001c0001t0029g0078 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.351+586C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297768 | |||||||
chr13:42297844 | C | G | 1 | a0001c0001t0085g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.351+662C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297844 | |||||||
chr13:42297888 | A | ATTTAC | 211 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(208): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.352-642_352-641ins others(5): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 42297888 | ||||||
chr13:42297989 | T | C | 1 | a0001c0001t0014g0032 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.352-544T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42297989 | |||||||
chr13:42298127 | G | A | 1 | a0002c0004t0007g0124 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.352-406G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42298127 | |||||||
chr13:42298189 | A | G | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.352-344A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42298189 | |||||||
chr13:42298515 | T | C | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-18T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 6/12 | chr13 | 42298515 | |||||||
chr13:42299028 | C | T | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.616+231C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/12 | chr13 | 42299028 | |||||||
chr13:42299212 | A | G | 1 | a0001c0001t0016g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.617-151A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/12 | chr13 | 42299212 | |||||||
chr13:42299218 | A | C | 1 | a0014c0030t0083g0194 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.617-145A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 7/12 | chr13 | 42299218 | |||||||
chr13:42304242 | A | T | 1 | a0001c0001t0024g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.5117+379A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304242 | |||||||
chr13:42304256 | C | T | 76 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(73): Show |
102 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.5117+393C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304256 | |||||||
chr13:42304305 | A | G | 1 | a0001c0001t0003g0090 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.5117+442A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304305 | |||||||
chr13:42304354 | A | G | 6 | a0002c0004t0007g0123 a0002c0004t0007g0124 a0002c0004t0011g0011 others(3): Show |
11 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.5117+491A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304354 | |||||||
chr13:42304423 | G | A | 1 | a0001c0003t0094g0153 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5117+560G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304423 | |||||||
chr13:42304486 | A | G | 2 | a0010c0015t0013g0181 a0010c0015t0028g0179 |
2 | HG01256.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5117+623A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304486 | |||||||
chr13:42304619 | C | T | 1 | a0001c0001t0019g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5117+756C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304619 | |||||||
chr13:42304620 | T | G | 1 | a0001c0001t0019g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5117+757T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304620 | |||||||
chr13:42304621 | C | A | 1 | a0001c0001t0019g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5117+758C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304621 | |||||||
chr13:42304622 | T | A | 1 | a0001c0001t0019g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5117+759T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304622 | |||||||
chr13:42304644 | T | C | 3 | a0005c0007t0034g0142 a0005c0007t0039g0140 a0005c0007t0039g0141 |
3 | HG03098.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5117+781T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304644 | |||||||
chr13:42304755 | C | CT | 32 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(29): Show |
62 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.5117+905dupT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 42304755 | ||||||
chr13:42304907 | C | T | 5 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.5117+1044C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42304907 | |||||||
chr13:42305030 | C | T | 2 | a0001c0001t0005g0029 a0001c0001t0019g0029 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.5117+1167C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305030 | |||||||
chr13:42305094 | G | C | 184 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(181): Show |
267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.5117+1231G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305094 | |||||||
chr13:42305158 | A | G | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.5117+1295A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305158 | |||||||
chr13:42305213 | T | C | 23 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(20): Show |
45 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.5117+1350T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305213 | |||||||
chr13:42305285 | T | C | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5117+1422T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305285 | |||||||
chr13:42305358 | T | A | 5 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.5117+1495T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305358 | |||||||
chr13:42305400 | A | G | 33 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0036 others(30): Show |
58 | HG00140.hp1 HG00733.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.5117+1537A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305400 | |||||||
chr13:42305437 | A | G | 1 | a0001c0010t0027g0046 | 2 | NA18969.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.5117+1574A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305437 | |||||||
chr13:42305441 | G | T | 29 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(26): Show |
60 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.5117+1578G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305441 | |||||||
chr13:42305446 | C | G | 2 | a0001c0001t0005g0073 a0001c0001t0005g0074 |
2 | HG01074.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.5117+1583C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305446 | |||||||
chr13:42305566 | G | A | 8 | a0001c0001t0020g0176 a0001c0003t0010g0017 a0001c0003t0010g0043 others(5): Show |
10 | HG00099.hp1 HG00544.hp1 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.5117+1703G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305566 | |||||||
chr13:42305668 | T | C | 5 | a0001c0001t0012g0007 a0001c0001t0012g0119 a0008c0011t0011g0117 others(2): Show |
10 | HG00140.hp1 HG00733.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.5117+1805T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305668 | |||||||
chr13:42305868 | A | T | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5117+2005A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305868 | |||||||
chr13:42305902 | G | A | 5 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.5117+2039G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305902 | |||||||
chr13:42305919 | G | A | 23 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(20): Show |
45 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.5117+2056G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42305919 | |||||||
chr13:42306006 | C | T | 1 | a0016c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5117+2143C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42306006 | |||||||
chr13:42306622 | G | A | 1 | a0001c0001t0009g0079 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5118-1832G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42306622 | |||||||
chr13:42306710 | A | G | 1 | a0001c0001t0012g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5118-1744A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42306710 | |||||||
chr13:42306833 | A | G | 15 | a0001c0001t0003g0196 a0001c0001t0021g0005 a0001c0001t0021g0030 others(12): Show |
21 | HG00438.hp2 HG00609.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.5118-1621A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42306833 | |||||||
chr13:42306994 | A | G | 1 | a0001c0001t0009g0087 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.5118-1460A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42306994 | |||||||
chr13:42307011 | C | T | 1 | a0001c0001t0005g0086 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.5118-1443C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307011 | |||||||
chr13:42307151 | A | G | 1 | a0014c0030t0083g0194 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5118-1303A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307151 | |||||||
chr13:42307173 | T | A | 5 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(2): Show |
14 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.5118-1281T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307173 | |||||||
chr13:42307231 | T | C | 11 | a0002c0004t0007g0123 a0002c0004t0007g0124 a0002c0004t0007g0127 others(8): Show |
17 | HG00408.hp1 HG00423.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.5118-1223T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307231 | |||||||
chr13:42307584 | C | T | 1 | a0001c0001t0085g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5118-870C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307584 | |||||||
chr13:42307665 | G | T | 116 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(113): Show |
153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.5118-789G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307665 | |||||||
chr13:42307666 | A | T | 116 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(113): Show |
153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.5118-788A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307666 | |||||||
chr13:42307772 | C | T | 1 | a0001c0001t0005g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5118-682C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307772 | |||||||
chr13:42307791 | T | TGGAA | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5118-660_5118-657d others(6): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 42307791 | ||||||
chr13:42307806 | C | A | 256 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0036 others(253): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.5118-648C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42307806 | |||||||
chr13:42308032 | T | C | 1 | a0004c0009t0073g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5118-422T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42308032 | |||||||
chr13:42308251 | G | A | 1 | a0011c0012t0034g0035 | 2 | HG01981.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.5118-203G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 8/12 | chr13 | 42308251 | |||||||
chr13:42308626 | A | G | 211 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(208): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.5273+17A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42308626 | |||||||
chr13:42308902 | A | AT | 116 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(113): Show |
153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.5273+303dupT | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 42308902 | ||||||
chr13:42308902 | A | T | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5273+293A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42308902 | |||||||
chr13:42308951 | G | A | 1 | a0001c0001t0006g0101 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.5273+342G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42308951 | |||||||
chr13:42308976 | G | C | 1 | a0001c0002t0017g0018 | 3 | NA18957.hp2 NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.5273+367G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42308976 | |||||||
chr13:42309004 | A | G | 1 | a0014c0030t0083g0194 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5273+395A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309004 | |||||||
chr13:42309009 | A | G | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.5273+400A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309009 | |||||||
chr13:42309037 | G | A | 1 | a0001c0019t0081g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5273+428G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309037 | |||||||
chr13:42309144 | T | A | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.5273+535T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309144 | |||||||
chr13:42309149 | C | CA | 23 | a0001c0003t0010g0017 a0001c0003t0010g0023 a0001c0003t0010g0042 others(20): Show |
30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.5273+542dupA | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 42309149 | ||||||
chr13:42309256 | T | G | 1 | a0001c0001t0016g0163 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5273+647T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309256 | |||||||
chr13:42309318 | G | A | 1 | a0001c0001t0028g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5273+709G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309318 | |||||||
chr13:42309353 | G | A | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5273+744G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309353 | |||||||
chr13:42309630 | A | G | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5273+1021A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309630 | |||||||
chr13:42309674 | G | A | 147 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(144): Show |
194 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.5273+1065G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42309674 | |||||||
chr13:42310322 | G | T | 1 | a0001c0001t0005g0074 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.5273+1713G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310322 | |||||||
chr13:42310333 | A | G | 1 | a0001c0003t0010g0042 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.5273+1724A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310333 | |||||||
chr13:42310425 | A | G | 3 | a0001c0001t0055g0190 a0001c0001t0057g0191 a0001c0001t0058g0189 |
3 | HG02809.hp2 HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5273+1816A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310425 | |||||||
chr13:42310501 | A | G | 2 | a0001c0002t0001g0027 a0001c0026t0001g0027 |
2 | NA18945.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.5273+1892A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310501 | |||||||
chr13:42310579 | G | A | 1 | a0001c0002t0001g0028 | 2 | HG00597.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.5273+1970G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310579 | |||||||
chr13:42310590 | C | T | 3 | a0004c0009t0072g0173 a0004c0009t0073g0175 a0004c0009t0080g0174 |
3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5273+1981C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310590 | |||||||
chr13:42310624 | G | A | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5273+2015G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42310624 | |||||||
chr13:42310856 | CA | C | 124 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(121): Show |
161 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.5274-2175delA | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 42310856 | ||||||
chr13:42311006 | A | G | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5274-2041A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311006 | |||||||
chr13:42311017 | CTCTG | C | 119 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(116): Show |
156 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.5274-2024_5274-202 others(8): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 42311017 | ||||||
chr13:42311132 | A | G | 30 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(27): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.5274-1915A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311132 | |||||||
chr13:42311425 | A | G | 2 | a0009c0014t0022g0151 a0009c0014t0022g0152 |
2 | HG01123.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.5274-1622A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311425 | |||||||
chr13:42311541 | G | A | 1 | a0001c0001t0013g0182 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5274-1506G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311541 | |||||||
chr13:42311835 | A | G | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5274-1212A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311835 | |||||||
chr13:42311916 | A | G | 1 | a0001c0003t0025g0156 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5274-1131A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42311916 | |||||||
chr13:42312029 | A | C | 1 | a0001c0001t0009g0079 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5274-1018A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312029 | |||||||
chr13:42312099 | T | C | 1 | a0001c0001t0005g0081 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.5274-948T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312099 | |||||||
chr13:42312114 | T | C | 1 | a0001c0001t0009g0068 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5274-933T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312114 | |||||||
chr13:42312311 | G | A | 2 | a0010c0015t0013g0181 a0010c0015t0028g0179 |
2 | HG01256.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5274-736G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312311 | |||||||
chr13:42312595 | A | G | 4 | a0001c0003t0025g0024 a0001c0003t0025g0145 a0001c0003t0025g0155 others(1): Show |
6 | HG02109.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.5274-452A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312595 | |||||||
chr13:42312732 | A | G | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.5274-315A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312732 | |||||||
chr13:42312832 | C | T | 3 | a0001c0001t0006g0020 a0001c0001t0014g0020 a0001c0001t0070g0020 |
3 | NA18961.hp2 NA18984.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.5274-215C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312832 | |||||||
chr13:42312875 | A | G | 1 | a0001c0001t0006g0085 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5274-172A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312875 | |||||||
chr13:42312905 | A | G | 1 | a0016c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5274-142A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312905 | |||||||
chr13:42312909 | C | T | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5274-138C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312909 | |||||||
chr13:42312991 | G | T | 1 | a0001c0001t0085g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5274-56G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42312991 | |||||||
chr13:42313001 | A | G | 6 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(3): Show |
10 | HG01975.hp2 HG02257.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.5274-46A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 9/12 | chr13 | 42313001 | |||||||
chr13:42313277 | C | A | 1 | a0014c0030t0083g0194 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5357+147C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 10/12 | chr13 | 42313277 | |||||||
chr13:42313385 | A | T | 1 | a0001c0001t0062g0100 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5357+255A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 10/12 | chr13 | 42313385 | |||||||
chr13:42313430 | G | C | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5357+300G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 10/12 | chr13 | 42313430 | |||||||
chr13:42313519 | A | T | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.5358-375A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 10/12 | chr13 | 42313519 | |||||||
chr13:42313820 | T | C | 1 | a0001c0001t0002g0039 | 2 | HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.5358-74T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 10/12 | chr13 | 42313820 | |||||||
chr13:42313968 | G | T | 1 | a0001c0002t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5404+28G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42313968 | |||||||
chr13:42314094 | A | G | 146 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(143): Show |
193 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.5404+154A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314094 | |||||||
chr13:42314224 | C | T | 1 | a0016c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5404+284C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314224 | |||||||
chr13:42314274 | A | G | 1 | a0001c0003t0010g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5404+334A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314274 | |||||||
chr13:42314343 | G | A | 7 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(4): Show |
12 | HG01975.hp2 HG01981.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5404+403G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314343 | |||||||
chr13:42314394 | G | A | 3 | a0004c0009t0072g0173 a0004c0009t0073g0175 a0004c0009t0080g0174 |
3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5404+454G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314394 | |||||||
chr13:42314446 | TAAAA | T | 13 | a0001c0001t0015g0014 a0001c0001t0015g0110 a0001c0001t0015g0111 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.5404+527_5404+530d others(6): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 42314446 | ||||||
chr13:42314446 | TAAAAA | T | 9 | a0001c0001t0003g0076 a0001c0001t0003g0082 a0001c0001t0006g0103 others(6): Show |
12 | HG00639.hp1 HG00733.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.5404+526_5404+530d others(7): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 42314446 | ||||||
chr13:42314446 | TAAAAAA | T | 139 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(136): Show |
198 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.5404+525_5404+530d others(8): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 42314446 | ||||||
chr13:42314446 | TAAAAAAA | T | 23 | a0001c0003t0010g0017 a0001c0003t0010g0023 a0001c0003t0010g0042 others(20): Show |
30 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.5404+524_5404+530d others(9): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 42314446 | ||||||
chr13:42314447 | A | T | 1 | a0022c0024t0049g0131 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5404+507A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314447 | |||||||
chr13:42314798 | T | A | 1 | a0016c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5404+858T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314798 | |||||||
chr13:42314873 | T | C | 3 | a0001c0001t0006g0034 a0001c0001t0014g0105 a0021c0016t0065g0034 |
3 | NA18951.hp1 NA18986.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.5404+933T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314873 | |||||||
chr13:42314911 | G | C | 1 | a0001c0001t0085g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5404+971G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42314911 | |||||||
chr13:42315127 | A | T | 1 | a0016c0018t0076g0106 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5404+1187A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315127 | |||||||
chr13:42315186 | A | C | 119 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(116): Show |
156 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.5404+1246A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315186 | |||||||
chr13:42315496 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5404+1556C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315496 | |||||||
chr13:42315543 | TTAAC | T | 119 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(116): Show |
156 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.5404+1606_5404+160 others(8): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 42315543 | ||||||
chr13:42315622 | T | G | 4 | a0001c0001t0002g0040 a0001c0001t0002g0132 a0001c0001t0036g0040 others(1): Show |
4 | HG02647.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.5404+1682T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315622 | |||||||
chr13:42315639 | C | T | 1 | a0005c0007t0039g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5404+1699C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315639 | |||||||
chr13:42315642 | G | A | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5404+1702G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315642 | |||||||
chr13:42315938 | A | G | 1 | a0001c0001t0013g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5405-1590A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315938 | |||||||
chr13:42315962 | C | T | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.5405-1566C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315962 | |||||||
chr13:42315973 | G | T | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.5405-1555G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42315973 | |||||||
chr13:42316137 | G | A | 184 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(181): Show |
267 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.5405-1391G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316137 | |||||||
chr13:42316187 | T | G | 4 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(1): Show |
13 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.5405-1341T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316187 | |||||||
chr13:42316242 | C | T | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.5405-1286C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316242 | |||||||
chr13:42316284 | C | T | 1 | a0001c0001t0085g0138 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5405-1244C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316284 | |||||||
chr13:42316303 | T | G | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5405-1225T>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316303 | |||||||
chr13:42316308 | A | C | 1 | a0001c0019t0081g0172 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5405-1220A>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316308 | |||||||
chr13:42316427 | G | A | 1 | a0001c0001t0013g0182 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5405-1101G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316427 | |||||||
chr13:42316525 | G | A | 1 | a0001c0001t0003g0066 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.5405-1003G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316525 | |||||||
chr13:42316563 | G | A | 6 | a0003c0005t0008g0006 a0003c0005t0075g0063 a0003c0022t0008g0199 others(3): Show |
15 | HG00423.hp2 HG00609.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.5405-965G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316563 | |||||||
chr13:42316703 | C | T | 1 | a0001c0001t0020g0084 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.5405-825C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316703 | |||||||
chr13:42316908 | A | G | 37 | a0001c0001t0015g0014 a0001c0001t0015g0109 a0001c0001t0015g0110 others(34): Show |
73 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.5405-620A>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42316908 | |||||||
chr13:42317005 | G | A | 3 | a0001c0001t0055g0190 a0001c0001t0057g0191 a0001c0001t0058g0189 |
3 | HG02809.hp2 HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5405-523G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317005 | |||||||
chr13:42317013 | G | C | 1 | a0001c0001t0031g0016 | 4 | HG02109.hp2 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5405-515G>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317013 | |||||||
chr13:42317034 | C | T | 30 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(27): Show |
61 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.5405-494C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317034 | |||||||
chr13:42317127 | G | A | 1 | a0017c0017t0041g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5405-401G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317127 | |||||||
chr13:42317130 | G | A | 3 | a0005c0007t0034g0142 a0005c0007t0039g0140 a0005c0007t0039g0141 |
3 | HG03098.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.5405-398G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317130 | |||||||
chr13:42317260 | G | A | 24 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0027 others(21): Show |
46 | HG00597.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.5405-268G>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317260 | |||||||
chr13:42317371 | T | C | 1 | a0001c0001t0055g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5405-157T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317371 | |||||||
chr13:42317452 | G | T | 3 | a0001c0001t0020g0021 a0001c0001t0067g0021 a0001c0001t0069g0021 |
3 | HG03486.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5405-76G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 11/12 | chr13 | 42317452 | |||||||
chr13:42317749 | GTGATTGG others(10): Show |
G | 1 | a0001c0001t0035g0164 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5565+64_5565+80del others(17): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 42317749 | ||||||
chr13:42317777 | T | A | 1 | a0001c0001t0021g0089 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.5565+89T>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42317777 | |||||||
chr13:42317804 | A | T | 3 | a0001c0003t0093g0157 a0001c0003t0094g0153 a0015c0020t0095g0154 |
3 | HG03139.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5565+116A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42317804 | |||||||
chr13:42317919 | C | T | 1 | a0001c0003t0025g0145 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5565+231C>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42317919 | |||||||
chr13:42318339 | A | T | 7 | a0001c0001t0003g0010 a0001c0001t0003g0019 a0001c0001t0006g0010 others(4): Show |
10 | HG01928.hp2 HG03834.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.5565+651A>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42318339 | |||||||
chr13:42318459 | C | G | 1 | a0010c0015t0028g0179 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5566-629C>G | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42318459 | |||||||
chr13:42318557 | G | GTATT | 8 | a0001c0001t0016g0158 a0001c0001t0016g0160 a0001c0001t0016g0161 others(5): Show |
10 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.5566-513_5566-510d others(6): Show |
AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 42318557 | ||||||
chr13:42318633 | T | C | 1 | a0001c0001t0005g0083 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.5566-455T>C | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42318633 | |||||||
chr13:42318667 | C | A | 1 | a0004c0009t0080g0174 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5566-421C>A | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42318667 | |||||||
chr13:42318770 | G | T | 1 | a0001c0002t0001g0056 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.5566-318G>T | AKAP11 | ENSG00000023516.9 | transcript | ENST00000025301.4 | protein_coding | 12/12 | chr13 | 42318770 |