Item | Value |
---|---|
geneid | 85459 |
ensemblid | ENSG00000166004.15 |
hgncid | 29366 |
symbol | CEP295 |
name | centrosomal protein 295 |
refseq_nuc | NM_033395.2 |
refseq_prot | NP_203753.1 |
ensembl_nuc | ENST00000325212.11 |
ensembl_prot | ENSP00000316681.6 |
mane_status | MANE Select |
chr | chr11 |
start | 93661682 |
end | 93730358 |
strand | + |
ver | v1.2 |
region | chr11:93661682-93730358 |
region5000 | chr11:93656682-93735358 |
regionname0 | CEP295_chr11_93661682_93730358 |
regionname5000 | CEP295_chr11_93656682_93735358 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2601 | 194 | 23 | 33 | 100 | 11 | 26 | 82 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0002 | 1/0 | 2601 | 39 | 27 | 6 | 4 | 0 | 1 | 4 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0003 | 0/0 | 2601 | 39 | 0 | 2 | 36 | 0 | 1 | 26 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0004 | 0/0 | 2601 | 17 | 7 | 6 | 0 | 3 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0005 | 0/0 | 2601 | 15 | 12 | 2 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0006 | 0/0 | 2601 | 13 | 0 | 0 | 13 | 0 | 0 | 12 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0007 | 0/0 | 2601 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0008 | 0/0 | 2601 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0009 | 0/0 | 2601 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0010 | 0/0 | 2601 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0011 | 0/0 | 2601 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0012 | 0/0 | 2601 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0013 | 0/0 | 2601 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0014 | 0/0 | 2601 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0015 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0016 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0017 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0018 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0019 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0020 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0021 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0022 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0023 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0024 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0025 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0026 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0027 | 0/0 | 2409 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2404): Show |
chr11 | 93656682 | 93735358 |
a0028 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0029 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0030 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0031 | 0/0 | 192 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(187): Show |
chr11 | 93656682 | 93735358 |
a0032 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
a0033 | 0/0 | 2601 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | MKRKV others(2596): Show |
chr11 | 93656682 | 93735358 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 7803 | 187 | 23 | 33 | 98 | 9 | 24 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0001c0012 | 0/1 | 7803 | 2 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0001c0013 | 0/0 | 7803 | 2 | 0 | 0 | 0 | 0 | 2 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0001c0016 | 0/0 | 7803 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0001c0032 | 0/0 | 7803 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0002c0003 | 1/0 | 7803 | 34 | 22 | 6 | 4 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0002c0010 | 0/0 | 7803 | 3 | 3 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0002c0019 | 0/0 | 7803 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0003c0002 | 0/0 | 7803 | 39 | 0 | 2 | 36 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0004c0005 | 0/0 | 7803 | 12 | 2 | 6 | 0 | 3 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0004c0009 | 0/0 | 7803 | 3 | 3 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0004c0043 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0004c0047 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0005c0006 | 0/0 | 7803 | 9 | 8 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0005c0011 | 0/0 | 7803 | 2 | 1 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0005c0014 | 0/0 | 7803 | 2 | 1 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0005c0026 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0005c0033 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0006c0004 | 0/0 | 7803 | 12 | 0 | 0 | 12 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0006c0037 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0007c0007 | 0/0 | 7803 | 4 | 4 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0008c0008 | 0/0 | 7803 | 4 | 4 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0009c0017 | 0/0 | 7803 | 2 | 1 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0010c0020 | 0/0 | 7803 | 2 | 0 | 0 | 1 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0011c0018 | 0/0 | 7803 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0012c0015 | 0/0 | 7803 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0013c0034 | 0/0 | 7803 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0014c0023 | 0/0 | 7803 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0015c0024 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0016c0028 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0017c0041 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0018c0038 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0019c0035 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0020c0021 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0021c0040 | 0/0 | 7803 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0022c0025 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0023c0022 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0024c0036 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0025c0045 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0026c0030 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0027c0039 | 0/0 | 7847 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7842): Show |
chr11 | 93656682 | 93735358 | ||
a0028c0027 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0029c0029 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0030c0031 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0031c0044 | 0/0 | 7781 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7776): Show |
chr11 | 93656682 | 93735358 | ||
a0032c0046 | 0/0 | 7803 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 | ||
a0033c0042 | 0/0 | 7803 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | ATGAA others(7798): Show |
chr11 | 93656682 | 93735358 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8014 | 187 | 23 | 33 | 98 | 9 | 24 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0001c0012t0001 | 0/1 | 8014 | 2 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0001c0013t0001 | 0/0 | 8014 | 2 | 0 | 0 | 0 | 0 | 2 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0001c0016t0001 | 0/0 | 8014 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0001c0032t0001 | 0/0 | 8014 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0002c0003t0001 | 1/0 | 8014 | 34 | 22 | 6 | 4 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0002c0010t0001 | 0/0 | 8014 | 3 | 3 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0002c0019t0001 | 0/0 | 8014 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0003c0002t0001 | 0/0 | 8014 | 39 | 0 | 2 | 36 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0004c0005t0001 | 0/0 | 8014 | 11 | 1 | 6 | 0 | 3 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0004c0005t0003 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0004c0009t0001 | 0/0 | 8014 | 3 | 3 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0004c0043t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0004c0047t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0005c0006t0001 | 0/0 | 8014 | 9 | 8 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0005c0011t0001 | 0/0 | 8014 | 2 | 1 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0005c0014t0001 | 0/0 | 8014 | 2 | 1 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0005c0026t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0005c0033t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0006c0004t0001 | 0/0 | 8014 | 12 | 0 | 0 | 12 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0006c0037t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0007c0007t0001 | 0/0 | 8014 | 4 | 4 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0008c0008t0001 | 0/0 | 8014 | 4 | 4 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0009c0017t0002 | 0/0 | 8014 | 2 | 1 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0010c0020t0001 | 0/0 | 8014 | 2 | 0 | 0 | 1 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0011c0018t0001 | 0/0 | 8014 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0012c0015t0001 | 0/0 | 8014 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0013c0034t0001 | 0/0 | 8014 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0014c0023t0001 | 0/0 | 8014 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0015c0024t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0016c0028t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0017c0041t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0018c0038t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0019c0035t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0020c0021t0001 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0021c0040t0004 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0022c0025t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0023c0022t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0024c0036t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0025c0045t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0026c0030t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0027c0039t0001 | 0/0 | 8058 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8053): Show |
chr11 | 93656682 | 93735358 |
a0028c0027t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0029c0029t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0030c0031t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0031c0044t0001 | 0/0 | 7992 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(7987): Show |
chr11 | 93656682 | 93735358 |
a0032c0046t0001 | 0/0 | 8014 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
a0033c0042t0001 | 0/0 | 8014 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | GCAGA others(8009): Show |
chr11 | 93656682 | 93735358 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0008 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0012t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0012t0001g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0013t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0013t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0016t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0001c0032t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0300 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0010t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0010t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0019t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0002c0019t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0003c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0005t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0009t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0009t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0009t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0043t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0004c0047t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0006t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0011t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0011t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0014t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0014t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0026t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0005c0033t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0006c0037t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0007c0007t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0007c0007t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0007c0007t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0007c0007t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0008c0008t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0008c0008t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0008c0008t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0009c0017t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0009c0017t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0010c0020t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0010c0020t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0011c0018t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0011c0018t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0012c0015t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0012c0015t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0013c0034t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0014c0023t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0015c0024t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0016c0028t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0017c0041t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0018c0038t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0019c0035t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0020c0021t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0021c0040t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0022c0025t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0023c0022t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0024c0036t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0025c0045t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0026c0030t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0027c0039t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0028c0027t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0029c0029t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0030c0031t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0031c0044t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0032c0046t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
a0033c0042t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0005 | t0001 | g0100 | EUR | GBR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00140 | hp1 | a0004 | c0005 | t0001 | g0098 | EUR | GBR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | GBR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00408 | hp1 | a0003 | c0002 | t0001 | g0079 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00558 | hp2 | a0003 | c0002 | t0001 | g0103 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00609 | hp2 | a0003 | c0002 | t0001 | g0087 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00621 | hp2 | a0003 | c0002 | t0001 | g0001 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00673 | hp1 | a0003 | c0002 | t0001 | g0106 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG00741 | hp2 | a0005 | c0006 | t0001 | g0043 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01074 | hp2 | a0002 | c0003 | t0001 | g0292 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01081 | hp1 | a0002 | c0003 | t0001 | g0285 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01099 | hp1 | a0009 | c0017 | t0002 | g0307 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01106 | hp2 | a0004 | c0005 | t0001 | g0101 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01109 | hp1 | a0013 | c0034 | t0001 | g0059 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01167 | hp2 | a0003 | c0002 | t0001 | g0120 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01168 | hp1 | a0004 | c0005 | t0001 | g0088 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01169 | hp1 | a0004 | c0005 | t0001 | g0097 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01192 | hp1 | a0002 | c0003 | t0001 | g0278 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01243 | hp1 | a0002 | c0003 | t0001 | g0274 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01243 | hp2 | a0002 | c0003 | t0001 | g0298 | AMR | PUR | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01255 | hp1 | a0014 | c0023 | t0001 | g0243 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01255 | hp2 | a0004 | c0005 | t0001 | g0111 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01261 | hp2 | a0004 | c0005 | t0001 | g0247 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01361 | hp1 | a0004 | c0005 | t0001 | g0113 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01361 | hp2 | a0002 | c0003 | t0001 | g0276 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01515 | hp1 | a0001 | c0032 | t0001 | g0250 | EUR | IBS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01884 | hp2 | a0002 | c0010 | t0001 | g0022 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01891 | hp1 | a0002 | c0003 | t0001 | g0287 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01891 | hp2 | a0005 | c0011 | t0001 | g0242 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02004 | hp1 | a0005 | c0014 | t0001 | g0076 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02015 | hp2 | a0003 | c0002 | t0001 | g0092 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02055 | hp1 | a0004 | c0043 | t0001 | g0122 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02055 | hp2 | a0005 | c0006 | t0001 | g0061 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02056 | hp1 | a0015 | c0024 | t0001 | g0168 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02071 | hp1 | a0003 | c0002 | t0001 | g0104 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02129 | hp2 | a0003 | c0002 | t0001 | g0089 | EAS | KHV | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02145 | hp2 | a0007 | c0007 | t0001 | g0072 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02148 | hp2 | a0003 | c0002 | t0001 | g0118 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02165 | hp1 | a0006 | c0004 | t0001 | g0002 | EAS | CDX | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CDX | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02257 | hp1 | a0005 | c0006 | t0001 | g0039 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02258 | hp1 | a0002 | c0003 | t0001 | g0297 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02258 | hp2 | a0002 | c0003 | t0001 | g0290 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02280 | hp2 | a0005 | c0014 | t0001 | g0077 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02451 | hp1 | a0008 | c0008 | t0001 | g0010 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02451 | hp2 | a0002 | c0003 | t0001 | g0023 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02572 | hp1 | a0005 | c0006 | t0001 | g0041 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02572 | hp2 | a0002 | c0010 | t0001 | g0286 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02615 | hp1 | a0002 | c0003 | t0001 | g0275 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02615 | hp2 | a0004 | c0047 | t0001 | g0249 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02630 | hp1 | a0002 | c0003 | t0001 | g0279 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02630 | hp2 | a0002 | c0003 | t0001 | g0289 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0293 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02683 | hp1 | a0010 | c0020 | t0001 | g0099 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02698 | hp1 | a0002 | c0003 | t0001 | g0280 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02723 | hp1 | a0017 | c0041 | t0001 | g0284 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02723 | hp2 | a0002 | c0003 | t0001 | g0296 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02809 | hp1 | a0011 | c0018 | t0001 | g0306 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0024 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02818 | hp2 | a0018 | c0038 | t0001 | g0273 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02886 | hp1 | a0005 | c0006 | t0001 | g0035 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02886 | hp2 | a0011 | c0018 | t0001 | g0305 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02895 | hp2 | a0005 | c0006 | t0001 | g0268 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02896 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02897 | hp2 | a0005 | c0006 | t0001 | g0269 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02922 | hp1 | a0002 | c0003 | t0001 | g0295 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02965 | hp2 | a0008 | c0008 | t0001 | g0119 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02976 | hp1 | a0004 | c0005 | t0001 | g0083 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03041 | hp1 | a0002 | c0003 | t0001 | g0020 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03041 | hp2 | a0005 | c0033 | t0001 | g0038 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03098 | hp1 | a0002 | c0003 | t0001 | g0288 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03098 | hp2 | a0005 | c0026 | t0001 | g0044 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03130 | hp1 | a0008 | c0008 | t0001 | g0010 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03130 | hp2 | a0004 | c0009 | t0001 | g0121 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03139 | hp1 | a0002 | c0003 | t0001 | g0021 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03139 | hp2 | a0019 | c0035 | t0001 | g0060 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03195 | hp2 | a0002 | c0010 | t0001 | g0022 | AFR | ESN | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03209 | hp1 | a0020 | c0021 | t0001 | g0073 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03209 | hp2 | a0002 | c0003 | t0001 | g0020 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03453 | hp2 | a0002 | c0003 | t0001 | g0277 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03486 | hp1 | a0007 | c0007 | t0001 | g0071 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03486 | hp2 | a0002 | c0003 | t0001 | g0023 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03540 | hp1 | a0007 | c0007 | t0001 | g0075 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03540 | hp2 | a0004 | c0005 | t0003 | g0026 | AFR | GWD | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03579 | hp1 | a0009 | c0017 | t0002 | g0304 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03579 | hp2 | a0021 | c0040 | t0004 | g0294 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03688 | hp1 | a0004 | c0005 | t0001 | g0011 | SAS | STU | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03831 | hp1 | a0003 | c0002 | t0001 | g0116 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03834 | hp2 | a0001 | c0013 | t0001 | g0202 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03942 | hp1 | a0001 | c0013 | t0001 | g0205 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18522 | hp1 | a0005 | c0006 | t0001 | g0042 | AFR | YRI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18522 | hp2 | a0004 | c0009 | t0001 | g0037 | AFR | YRI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18612 | hp2 | a0003 | c0002 | t0001 | g0091 | EAS | CHB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18747 | hp1 | a0003 | c0002 | t0001 | g0006 | EAS | CHB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18940 | hp1 | a0003 | c0002 | t0001 | g0107 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18940 | hp2 | a0006 | c0004 | t0001 | g0033 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18941 | hp1 | a0006 | c0004 | t0001 | g0002 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18942 | hp2 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18945 | hp1 | a0003 | c0002 | t0001 | g0006 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18948 | hp2 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18949 | hp1 | a0003 | c0002 | t0001 | g0109 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18949 | hp2 | a0022 | c0025 | t0001 | g0003 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18951 | hp2 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18953 | hp1 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18954 | hp2 | a0003 | c0002 | t0001 | g0006 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18956 | hp2 | a0023 | c0022 | t0001 | g0246 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18964 | hp1 | a0003 | c0002 | t0001 | g0095 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18966 | hp1 | a0003 | c0002 | t0001 | g0085 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18968 | hp2 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18969 | hp1 | a0006 | c0004 | t0001 | g0027 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18971 | hp2 | a0006 | c0004 | t0001 | g0002 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18973 | hp2 | a0003 | c0002 | t0001 | g0110 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18975 | hp2 | a0024 | c0036 | t0001 | g0002 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18979 | hp1 | a0003 | c0002 | t0001 | g0094 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18980 | hp1 | a0025 | c0045 | t0001 | g0011 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18982 | hp1 | a0006 | c0004 | t0001 | g0031 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18984 | hp2 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18985 | hp1 | a0026 | c0030 | t0001 | g0211 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18986 | hp2 | a0027 | c0039 | t0001 | g0301 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18988 | hp2 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18991 | hp1 | a0003 | c0002 | t0001 | g0105 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18994 | hp2 | a0003 | c0002 | t0001 | g0078 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18997 | hp2 | a0006 | c0004 | t0001 | g0029 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19000 | hp1 | a0003 | c0002 | t0001 | g0102 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19000 | hp2 | a0003 | c0002 | t0001 | g0081 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19002 | hp1 | a0002 | c0003 | t0001 | g0302 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19002 | hp2 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19007 | hp1 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19009 | hp2 | a0006 | c0004 | t0001 | g0002 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19011 | hp2 | a0003 | c0002 | t0001 | g0115 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19030 | hp1 | a0002 | c0003 | t0001 | g0281 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19030 | hp2 | a0002 | c0019 | t0001 | g0283 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19043 | hp2 | a0002 | c0003 | t0001 | g0299 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19054 | hp1 | a0028 | c0027 | t0001 | g0128 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19054 | hp2 | a0002 | c0003 | t0001 | g0303 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19055 | hp1 | a0029 | c0029 | t0001 | g0142 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19058 | hp2 | a0012 | c0015 | t0001 | g0016 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19060 | hp1 | a0030 | c0031 | t0001 | g0224 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19060 | hp2 | a0006 | c0037 | t0001 | g0028 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19062 | hp2 | a0006 | c0004 | t0001 | g0002 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19063 | hp2 | a0003 | c0002 | t0001 | g0108 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19065 | hp1 | a0003 | c0002 | t0001 | g0093 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19067 | hp1 | a0003 | c0002 | t0001 | g0117 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19068 | hp2 | a0006 | c0004 | t0001 | g0034 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19070 | hp1 | a0003 | c0002 | t0001 | g0090 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19074 | hp1 | a0010 | c0020 | t0001 | g0084 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19076 | hp1 | a0031 | c0044 | t0001 | g0080 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19077 | hp1 | a0012 | c0015 | t0001 | g0198 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19077 | hp2 | a0001 | c0016 | t0001 | g0012 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19079 | hp1 | a0006 | c0004 | t0001 | g0032 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19080 | hp2 | a0001 | c0016 | t0001 | g0012 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19085 | hp1 | a0003 | c0002 | t0001 | g0086 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19086 | hp1 | a0006 | c0004 | t0001 | g0030 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19089 | hp1 | a0032 | c0046 | t0001 | g0114 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19090 | hp1 | a0003 | c0002 | t0001 | g0112 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA19240 | hp2 | a0007 | c0007 | t0001 | g0074 | AFR | YRI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20752 | hp1 | a0004 | c0005 | t0001 | g0096 | EUR | TSI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20805 | hp2 | a0001 | c0012 | t0001 | g0180 | EUR | TSI | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20905 | hp1 | a0005 | c0011 | t0001 | g0244 | SAS | GIH | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20905 | hp2 | a0033 | c0042 | t0001 | g0151 | SAS | GIH | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02109 | hp2 | a0016 | c0028 | t0001 | g0040 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02486 | hp2 | a0002 | c0003 | t0001 | g0021 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03471 | hp1 | a0008 | c0008 | t0001 | g0082 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
HG03471 | hp2 | a0002 | c0003 | t0001 | g0291 | AFR | MSL | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20300 | hp1 | a0004 | c0009 | t0001 | g0036 | AFR | USA | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA20300 | hp2 | a0005 | c0006 | t0001 | g0270 | AFR | USA | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA21309 | hp1 | a0002 | c0019 | t0001 | g0282 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
homoSapiens | chm13v2 | a0001 | c0012 | t0001 | g0218 | REF | REF | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
homoSapiens | grch38p0 | a0002 | c0003 | t0001 | g0300 | REF | REF | CEP295_chr11_93656682_93735358 | CEP295 | chr11 | 93656682 | 93735358 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:93667707 | A | G | 1 | a0033 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.209A>G | p.Glu70Gly | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/30 | 328/8014 | 209/7806 | 70/2601 | chr11 | 93667707 | |||
chr11:93667736 | C | A | 2 | a0007 a0020 |
5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
missense_variant | MODERATE | c.238C>A | p.Gln80Lys | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/30 | 357/8014 | 238/7806 | 80/2601 | chr11 | 93667736 | |||
chr11:93668910 | A | G | 1 | a0017 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.412A>G | p.Ile138Val | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/30 | 531/8014 | 412/7806 | 138/2601 | chr11 | 93668910 | |||
chr11:93675578 | AAGTAAAA others(15): Show |
A | 1 | a0031 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.538_559delGTAAAAAG others(14): Show |
p.Val180fs | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/30 | 657/8014 | 538/7806 | 180/2601 | INFO_REALIGN_3_PRIME | chr11 | 93675578 | ||
chr11:93675665 | G | A | 28 | a0001 a0003 a0004 others(25): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
missense_variant&splice_region_variant | MODERATE | c.623G>A | p.Arg208Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/30 | 742/8014 | 623/7806 | 208/2601 | chr11 | 93675665 | |||
chr11:93679421 | C | T | 2 | a0013 a0019 |
2 | HG01109.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.634C>T | p.Arg212Cys | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/30 | 753/8014 | 634/7806 | 212/2601 | chr11 | 93679421 | |||
chr11:93684086 | C | A | 1 | a0009 | 2 | HG01099.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.1072C>A | p.Leu358Ile | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/30 | 1191/8014 | 1072/7806 | 358/2601 | chr11 | 93684086 | |||
chr11:93687848 | C | T | 2 | a0009 a0011 |
4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
missense_variant | MODERATE | c.1319C>T | p.Ser440Phe | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/30 | 1438/8014 | 1319/7806 | 440/2601 | chr11 | 93687848 | |||
chr11:93691763 | G | A | 1 | a0018 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1417G>A | p.Gly473Arg | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 11/30 | 1536/8014 | 1417/7806 | 473/2601 | chr11 | 93691763 | |||
chr11:93691993 | C | A | 28 | a0001 a0003 a0004 others(25): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
missense_variant | MODERATE | c.1496C>A | p.Ala499Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/30 | 1615/8014 | 1496/7806 | 499/2601 | chr11 | 93691993 | |||
chr11:93695549 | T | C | 1 | a0023 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.1586T>C | p.Ile529Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 13/30 | 1705/8014 | 1586/7806 | 529/2601 | chr11 | 93695549 | |||
chr11:93696716 | C | G | 1 | a0010 | 2 | HG02683.hp1 NA19074.hp1 |
missense_variant | MODERATE | c.1804C>G | p.Gln602Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 1923/8014 | 1804/7806 | 602/2601 | chr11 | 93696716 | |||
chr11:93696992 | C | A | 1 | a0014 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.2080C>A | p.Arg694Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2199/8014 | 2080/7806 | 694/2601 | chr11 | 93696992 | |||
chr11:93697356 | G | C | 1 | a0020 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2444G>C | p.Ser815Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2563/8014 | 2444/7806 | 815/2601 | chr11 | 93697356 | |||
chr11:93697460 | C | T | 1 | a0008 | 4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
missense_variant | MODERATE | c.2548C>T | p.Leu850Phe | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2667/8014 | 2548/7806 | 850/2601 | chr11 | 93697460 | |||
chr11:93697503 | C | G | 4 | a0006 a0009 a0011 others(1): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
missense_variant | MODERATE | c.2591C>G | p.Thr864Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2710/8014 | 2591/7806 | 864/2601 | chr11 | 93697503 | |||
chr11:93697575 | T | C | 2 | a0009 a0011 |
4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
missense_variant | MODERATE | c.2663T>C | p.Phe888Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2782/8014 | 2663/7806 | 888/2601 | chr11 | 93697575 | |||
chr11:93697988 | G | A | 4 | a0006 a0009 a0011 others(1): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
missense_variant | MODERATE | c.3076G>A | p.Glu1026Lys | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3195/8014 | 3076/7806 | 1026/2601 | chr11 | 93697988 | |||
chr11:93698001 | T | C | 1 | a0015 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.3089T>C | p.Val1030Ala | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3208/8014 | 3089/7806 | 1030/2601 | chr11 | 93698001 | |||
chr11:93698471 | G | A | 1 | a0033 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.3559G>A | p.Val1187Ile | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3678/8014 | 3559/7806 | 1187/2601 | chr11 | 93698471 | |||
chr11:93698721 | C | G | 2 | a0006 a0024 |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
missense_variant | MODERATE | c.3809C>G | p.Ala1270Gly | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3928/8014 | 3809/7806 | 1270/2601 | chr11 | 93698721 | |||
chr11:93698765 | C | A | 6 | a0003 a0010 a0022 others(3): Show |
45 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(42): Show |
missense_variant | MODERATE | c.3853C>A | p.Gln1285Lys | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3972/8014 | 3853/7806 | 1285/2601 | chr11 | 93698765 | |||
chr11:93698931 | T | C | 1 | a0024 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.4019T>C | p.Ile1340Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4138/8014 | 4019/7806 | 1340/2601 | chr11 | 93698931 | |||
chr11:93699234 | G | A | 2 | a0006 a0024 |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
missense_variant | MODERATE | c.4322G>A | p.Gly1441Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4441/8014 | 4322/7806 | 1441/2601 | chr11 | 93699234 | |||
chr11:93699288 | T | G | 4 | a0006 a0009 a0011 others(1): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
missense_variant | MODERATE | c.4376T>G | p.Leu1459Arg | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4495/8014 | 4376/7806 | 1459/2601 | chr11 | 93699288 | |||
chr11:93699692 | A | C | 4 | a0006 a0009 a0011 others(1): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
missense_variant | MODERATE | c.4780A>C | p.Lys1594Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4899/8014 | 4780/7806 | 1594/2601 | chr11 | 93699692 | |||
chr11:93699714 | A | G | 1 | a0032 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.4802A>G | p.Asp1601Gly | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4921/8014 | 4802/7806 | 1601/2601 | chr11 | 93699714 | |||
chr11:93699797 | C | G | 1 | a0012 | 2 | NA19058.hp2 NA19077.hp1 |
missense_variant | MODERATE | c.4885C>G | p.Gln1629Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 5004/8014 | 4885/7806 | 1629/2601 | chr11 | 93699797 | |||
chr11:93699798 | A | G | 1 | a0021 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.4886A>G | p.Gln1629Arg | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 5005/8014 | 4886/7806 | 1629/2601 | chr11 | 93699798 | |||
chr11:93699858 | A | C | 2 | a0006 a0024 |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
missense_variant | MODERATE | c.4946A>C | p.Lys1649Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 5065/8014 | 4946/7806 | 1649/2601 | chr11 | 93699858 | |||
chr11:93706835 | C | T | 2 | a0026 a0030 |
2 | NA18985.hp1 NA19060.hp1 |
missense_variant | MODERATE | c.5687C>T | p.Pro1896Leu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/30 | 5806/8014 | 5687/7806 | 1896/2601 | chr11 | 93706835 | |||
chr11:93721377 | G | A | 2 | a0006 a0024 |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
missense_variant | MODERATE | c.5815G>A | p.Ala1939Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/30 | 5934/8014 | 5815/7806 | 1939/2601 | chr11 | 93721377 | |||
chr11:93724328 | T | C | 1 | a0025 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.6271T>C | p.Ser2091Pro | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/30 | 6390/8014 | 6271/7806 | 2091/2601 | chr11 | 93724328 | |||
chr11:93724359 | A | G | 1 | a0030 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.6302A>G | p.Asn2101Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/30 | 6421/8014 | 6302/7806 | 2101/2601 | chr11 | 93724359 | |||
chr11:93725777 | A | G | 2 | a0006 a0024 |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
missense_variant | MODERATE | c.6445A>G | p.Thr2149Ala | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/30 | 6564/8014 | 6445/7806 | 2149/2601 | chr11 | 93725777 | |||
chr11:93726994 | A | C | 7 | a0003 a0004 a0008 others(4): Show |
65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
missense_variant | MODERATE | c.6518A>C | p.Glu2173Ala | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 6637/8014 | 6518/7806 | 2173/2601 | chr11 | 93726994 | |||
chr11:93727098 | C | G | 1 | a0019 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.6622C>G | p.Gln2208Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 6741/8014 | 6622/7806 | 2208/2601 | chr11 | 93727098 | |||
chr11:93727477 | T | C | 1 | a0028 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.7001T>C | p.Ile2334Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 7120/8014 | 7001/7806 | 2334/2601 | chr11 | 93727477 | |||
chr11:93727480 | A | G | 1 | a0029 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.7004A>G | p.Gln2335Arg | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 7123/8014 | 7004/7806 | 2335/2601 | chr11 | 93727480 | |||
chr11:93728681 | G | GGGGGGGG others(37): Show |
1 | a0027 | 1 | NA18986.hp2 | frameshift_variant&splice_region_variant | HIGH | c.7162_7163insGGGGGG others(38): Show |
p.Glu2388fs | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/30 | 7282/8014 | 7163/7806 | 2388/2601 | chr11 | 93728681 | |||
chr11:93728702 | A | G | 1 | a0027 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.7183A>G | p.Ile2395Val | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/30 | 7302/8014 | 7183/7806 | 2395/2601 | chr11 | 93728702 | |||
chr11:93728729 | A | G | 3 | a0006 a0009 a0024 |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
missense_variant | MODERATE | c.7210A>G | p.Ile2404Val | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/30 | 7329/8014 | 7210/7806 | 2404/2601 | chr11 | 93728729 | |||
chr11:93729441 | A | T | 12 | a0001 a0012 a0013 others(9): Show |
205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
missense_variant | MODERATE | c.7310A>T | p.Glu2437Val | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 26/30 | 7429/8014 | 7310/7806 | 2437/2601 | chr11 | 93729441 | |||
chr11:93729474 | C | T | 1 | a0016 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.7343C>T | p.Ser2448Leu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 26/30 | 7462/8014 | 7343/7806 | 2448/2601 | chr11 | 93729474 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:93667630 | C | T | 9 | a0003c0002 a0004c0005 a0004c0043 others(6): Show |
62 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(59): Show |
synonymous_variant | LOW | c.132C>T | p.Ile44Ile | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/30 | 251/8014 | 132/7806 | 44/2601 | chr11 | 93667630 | |||
chr11:93668840 | A | G | 8 | a0003c0002 a0004c0005 a0004c0047 others(5): Show |
61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
synonymous_variant | LOW | c.342A>G | p.Ala114Ala | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/30 | 461/8014 | 342/7806 | 114/2601 | chr11 | 93668840 | |||
chr11:93668930 | C | A | 35 | a0001c0001 a0001c0012 a0001c0013 others(32): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
splice_region_variant&synonymous_variant | LOW | c.432C>A | p.Thr144Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/30 | 551/8014 | 432/7806 | 144/2601 | chr11 | 93668930 | |||
chr11:93696865 | C | G | 1 | a0005c0033 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1953C>G | p.Leu651Leu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2072/8014 | 1953/7806 | 651/2601 | chr11 | 93696865 | |||
chr11:93696943 | G | A | 1 | a0009c0017 | 2 | HG01099.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.2031G>A | p.Ala677Ala | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2150/8014 | 2031/7806 | 677/2601 | chr11 | 93696943 | |||
chr11:93697504 | T | A | 5 | a0006c0004 a0006c0037 a0009c0017 others(2): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
synonymous_variant | LOW | c.2592T>A | p.Thr864Thr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 2711/8014 | 2592/7806 | 864/2601 | chr11 | 93697504 | |||
chr11:93697876 | C | T | 5 | a0006c0004 a0006c0037 a0009c0017 others(2): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
synonymous_variant | LOW | c.2964C>T | p.Ser988Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3083/8014 | 2964/7806 | 988/2601 | chr11 | 93697876 | |||
chr11:93697996 | A | G | 1 | a0001c0032 | 1 | HG01515.hp1 | synonymous_variant | LOW | c.3084A>G | p.Gly1028Gly | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 3203/8014 | 3084/7806 | 1028/2601 | chr11 | 93697996 | |||
chr11:93698794 | G | A | 1 | a0004c0047 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.3882G>A | p.Gln1294Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4001/8014 | 3882/7806 | 1294/2601 | chr11 | 93698794 | |||
chr11:93698963 | T | C | 1 | a0002c0010 | 3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.4051T>C | p.Leu1351Leu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4170/8014 | 4051/7806 | 1351/2601 | chr11 | 93698963 | |||
chr11:93699199 | C | T | 1 | a0001c0016 | 2 | NA19077.hp2 NA19080.hp2 |
synonymous_variant | LOW | c.4287C>T | p.Ser1429Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4406/8014 | 4287/7806 | 1429/2601 | chr11 | 93699199 | |||
chr11:93699430 | G | A | 5 | a0006c0004 a0006c0037 a0009c0017 others(2): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
synonymous_variant | LOW | c.4518G>A | p.Gln1506Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4637/8014 | 4518/7806 | 1506/2601 | chr11 | 93699430 | |||
chr11:93699520 | A | G | 1 | a0002c0010 | 3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.4608A>G | p.Glu1536Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 4727/8014 | 4608/7806 | 1536/2601 | chr11 | 93699520 | |||
chr11:93699874 | G | T | 1 | a0006c0037 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.4962G>T | p.Ser1654Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 5081/8014 | 4962/7806 | 1654/2601 | chr11 | 93699874 | |||
chr11:93700096 | G | A | 5 | a0006c0004 a0006c0037 a0009c0017 others(2): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
synonymous_variant | LOW | c.5184G>A | p.Gln1728Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/30 | 5303/8014 | 5184/7806 | 1728/2601 | chr11 | 93700096 | |||
chr11:93702471 | C | T | 1 | a0005c0014 | 2 | HG02004.hp1 HG02280.hp2 |
synonymous_variant | LOW | c.5286C>T | p.Pro1762Pro | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 16/30 | 5405/8014 | 5286/7806 | 1762/2601 | chr11 | 93702471 | |||
chr11:93706776 | C | G | 1 | a0001c0013 | 2 | HG03834.hp2 HG03942.hp1 |
synonymous_variant | LOW | c.5628C>G | p.Pro1876Pro | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/30 | 5747/8014 | 5628/7806 | 1876/2601 | chr11 | 93706776 | |||
chr11:93721358 | T | C | 3 | a0001c0012 a0005c0011 a0014c0023 |
4 | HG01255.hp1 HG01891.hp2 NA20805.hp2 others(1): Show |
synonymous_variant | LOW | c.5796T>C | p.Tyr1932Tyr | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/30 | 5915/8014 | 5796/7806 | 1932/2601 | chr11 | 93721358 | |||
chr11:93725743 | T | G | 1 | a0005c0026 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.6411T>G | p.Ser2137Ser | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/30 | 6530/8014 | 6411/7806 | 2137/2601 | chr11 | 93725743 | |||
chr11:93727010 | A | G | 3 | a0006c0004 a0006c0037 a0024c0036 |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
synonymous_variant | LOW | c.6534A>G | p.Glu2178Glu | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 6653/8014 | 6534/7806 | 2178/2601 | chr11 | 93727010 | |||
chr11:93727481 | G | A | 1 | a0029c0029 | 1 | NA19055.hp1 | synonymous_variant | LOW | c.7005G>A | p.Gln2335Gln | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/30 | 7124/8014 | 7005/7806 | 2335/2601 | chr11 | 93727481 | |||
chr11:93728701 | T | G | 1 | a0027c0039 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.7182T>G | p.Gly2394Gly | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/30 | 7301/8014 | 7182/7806 | 2394/2601 | chr11 | 93728701 | |||
chr11:93729729 | T | C | 1 | a0002c0019 | 2 | NA19030.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.7515T>C | p.Ile2505Ile | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 27/30 | 7634/8014 | 7515/7806 | 2505/2601 | chr11 | 93729729 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:93661761 | C | A | 1 | a0004c0005t0003 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-40C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/30 | 4947 | chr11 | 93661761 | ||||||
chr11:93666690 | T | C | 1 | a0021c0040t0004 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-18T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/30 | 18 | chr11 | 93666690 | ||||||
chr11:93730330 | T | G | 1 | a0009c0017t0002 | 2 | HG01099.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*61T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 30/30 | 61 | chr11 | 93730330 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:93661890 | A | C | 4 | a0009c0017t0002g0304 a0009c0017t0002g0307 a0011c0018t0001g0305 others(1): Show |
4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+116A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93661890 | |||||||
chr11:93662020 | G | C | 1 | a0004c0005t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-27+246G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662020 | |||||||
chr11:93662155 | G | A | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.-27+381G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662155 | |||||||
chr11:93662307 | G | A | 1 | a0005c0006t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-27+533G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662307 | |||||||
chr11:93662356 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-27+582G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662356 | |||||||
chr11:93662650 | T | C | 2 | a0004c0009t0001g0036 a0004c0009t0001g0037 |
2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-27+876T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662650 | |||||||
chr11:93662748 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-27+974A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662748 | |||||||
chr11:93662883 | A | G | 4 | a0002c0003t0001g0025 a0002c0003t0001g0302 a0002c0003t0001g0303 others(1): Show |
5 | NA18953.hp1 NA18968.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27+1109A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93662883 | |||||||
chr11:93663011 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0271 |
3 | NA18966.hp2 NA18990.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-27+1237A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663011 | |||||||
chr11:93663043 | G | A | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-27+1269G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663043 | |||||||
chr11:93663267 | T | C | 1 | a0018c0038t0001g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-27+1493T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663267 | |||||||
chr11:93663296 | C | A | 3 | a0005c0006t0001g0039 a0005c0006t0001g0041 a0016c0028t0001g0040 |
3 | HG02109.hp2 HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-27+1522C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663296 | |||||||
chr11:93663521 | T | C | 2 | a0005c0006t0001g0042 a0005c0006t0001g0043 |
2 | HG00741.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-27+1747T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663521 | |||||||
chr11:93663660 | T | C | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-27+1886T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93663660 | |||||||
chr11:93664192 | CA | C | 6 | a0005c0006t0001g0039 a0005c0006t0001g0041 a0005c0006t0001g0268 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27+2419delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664192 | |||||||
chr11:93664334 | G | C | 18 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0025 others(15): Show |
21 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.-26-2348G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664334 | |||||||
chr11:93664373 | G | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0256 others(11): Show |
19 | HG00438.hp1 HG01081.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.-26-2309G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664373 | |||||||
chr11:93664415 | G | A | 1 | a0018c0038t0001g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-26-2267G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664415 | |||||||
chr11:93664451 | C | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-26-2231C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664451 | |||||||
chr11:93664473 | C | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26-2209C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664473 | |||||||
chr11:93664658 | C | T | 1 | a0001c0032t0001g0250 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-26-2024C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664658 | |||||||
chr11:93664676 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-26-2006C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664676 | |||||||
chr11:93664824 | C | T | 1 | a0004c0047t0001g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-26-1858C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664824 | |||||||
chr11:93664836 | G | A | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-26-1846G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93664836 | |||||||
chr11:93665131 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-26-1551A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665131 | |||||||
chr11:93665407 | C | A | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-1275C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665407 | |||||||
chr11:93665430 | G | A | 256 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(253): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-26-1252G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665430 | |||||||
chr11:93665477 | G | T | 1 | a0004c0005t0001g0247 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-26-1205G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665477 | |||||||
chr11:93665639 | C | T | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-26-1043C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665639 | |||||||
chr11:93665721 | A | G | 1 | a0009c0017t0002g0307 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-26-961A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665721 | |||||||
chr11:93665740 | C | T | 4 | a0009c0017t0002g0304 a0009c0017t0002g0307 a0011c0018t0001g0305 others(1): Show |
4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-942C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665740 | |||||||
chr11:93665944 | T | C | 20 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(17): Show |
20 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-26-738T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665944 | |||||||
chr11:93665994 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-26-688T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93665994 | |||||||
chr11:93666019 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-26-663G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666019 | |||||||
chr11:93666212 | C | T | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-26-470C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666212 | |||||||
chr11:93666214 | A | G | 1 | a0001c0032t0001g0250 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-26-468A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666214 | |||||||
chr11:93666232 | C | T | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-26-450C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666232 | |||||||
chr11:93666236 | G | A | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-446G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666236 | |||||||
chr11:93666401 | C | G | 1 | a0023c0022t0001g0246 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-26-281C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666401 | |||||||
chr11:93666519 | G | A | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26-163G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666519 | |||||||
chr11:93666599 | A | C | 1 | a0001c0001t0001g0245 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-26-83A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | chr11 | 93666599 | |||||||
chr11:93666650 | A | AT | 6 | a0005c0006t0001g0039 a0005c0006t0001g0041 a0005c0006t0001g0268 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26-27dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr11 | 93666650 | ||||||
chr11:93666832 | A | G | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.108+17A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93666832 | |||||||
chr11:93666837 | G | A | 3 | a0006c0004t0001g0027 a0006c0004t0001g0029 a0006c0037t0001g0028 |
3 | NA18969.hp1 NA18997.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.108+22G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93666837 | |||||||
chr11:93666886 | G | A | 293 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.108+71G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93666886 | |||||||
chr11:93666940 | A | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.108+125A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93666940 | |||||||
chr11:93667016 | T | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 |
3 | HG01256.hp1 HG02145.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.108+201T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93667016 | |||||||
chr11:93667054 | A | G | 1 | a0002c0010t0001g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.108+239A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93667054 | |||||||
chr11:93667111 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.108+296T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93667111 | |||||||
chr11:93667137 | T | C | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.108+322T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93667137 | |||||||
chr11:93667337 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.109-270G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 2/29 | chr11 | 93667337 | |||||||
chr11:93668000 | TC | T | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.309+195delC | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr11 | 93668000 | ||||||
chr11:93668027 | A | G | 96 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(93): Show |
100 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.309+220A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668027 | |||||||
chr11:93668242 | C | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.309+435C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668242 | |||||||
chr11:93668426 | A | G | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.310-382A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668426 | |||||||
chr11:93668452 | CA | C | 3 | a0005c0011t0001g0242 a0005c0011t0001g0244 a0014c0023t0001g0243 |
3 | HG01255.hp1 HG01891.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.310-354delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr11 | 93668452 | ||||||
chr11:93668454 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.310-354A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668454 | |||||||
chr11:93668525 | C | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.310-283C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668525 | |||||||
chr11:93668649 | A | G | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.310-159A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668649 | |||||||
chr11:93668653 | C | T | 55 | a0003c0002t0001g0001 a0003c0002t0001g0006 a0003c0002t0001g0078 others(52): Show |
65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.310-155C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 3/29 | chr11 | 93668653 | |||||||
chr11:93669260 | G | A | 3 | a0002c0003t0001g0023 a0002c0003t0001g0287 a0002c0003t0001g0288 |
4 | HG01891.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.434+328G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/29 | chr11 | 93669260 | |||||||
chr11:93669414 | G | GT | 164 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(161): Show |
178 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.435-250dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr11 | 93669414 | ||||||
chr11:93669469 | C | G | 2 | a0005c0006t0001g0042 a0005c0006t0001g0043 |
2 | HG00741.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-208C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/29 | chr11 | 93669469 | |||||||
chr11:93669527 | A | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.435-150A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 4/29 | chr11 | 93669527 | |||||||
chr11:93669779 | G | A | 18 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0025 others(15): Show |
21 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.528+9G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93669779 | |||||||
chr11:93669901 | G | A | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.528+131G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93669901 | |||||||
chr11:93669932 | A | G | 1 | a0009c0017t0002g0307 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.528+162A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93669932 | |||||||
chr11:93669945 | T | C | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.528+175T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93669945 | |||||||
chr11:93670180 | C | T | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.528+410C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670180 | |||||||
chr11:93670268 | A | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.528+498A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670268 | |||||||
chr11:93670323 | T | A | 90 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(87): Show |
94 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.528+553T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670323 | |||||||
chr11:93670397 | T | A | 2 | a0002c0010t0001g0022 a0002c0010t0001g0286 |
3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.528+627T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670397 | |||||||
chr11:93670397 | TA | T | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.528+634delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93670397 | ||||||
chr11:93670710 | G | A | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.528+940G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670710 | |||||||
chr11:93670812 | A | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.528+1042A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670812 | |||||||
chr11:93670888 | CT | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.528+1125delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93670888 | ||||||
chr11:93670895 | T | G | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.528+1125T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670895 | |||||||
chr11:93670968 | T | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.528+1198T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670968 | |||||||
chr11:93670985 | C | T | 1 | a0002c0003t0001g0288 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.528+1215C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93670985 | |||||||
chr11:93671046 | C | G | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.528+1276C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671046 | |||||||
chr11:93671111 | G | C | 5 | a0007c0007t0001g0071 a0007c0007t0001g0072 a0007c0007t0001g0074 others(2): Show |
5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+1341G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671111 | |||||||
chr11:93671315 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG00140.hp2 HG01516.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.528+1545C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671315 | |||||||
chr11:93671353 | T | C | 5 | a0007c0007t0001g0071 a0007c0007t0001g0072 a0007c0007t0001g0074 others(2): Show |
5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+1583T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671353 | |||||||
chr11:93671442 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.528+1672C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671442 | |||||||
chr11:93671458 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.528+1688G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671458 | |||||||
chr11:93671758 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.528+1988G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671758 | |||||||
chr11:93671771 | A | G | 1 | a0009c0017t0002g0307 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.528+2001A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671771 | |||||||
chr11:93671773 | G | T | 3 | a0005c0006t0001g0061 a0013c0034t0001g0059 a0019c0035t0001g0060 |
3 | HG01109.hp1 HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.528+2003G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671773 | |||||||
chr11:93671774 | C | T | 3 | a0005c0006t0001g0061 a0013c0034t0001g0059 a0019c0035t0001g0060 |
3 | HG01109.hp1 HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.528+2004C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671774 | |||||||
chr11:93671909 | G | A | 1 | a0002c0003t0001g0289 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.528+2139G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671909 | |||||||
chr11:93671965 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.528+2195G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93671965 | |||||||
chr11:93672124 | T | C | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.528+2354T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672124 | |||||||
chr11:93672216 | C | T | 1 | a0002c0003t0001g0285 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.528+2446C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672216 | |||||||
chr11:93672253 | A | G | 2 | a0004c0005t0003g0026 a0004c0047t0001g0249 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.528+2483A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672253 | |||||||
chr11:93672356 | G | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.528+2586G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672356 | |||||||
chr11:93672416 | C | CT | 15 | a0005c0026t0001g0044 a0006c0004t0001g0002 a0006c0004t0001g0027 others(12): Show |
19 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.528+2659dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93672416 | ||||||
chr11:93672435 | G | A | 1 | a0003c0002t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.528+2665G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672435 | |||||||
chr11:93672567 | A | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.528+2797A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672567 | |||||||
chr11:93672670 | A | G | 2 | a0002c0010t0001g0022 a0002c0010t0001g0286 |
3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.528+2900A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672670 | |||||||
chr11:93672734 | A | C | 1 | a0018c0038t0001g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.529-2837A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672734 | |||||||
chr11:93672832 | TATAATC | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.529-2737_529-2732d others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93672832 | ||||||
chr11:93672897 | A | C | 17 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(14): Show |
17 | HG00140.hp2 HG01099.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.529-2674A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672897 | |||||||
chr11:93672932 | G | GGTACTTT others(4): Show |
1 | a0004c0043t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.529-2630_529-2629i others(13): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93672932 | ||||||
chr11:93672949 | A | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.529-2622A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672949 | |||||||
chr11:93672981 | C | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.529-2590C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93672981 | |||||||
chr11:93673116 | T | A | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.529-2455T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673116 | |||||||
chr11:93673199 | T | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.529-2372T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673199 | |||||||
chr11:93673238 | C | G | 1 | a0015c0024t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.529-2333C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673238 | |||||||
chr11:93673451 | A | G | 1 | a0017c0041t0001g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.529-2120A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673451 | |||||||
chr11:93673481 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.529-2090T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673481 | |||||||
chr11:93673543 | G | T | 1 | a0004c0005t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.529-2028G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673543 | |||||||
chr11:93673597 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.529-1974G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673597 | |||||||
chr11:93673603 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.529-1968C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673603 | |||||||
chr11:93673689 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.529-1882C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673689 | |||||||
chr11:93673784 | C | T | 293 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.529-1787C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673784 | |||||||
chr11:93673848 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0271 |
3 | NA18966.hp2 NA18990.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.529-1723C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673848 | |||||||
chr11:93673943 | T | TC | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
245 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.529-1622dupC | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93673943 | ||||||
chr11:93673950 | T | C | 55 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0181 others(52): Show |
65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.529-1621T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673950 | |||||||
chr11:93673952 | C | T | 55 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0181 others(52): Show |
65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.529-1619C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673952 | |||||||
chr11:93673953 | T | C | 55 | a0001c0001t0001g0046 a0001c0001t0001g0069 a0001c0001t0001g0181 others(52): Show |
65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.529-1618T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673953 | |||||||
chr11:93673991 | C | T | 1 | a0005c0006t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.529-1580C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93673991 | |||||||
chr11:93674051 | C | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.529-1520C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674051 | |||||||
chr11:93674087 | C | T | 1 | a0023c0022t0001g0246 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.529-1484C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674087 | |||||||
chr11:93674225 | A | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.529-1346A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674225 | |||||||
chr11:93674252 | C | T | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.529-1319C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674252 | |||||||
chr11:93674496 | A | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.529-1075A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674496 | |||||||
chr11:93674603 | A | T | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.529-968A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674603 | |||||||
chr11:93674676 | T | G | 4 | a0009c0017t0002g0304 a0009c0017t0002g0307 a0011c0018t0001g0305 others(1): Show |
4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-895T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674676 | |||||||
chr11:93674682 | G | GT | 11 | a0001c0001t0001g0017 a0001c0001t0001g0229 a0001c0001t0001g0230 others(8): Show |
12 | HG01109.hp2 HG01192.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.529-885dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93674682 | ||||||
chr11:93674773 | T | C | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.529-798T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674773 | |||||||
chr11:93674775 | C | T | 1 | a0017c0041t0001g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.529-796C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674775 | |||||||
chr11:93674783 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.529-788A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674783 | |||||||
chr11:93674789 | T | A | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.529-782T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674789 | |||||||
chr11:93674877 | G | A | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.529-694G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674877 | |||||||
chr11:93674918 | A | G | 51 | a0003c0002t0001g0001 a0003c0002t0001g0006 a0003c0002t0001g0078 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.529-653A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93674918 | |||||||
chr11:93675161 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.529-410C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93675161 | |||||||
chr11:93675318 | T | TA | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.529-248dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93675318 | ||||||
chr11:93675438 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.529-133A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | chr11 | 93675438 | |||||||
chr11:93675562 | CTT | C | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.529-6_529-5delTT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr11 | 93675562 | ||||||
chr11:93675792 | C | CA | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.624+130dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr11 | 93675792 | ||||||
chr11:93676025 | A | G | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.624+359A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676025 | |||||||
chr11:93676049 | A | G | 2 | a0005c0006t0001g0041 a0016c0028t0001g0040 |
2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.624+383A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676049 | |||||||
chr11:93676107 | A | C | 1 | a0001c0001t0001g0227 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.624+441A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676107 | |||||||
chr11:93676174 | C | T | 4 | a0004c0009t0001g0036 a0004c0009t0001g0037 a0004c0009t0001g0121 others(1): Show |
4 | HG02055.hp1 HG03130.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+508C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676174 | |||||||
chr11:93676282 | A | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.624+616A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676282 | |||||||
chr11:93676396 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.624+730A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676396 | |||||||
chr11:93676448 | C | T | 2 | a0002c0019t0001g0282 a0002c0019t0001g0283 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.624+782C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676448 | |||||||
chr11:93676608 | A | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | NA18953.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.624+942A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676608 | |||||||
chr11:93676613 | T | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0256 others(11): Show |
19 | HG00438.hp1 HG01081.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.624+947T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676613 | |||||||
chr11:93676638 | G | A | 293 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.624+972G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676638 | |||||||
chr11:93676685 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.624+1019T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676685 | |||||||
chr11:93676692 | C | G | 1 | a0011c0018t0001g0306 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.624+1026C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676692 | |||||||
chr11:93676815 | A | T | 1 | a0003c0002t0001g0120 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.624+1149A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676815 | |||||||
chr11:93676879 | G | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.624+1213G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676879 | |||||||
chr11:93676918 | G | A | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.624+1252G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93676918 | |||||||
chr11:93677132 | C | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.624+1466C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677132 | |||||||
chr11:93677190 | T | C | 3 | a0004c0009t0001g0036 a0004c0009t0001g0037 a0004c0009t0001g0121 |
3 | HG03130.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.624+1524T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677190 | |||||||
chr11:93677370 | A | G | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.624+1704A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677370 | |||||||
chr11:93677414 | A | T | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+1748A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677414 | |||||||
chr11:93677521 | C | T | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.624+1855C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677521 | |||||||
chr11:93677560 | C | T | 1 | a0008c0008t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.625-1852C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677560 | |||||||
chr11:93677694 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.625-1718G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677694 | |||||||
chr11:93677987 | A | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.625-1425A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93677987 | |||||||
chr11:93678083 | T | A | 1 | a0031c0044t0001g0080 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.625-1329T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678083 | |||||||
chr11:93678097 | T | C | 1 | a0005c0006t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.625-1315T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678097 | |||||||
chr11:93678292 | C | T | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.625-1120C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678292 | |||||||
chr11:93678665 | C | T | 1 | a0004c0043t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.625-747C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678665 | |||||||
chr11:93678681 | G | A | 1 | a0003c0002t0001g0081 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.625-731G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678681 | |||||||
chr11:93678733 | G | A | 96 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(93): Show |
100 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.625-679G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678733 | |||||||
chr11:93678880 | G | A | 17 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0025 others(14): Show |
20 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.625-532G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678880 | |||||||
chr11:93678882 | A | T | 2 | a0002c0010t0001g0022 a0002c0010t0001g0286 |
3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.625-530A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93678882 | |||||||
chr11:93679046 | A | G | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.625-366A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679046 | |||||||
chr11:93679232 | A | C | 1 | a0031c0044t0001g0080 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.625-180A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679232 | |||||||
chr11:93679267 | C | T | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.625-145C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679267 | |||||||
chr11:93679329 | T | A | 1 | a0031c0044t0001g0080 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.625-83T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679329 | |||||||
chr11:93679364 | T | C | 7 | a0002c0003t0001g0024 a0002c0003t0001g0289 a0002c0003t0001g0290 others(4): Show |
8 | HG01074.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.625-48T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679364 | |||||||
chr11:93679408 | C | G | 1 | a0021c0040t0004g0294 | 1 | HG03579.hp2 | splice_region_variant&intron_variant | LOW | c.625-4C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 6/29 | chr11 | 93679408 | |||||||
chr11:93679563 | T | C | 4 | a0004c0005t0001g0083 a0008c0008t0001g0010 a0008c0008t0001g0082 others(1): Show |
5 | HG02451.hp1 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.765+11T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93679563 | |||||||
chr11:93679608 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.765+56A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93679608 | |||||||
chr11:93679660 | T | C | 52 | a0001c0001t0001g0124 a0003c0002t0001g0001 a0003c0002t0001g0006 others(49): Show |
62 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.765+108T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93679660 | |||||||
chr11:93679892 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.765+340T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93679892 | |||||||
chr11:93679967 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.765+415C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93679967 | |||||||
chr11:93680005 | G | A | 2 | a0005c0006t0001g0268 a0005c0006t0001g0269 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.765+453G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680005 | |||||||
chr11:93680201 | C | T | 3 | a0001c0001t0001g0179 a0002c0010t0001g0022 a0002c0010t0001g0286 |
4 | HG01884.hp2 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+649C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680201 | |||||||
chr11:93680287 | A | G | 1 | a0008c0008t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.765+735A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680287 | |||||||
chr11:93680319 | C | T | 3 | a0002c0019t0001g0282 a0002c0019t0001g0283 a0017c0041t0001g0284 |
3 | HG02723.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.765+767C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680319 | |||||||
chr11:93680537 | T | C | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.765+985T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680537 | |||||||
chr11:93680655 | C | A | 7 | a0002c0003t0001g0024 a0002c0003t0001g0289 a0002c0003t0001g0290 others(4): Show |
8 | HG01074.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.765+1103C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680655 | |||||||
chr11:93680691 | G | A | 293 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.765+1139G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680691 | |||||||
chr11:93680796 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.765+1244A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93680796 | |||||||
chr11:93681004 | G | A | 3 | a0008c0008t0001g0010 a0008c0008t0001g0082 a0008c0008t0001g0119 |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+1452G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681004 | |||||||
chr11:93681090 | C | A | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.765+1538C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681090 | |||||||
chr11:93681141 | A | G | 2 | a0013c0034t0001g0059 a0019c0035t0001g0060 |
2 | HG01109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.765+1589A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681141 | |||||||
chr11:93681235 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765+1683T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681235 | |||||||
chr11:93681237 | GT | G | 167 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(164): Show |
185 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.765+1702delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681237 | ||||||
chr11:93681240 | T | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
124 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.765+1688T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681240 | |||||||
chr11:93681241 | T | G | 167 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(164): Show |
185 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.765+1689T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681241 | |||||||
chr11:93681242 | T | G | 1 | a0031c0044t0001g0080 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.765+1690T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681242 | |||||||
chr11:93681276 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
6 | NA18971.hp1 NA18972.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.765+1724G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681276 | |||||||
chr11:93681403 | A | AT | 18 | a0002c0003t0001g0020 a0002c0003t0001g0025 a0002c0003t0001g0275 others(15): Show |
24 | HG01074.hp2 HG01361.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.765+1881dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | ||||||
chr11:93681403 | A | ATT | 40 | a0001c0001t0001g0070 a0001c0001t0001g0186 a0002c0003t0001g0021 others(37): Show |
51 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.765+1880_765+1881d others(4): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | ||||||
chr11:93681403 | A | ATTT | 65 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0068 others(62): Show |
67 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.765+1879_765+1881d others(5): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | ||||||
chr11:93681403 | A | ATTTT | 60 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(57): Show |
62 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.765+1878_765+1881d others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | ||||||
chr11:93681403 | A | ATTTTT | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(45): Show |
61 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.765+1877_765+1881d others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | ||||||
chr11:93681403 | A | ATTTTTT | 44 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(41): Show |
50 | HG00438.hp1 HG00741.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.765+1876_765+1881d others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | ||||||
chr11:93681403 | A | ATTTTTTT | 12 | a0001c0001t0001g0053 a0001c0001t0001g0057 a0001c0001t0001g0058 others(9): Show |
12 | HG01099.hp2 HG01358.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.765+1875_765+1881d others(9): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | ||||||
chr11:93681403 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0064 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.765+1872_765+1881d others(12): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | ||||||
chr11:93681403 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0127 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.765+1871_765+1881d others(13): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681403 | ||||||
chr11:93681463 | G | T | 291 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.765+1911G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681463 | |||||||
chr11:93681472 | A | G | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(271): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.765+1920A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681472 | |||||||
chr11:93681477 | G | A | 7 | a0002c0003t0001g0274 a0005c0006t0001g0039 a0005c0006t0001g0041 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.765+1925G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681477 | |||||||
chr11:93681517 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.765+1965A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681517 | |||||||
chr11:93681693 | C | T | 1 | a0030c0031t0001g0224 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.766-1866C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681693 | |||||||
chr11:93681786 | A | G | 1 | a0014c0023t0001g0243 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.766-1773A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681786 | |||||||
chr11:93681860 | G | GT | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.766-1687dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93681860 | ||||||
chr11:93681865 | T | TG | 89 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(86): Show |
93 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.766-1694_766-1693i others(3): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681865 | |||||||
chr11:93681920 | A | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.766-1639A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681920 | |||||||
chr11:93681921 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.766-1638A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681921 | |||||||
chr11:93681924 | A | G | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 |
3 | HG02922.hp2 HG03195.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.766-1635A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93681924 | |||||||
chr11:93682127 | A | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.766-1432A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93682127 | |||||||
chr11:93682458 | A | G | 2 | a0010c0020t0001g0084 a0010c0020t0001g0099 |
2 | HG02683.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.766-1101A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93682458 | |||||||
chr11:93682538 | T | A | 1 | a0002c0003t0001g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766-1021T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93682538 | |||||||
chr11:93682596 | TA | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.766-952delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr11 | 93682596 | ||||||
chr11:93682674 | A | T | 68 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(65): Show |
71 | HG00323.hp2 HG00438.hp2 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.766-885A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93682674 | |||||||
chr11:93682821 | C | T | 1 | a0004c0005t0001g0098 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.766-738C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93682821 | |||||||
chr11:93683059 | T | G | 18 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0025 others(15): Show |
21 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.766-500T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683059 | |||||||
chr11:93683142 | C | T | 1 | a0005c0011t0001g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766-417C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683142 | |||||||
chr11:93683305 | C | A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0212 others(1): Show |
4 | HG02148.hp1 HG02257.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-254C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683305 | |||||||
chr11:93683346 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.766-213A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683346 | |||||||
chr11:93683367 | G | T | 1 | a0004c0043t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-192G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683367 | |||||||
chr11:93683495 | C | T | 1 | a0002c0003t0001g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.766-64C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 7/29 | chr11 | 93683495 | |||||||
chr11:93683797 | A | G | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.949+55A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 8/29 | chr11 | 93683797 | |||||||
chr11:93683948 | A | G | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.950-16A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 8/29 | chr11 | 93683948 | |||||||
chr11:93684145 | G | A | 2 | a0013c0034t0001g0059 a0019c0035t0001g0060 |
2 | HG01109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1114+17G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684145 | |||||||
chr11:93684271 | C | T | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1114+143C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684271 | |||||||
chr11:93684294 | C | T | 55 | a0003c0002t0001g0001 a0003c0002t0001g0006 a0003c0002t0001g0078 others(52): Show |
65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1114+166C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684294 | |||||||
chr11:93684295 | G | A | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1114+167G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684295 | |||||||
chr11:93684343 | G | C | 1 | a0004c0005t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1114+215G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684343 | |||||||
chr11:93684624 | G | A | 1 | a0004c0005t0001g0101 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1114+496G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684624 | |||||||
chr11:93684638 | G | A | 3 | a0002c0003t0001g0021 a0002c0003t0001g0275 a0002c0003t0001g0285 |
4 | HG01081.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114+510G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684638 | |||||||
chr11:93684693 | C | T | 90 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(87): Show |
94 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1114+565C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684693 | |||||||
chr11:93684809 | C | G | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0220 |
3 | HG01516.hp2 HG01943.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1114+681C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684809 | |||||||
chr11:93684848 | G | A | 300 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(297): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1114+720G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684848 | |||||||
chr11:93684898 | C | T | 1 | a0005c0006t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1114+770C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684898 | |||||||
chr11:93684965 | T | C | 3 | a0001c0001t0001g0181 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | NA18941.hp2 NA18990.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1114+837T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93684965 | |||||||
chr11:93685028 | A | C | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1114+900A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685028 | |||||||
chr11:93685200 | A | G | 1 | a0005c0006t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1114+1072A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685200 | |||||||
chr11:93685231 | T | C | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1114+1103T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685231 | |||||||
chr11:93685366 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1114+1238C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685366 | |||||||
chr11:93685398 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0239 |
2 | NA18988.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1114+1270G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685398 | |||||||
chr11:93685403 | C | T | 47 | a0003c0002t0001g0001 a0003c0002t0001g0006 a0003c0002t0001g0078 others(44): Show |
56 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.1114+1275C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685403 | |||||||
chr11:93685525 | A | G | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1114+1397A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685525 | |||||||
chr11:93685531 | A | C | 1 | a0005c0006t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1114+1403A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685531 | |||||||
chr11:93685538 | G | GA | 7 | a0002c0003t0001g0024 a0002c0003t0001g0289 a0002c0003t0001g0290 others(4): Show |
8 | HG01074.hp2 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114+1418dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93685538 | ||||||
chr11:93685575 | T | A | 1 | a0004c0005t0001g0101 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1114+1447T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685575 | |||||||
chr11:93685593 | A | G | 291 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1114+1465A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685593 | |||||||
chr11:93685609 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1114+1481A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685609 | |||||||
chr11:93685686 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1114+1558C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685686 | |||||||
chr11:93685700 | C | CTTTG | 147 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(144): Show |
160 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1114+1596_1114+159 others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93685700 | ||||||
chr11:93685700 | C | CTTTGTTT others(1): Show |
108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
128 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1114+1592_1114+159 others(12): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93685700 | ||||||
chr11:93685700 | C | CTTTGTTT others(5): Show |
4 | a0001c0001t0001g0132 a0001c0001t0001g0164 a0001c0001t0001g0233 others(1): Show |
4 | NA19011.hp1 NA19057.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+1588_1114+159 others(16): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93685700 | ||||||
chr11:93685774 | G | A | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.1114+1646G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685774 | |||||||
chr11:93685804 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1114+1676G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685804 | |||||||
chr11:93685841 | G | GAGAGATT others(885): Show |
6 | a0001c0001t0001g0018 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1713_1114+171 others(896): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685841 | |||||||
chr11:93685844 | G | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1716G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685844 | |||||||
chr11:93685845 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1717G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685845 | |||||||
chr11:93685847 | A | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1719A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685847 | |||||||
chr11:93685849 | TACA | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1722_1114+172 others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685849 | |||||||
chr11:93685853 | G | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
7 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+1725G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685853 | |||||||
chr11:93685931 | G | A | 1 | a0004c0009t0001g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1115-1713G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685931 | |||||||
chr11:93685949 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1115-1695C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93685949 | |||||||
chr11:93686229 | T | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1115-1415T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686229 | |||||||
chr11:93686288 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1115-1356C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686288 | |||||||
chr11:93686319 | T | TA | 295 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1115-1313dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93686319 | ||||||
chr11:93686319 | T | TAA | 13 | a0001c0001t0001g0225 a0003c0002t0001g0117 a0005c0026t0001g0044 others(10): Show |
17 | HG02165.hp1 HG03098.hp2 HG03453.hp1 others(14): Show |
intron_variant | MODIFIER | c.1115-1314_1115-131 others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr11 | 93686319 | ||||||
chr11:93686337 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1115-1307T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686337 | |||||||
chr11:93686352 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1115-1292C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686352 | |||||||
chr11:93686665 | A | G | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1115-979A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686665 | |||||||
chr11:93686682 | A | G | 5 | a0005c0033t0001g0038 a0009c0017t0002g0304 a0009c0017t0002g0307 others(2): Show |
5 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1115-962A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686682 | |||||||
chr11:93686796 | T | C | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1115-848T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686796 | |||||||
chr11:93686953 | T | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1115-691T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93686953 | |||||||
chr11:93687156 | C | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1115-488C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687156 | |||||||
chr11:93687194 | C | T | 1 | a0018c0038t0001g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1115-450C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687194 | |||||||
chr11:93687218 | A | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1115-426A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687218 | |||||||
chr11:93687379 | A | G | 1 | a0005c0006t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1115-265A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687379 | |||||||
chr11:93687399 | A | G | 51 | a0003c0002t0001g0001 a0003c0002t0001g0006 a0003c0002t0001g0078 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1115-245A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687399 | |||||||
chr11:93687525 | G | C | 1 | a0001c0001t0001g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1115-119G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 9/29 | chr11 | 93687525 | |||||||
chr11:93688335 | A | G | 1 | a0005c0011t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1336+470A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688335 | |||||||
chr11:93688399 | T | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1336+534T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688399 | |||||||
chr11:93688434 | G | A | 5 | a0007c0007t0001g0071 a0007c0007t0001g0072 a0007c0007t0001g0074 others(2): Show |
5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336+569G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688434 | |||||||
chr11:93688460 | A | G | 1 | a0030c0031t0001g0224 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1336+595A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688460 | |||||||
chr11:93688533 | C | G | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1336+668C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688533 | |||||||
chr11:93688577 | TG | T | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1336+714delG | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93688577 | ||||||
chr11:93688593 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0126 a0001c0001t0001g0156 others(1): Show |
6 | HG02080.hp1 NA18942.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1336+728C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688593 | |||||||
chr11:93688616 | G | A | 90 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(87): Show |
94 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1336+751G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688616 | |||||||
chr11:93688644 | A | C | 1 | a0004c0043t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1336+779A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688644 | |||||||
chr11:93688671 | C | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1336+806C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688671 | |||||||
chr11:93688681 | C | T | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1336+816C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688681 | |||||||
chr11:93688984 | G | C | 1 | a0003c0002t0001g0078 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1336+1119G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688984 | |||||||
chr11:93688999 | T | C | 3 | a0004c0009t0001g0036 a0004c0009t0001g0037 a0004c0009t0001g0121 |
3 | HG03130.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1336+1134T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93688999 | |||||||
chr11:93689204 | A | G | 4 | a0002c0003t0001g0020 a0002c0003t0001g0274 a0002c0003t0001g0277 others(1): Show |
5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336+1339A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93689204 | |||||||
chr11:93689286 | G | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1336+1421G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93689286 | |||||||
chr11:93689447 | G | A | 88 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(85): Show |
92 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1336+1582G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93689447 | |||||||
chr11:93689545 | A | C | 1 | a0001c0001t0001g0237 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1336+1680A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93689545 | |||||||
chr11:93689886 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1337-1797G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93689886 | |||||||
chr11:93690071 | G | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1337-1612G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690071 | |||||||
chr11:93690267 | C | T | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1337-1416C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690267 | |||||||
chr11:93690299 | C | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1337-1384C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690299 | |||||||
chr11:93690431 | T | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1337-1252T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690431 | |||||||
chr11:93690513 | C | T | 5 | a0007c0007t0001g0071 a0007c0007t0001g0072 a0007c0007t0001g0074 others(2): Show |
5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1337-1170C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690513 | |||||||
chr11:93690519 | A | G | 4 | a0009c0017t0002g0304 a0009c0017t0002g0307 a0011c0018t0001g0305 others(1): Show |
4 | HG01099.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1337-1164A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690519 | |||||||
chr11:93690553 | T | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1337-1130T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690553 | |||||||
chr11:93690560 | C | CA | 26 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0065 others(23): Show |
26 | HG01168.hp2 HG01169.hp2 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.1337-1102dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93690560 | ||||||
chr11:93690560 | CA | C | 46 | a0003c0002t0001g0001 a0003c0002t0001g0006 a0003c0002t0001g0078 others(43): Show |
56 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.1337-1102delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93690560 | ||||||
chr11:93690635 | G | A | 1 | a0003c0002t0001g0104 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1337-1048G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690635 | |||||||
chr11:93690729 | C | CA | 8 | a0002c0003t0001g0024 a0002c0003t0001g0289 a0002c0003t0001g0290 others(5): Show |
9 | HG00609.hp2 HG01074.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1337-930dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93690729 | ||||||
chr11:93690729 | CA | C | 57 | a0001c0001t0001g0015 a0001c0001t0001g0067 a0001c0001t0001g0068 others(54): Show |
63 | HG00408.hp2 HG00558.hp2 HG01081.hp1 others(60): Show |
intron_variant | MODIFIER | c.1337-930delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93690729 | ||||||
chr11:93690729 | CAA | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1337-931_1337-930d others(4): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93690729 | ||||||
chr11:93690752 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1337-931A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690752 | |||||||
chr11:93690851 | T | C | 1 | a0002c0003t0001g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1337-832T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690851 | |||||||
chr11:93690874 | T | G | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1337-809T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690874 | |||||||
chr11:93690878 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1337-805C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690878 | |||||||
chr11:93690895 | T | C | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1337-788T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93690895 | |||||||
chr11:93691018 | G | A | 4 | a0002c0003t0001g0020 a0002c0003t0001g0274 a0002c0003t0001g0277 others(1): Show |
5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1337-665G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691018 | |||||||
chr11:93691069 | T | C | 1 | a0023c0022t0001g0246 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1337-614T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691069 | |||||||
chr11:93691103 | T | G | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1337-580T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691103 | |||||||
chr11:93691113 | A | T | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1337-570A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691113 | |||||||
chr11:93691181 | T | TCTGC | 18 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0025 others(15): Show |
21 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1337-500_1337-497d others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr11 | 93691181 | ||||||
chr11:93691277 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG02148.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1337-406G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691277 | |||||||
chr11:93691288 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1337-395C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691288 | |||||||
chr11:93691478 | A | G | 4 | a0005c0006t0001g0039 a0005c0006t0001g0268 a0005c0006t0001g0269 others(1): Show |
4 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1337-205A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691478 | |||||||
chr11:93691503 | A | G | 1 | a0001c0013t0001g0205 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1337-180A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 10/29 | chr11 | 93691503 | |||||||
chr11:93692173 | A | AT | 7 | a0005c0014t0001g0076 a0005c0014t0001g0077 a0007c0007t0001g0071 others(4): Show |
7 | HG02004.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533+144dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr11 | 93692173 | ||||||
chr11:93692199 | A | G | 1 | a0005c0014t0001g0076 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1533+169A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692199 | |||||||
chr11:93692232 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1533+202T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692232 | |||||||
chr11:93692426 | A | G | 2 | a0013c0034t0001g0059 a0019c0035t0001g0060 |
2 | HG01109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1533+396A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692426 | |||||||
chr11:93692482 | G | A | 1 | a0004c0043t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1533+452G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692482 | |||||||
chr11:93692498 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0149 |
2 | NA18962.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1533+468G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692498 | |||||||
chr11:93692689 | T | C | 19 | a0001c0001t0001g0015 a0001c0001t0001g0067 a0001c0001t0001g0068 others(16): Show |
20 | HG00408.hp2 HG00621.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.1533+659T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692689 | |||||||
chr11:93692920 | T | TC | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1533+891dupC | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr11 | 93692920 | ||||||
chr11:93692942 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1533+912C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692942 | |||||||
chr11:93692972 | C | CA | 11 | a0001c0001t0001g0052 a0001c0001t0001g0156 a0001c0001t0001g0228 others(8): Show |
11 | HG02055.hp1 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1533+960dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr11 | 93692972 | ||||||
chr11:93692972 | CA | C | 13 | a0001c0001t0001g0131 a0001c0001t0001g0231 a0002c0019t0001g0282 others(10): Show |
17 | HG01168.hp2 HG02165.hp1 NA18940.hp2 others(14): Show |
intron_variant | MODIFIER | c.1533+960delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr11 | 93692972 | ||||||
chr11:93692983 | A | C | 51 | a0003c0002t0001g0001 a0003c0002t0001g0006 a0003c0002t0001g0078 others(48): Show |
61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.1533+953A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93692983 | |||||||
chr11:93693104 | CG | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1533+1075delG | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693104 | |||||||
chr11:93693106 | T | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1533+1076T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693106 | |||||||
chr11:93693145 | C | T | 1 | a0002c0003t0001g0293 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1533+1115C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693145 | |||||||
chr11:93693149 | C | T | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1533+1119C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693149 | |||||||
chr11:93693193 | T | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1533+1163T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693193 | |||||||
chr11:93693230 | T | C | 2 | a0003c0002t0001g0081 a0003c0002t0001g0105 |
2 | NA18991.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1533+1200T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693230 | |||||||
chr11:93693234 | G | T | 1 | a0001c0001t0001g0155 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1533+1204G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693234 | |||||||
chr11:93693288 | A | G | 1 | a0002c0003t0001g0299 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1533+1258A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693288 | |||||||
chr11:93693354 | C | A | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1533+1324C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693354 | |||||||
chr11:93693492 | A | G | 1 | a0002c0003t0001g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1533+1462A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693492 | |||||||
chr11:93693495 | T | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1533+1465T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693495 | |||||||
chr11:93693542 | G | C | 1 | a0005c0006t0001g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1533+1512G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693542 | |||||||
chr11:93693585 | A | C | 1 | a0023c0022t0001g0246 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1533+1555A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693585 | |||||||
chr11:93693616 | C | T | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1533+1586C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693616 | |||||||
chr11:93693687 | T | G | 1 | a0001c0001t0001g0197 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1533+1657T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693687 | |||||||
chr11:93693720 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1533+1690C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693720 | |||||||
chr11:93693787 | C | G | 3 | a0002c0003t0001g0024 a0002c0003t0001g0290 a0002c0003t0001g0291 |
4 | HG02258.hp2 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534-1710C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693787 | |||||||
chr11:93693972 | A | G | 1 | a0004c0043t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1534-1525A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93693972 | |||||||
chr11:93694127 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1534-1370G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694127 | |||||||
chr11:93694291 | A | G | 2 | a0002c0010t0001g0022 a0002c0010t0001g0286 |
3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1534-1206A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694291 | |||||||
chr11:93694302 | G | A | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1534-1195G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694302 | |||||||
chr11:93694422 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1534-1075A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694422 | |||||||
chr11:93694710 | A | G | 1 | a0007c0007t0001g0075 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1534-787A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694710 | |||||||
chr11:93694721 | G | A | 14 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(11): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.1534-776G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694721 | |||||||
chr11:93694775 | T | C | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.1534-722T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93694775 | |||||||
chr11:93695125 | A | T | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1534-372A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93695125 | |||||||
chr11:93695341 | T | C | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1534-156T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93695341 | |||||||
chr11:93695393 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1534-104G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93695393 | |||||||
chr11:93695478 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1534-19A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 12/29 | chr11 | 93695478 | |||||||
chr11:93695679 | G | T | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.1671+45G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 13/29 | chr11 | 93695679 | |||||||
chr11:93695941 | G | A | 2 | a0001c0001t0001g0125 a0001c0016t0001g0012 |
3 | NA18956.hp1 NA19077.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1671+307G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 13/29 | chr11 | 93695941 | |||||||
chr11:93696069 | G | A | 13 | a0002c0003t0001g0021 a0002c0003t0001g0025 a0002c0003t0001g0275 others(10): Show |
15 | HG01081.hp1 HG01192.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1672-251G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 13/29 | chr11 | 93696069 | |||||||
chr11:93696162 | A | G | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1672-158A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 13/29 | chr11 | 93696162 | |||||||
chr11:93700424 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.5274+238T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700424 | |||||||
chr11:93700426 | C | CT | 44 | a0001c0001t0001g0154 a0001c0001t0001g0161 a0001c0001t0001g0176 others(41): Show |
50 | HG01074.hp2 HG01081.hp1 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.5274+257dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr11 | 93700426 | ||||||
chr11:93700426 | CT | C | 12 | a0005c0006t0001g0268 a0006c0004t0001g0002 a0006c0004t0001g0027 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG02895.hp2 others(13): Show |
intron_variant | MODIFIER | c.5274+257delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr11 | 93700426 | ||||||
chr11:93700600 | AT | A | 13 | a0005c0006t0001g0061 a0006c0004t0001g0002 a0006c0004t0001g0027 others(10): Show |
17 | HG01099.hp1 HG02055.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.5274+427delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr11 | 93700600 | ||||||
chr11:93700731 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5274+545A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700731 | |||||||
chr11:93700755 | T | A | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5274+569T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700755 | |||||||
chr11:93700757 | T | C | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5274+571T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700757 | |||||||
chr11:93700758 | T | C | 1 | a0014c0023t0001g0243 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5274+572T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700758 | |||||||
chr11:93700765 | T | G | 14 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(11): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.5274+579T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700765 | |||||||
chr11:93700824 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.5274+638T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700824 | |||||||
chr11:93700974 | A | G | 2 | a0002c0010t0001g0022 a0002c0010t0001g0286 |
3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5274+788A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700974 | |||||||
chr11:93700990 | C | CT | 14 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(11): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.5274+804_5274+805i others(3): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93700990 | |||||||
chr11:93701147 | C | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.5274+961C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701147 | |||||||
chr11:93701278 | T | A | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5274+1092T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701278 | |||||||
chr11:93701557 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.5275-903T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701557 | |||||||
chr11:93701649 | G | A | 14 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(11): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.5275-811G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701649 | |||||||
chr11:93701717 | C | T | 1 | a0003c0002t0001g0120 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5275-743C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701717 | |||||||
chr11:93701879 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5275-581G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93701879 | |||||||
chr11:93701935 | GGTTGTTG others(8): Show |
G | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG00438.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.5275-515_5275-501d others(17): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr11 | 93701935 | ||||||
chr11:93702108 | A | G | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5275-352A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93702108 | |||||||
chr11:93702389 | T | C | 1 | a0001c0012t0001g0180 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.5275-71T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 15/29 | chr11 | 93702389 | |||||||
chr11:93702747 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.5453-29T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 16/29 | chr11 | 93702747 | |||||||
chr11:93703088 | C | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.5596+169C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703088 | |||||||
chr11:93703109 | G | A | 91 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(88): Show |
95 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.5596+190G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703109 | |||||||
chr11:93703166 | A | G | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5596+247A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703166 | |||||||
chr11:93703335 | G | A | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5596+416G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703335 | |||||||
chr11:93703435 | A | G | 1 | a0004c0005t0001g0098 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5596+516A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703435 | |||||||
chr11:93703477 | T | C | 255 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.5596+558T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703477 | |||||||
chr11:93703480 | G | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.5596+561G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703480 | |||||||
chr11:93703544 | T | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0126 a0001c0001t0001g0134 others(9): Show |
14 | HG00673.hp2 HG02074.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.5596+625T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703544 | |||||||
chr11:93703575 | GT | G | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5596+668delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr11 | 93703575 | ||||||
chr11:93703624 | ACTGTT | A | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5596+713_5596+717d others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr11 | 93703624 | ||||||
chr11:93703675 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.5596+756G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703675 | |||||||
chr11:93703693 | A | G | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5596+774A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703693 | |||||||
chr11:93703767 | C | CT | 26 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(23): Show |
27 | HG00099.hp2 HG01074.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.5596+867dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr11 | 93703767 | ||||||
chr11:93703767 | CT | C | 10 | a0001c0001t0001g0049 a0001c0001t0001g0254 a0001c0001t0001g0258 others(7): Show |
10 | HG01168.hp1 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.5596+867delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr11 | 93703767 | ||||||
chr11:93703814 | G | A | 2 | a0002c0010t0001g0022 a0002c0010t0001g0286 |
3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5596+895G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703814 | |||||||
chr11:93703825 | G | A | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5596+906G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93703825 | |||||||
chr11:93704008 | A | T | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5596+1089A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704008 | |||||||
chr11:93704100 | T | C | 2 | a0003c0002t0001g0089 a0003c0002t0001g0106 |
2 | HG00673.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.5596+1181T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704100 | |||||||
chr11:93704134 | C | G | 1 | a0002c0003t0001g0298 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5596+1215C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704134 | |||||||
chr11:93704253 | A | C | 1 | a0003c0002t0001g0120 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5596+1334A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704253 | |||||||
chr11:93704398 | G | A | 1 | a0018c0038t0001g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5596+1479G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704398 | |||||||
chr11:93704405 | C | G | 1 | a0005c0006t0001g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5596+1486C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704405 | |||||||
chr11:93704411 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
6 | HG01192.hp2 HG01358.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.5596+1492C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704411 | |||||||
chr11:93704438 | C | A | 30 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0025 others(27): Show |
37 | HG01081.hp1 HG01099.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.5596+1519C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704438 | |||||||
chr11:93704783 | A | G | 3 | a0005c0011t0001g0242 a0005c0011t0001g0244 a0014c0023t0001g0243 |
3 | HG01255.hp1 HG01891.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.5596+1864A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704783 | |||||||
chr11:93704844 | C | G | 96 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(93): Show |
100 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.5597-1901C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704844 | |||||||
chr11:93704984 | C | T | 1 | a0019c0035t0001g0060 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5597-1761C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93704984 | |||||||
chr11:93705032 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5597-1713T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705032 | |||||||
chr11:93705039 | T | C | 1 | a0004c0043t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5597-1706T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705039 | |||||||
chr11:93705072 | A | G | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5597-1673A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705072 | |||||||
chr11:93705194 | C | T | 20 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(17): Show |
20 | HG00140.hp2 HG01099.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.5597-1551C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705194 | |||||||
chr11:93705195 | G | A | 14 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(11): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.5597-1550G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705195 | |||||||
chr11:93705202 | G | C | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5597-1543G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705202 | |||||||
chr11:93705289 | C | CAAAGCAC others(10): Show |
1 | a0001c0001t0001g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5597-1452_5597-143 others(21): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr11 | 93705289 | ||||||
chr11:93705444 | T | G | 4 | a0004c0005t0001g0083 a0008c0008t0001g0010 a0008c0008t0001g0082 others(1): Show |
5 | HG02451.hp1 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.5597-1301T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705444 | |||||||
chr11:93705789 | G | A | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5597-956G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705789 | |||||||
chr11:93705867 | C | G | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5597-878C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93705867 | |||||||
chr11:93706013 | G | A | 1 | a0002c0010t0001g0022 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5597-732G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706013 | |||||||
chr11:93706069 | G | A | 2 | a0010c0020t0001g0084 a0010c0020t0001g0099 |
2 | HG02683.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.5597-676G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706069 | |||||||
chr11:93706080 | G | T | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5597-665G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706080 | |||||||
chr11:93706166 | G | A | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5597-579G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706166 | |||||||
chr11:93706256 | C | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.5597-489C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706256 | |||||||
chr11:93706292 | A | G | 1 | a0002c0003t0001g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5597-453A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706292 | |||||||
chr11:93706295 | A | G | 1 | a0017c0041t0001g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5597-450A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706295 | |||||||
chr11:93706299 | A | G | 4 | a0002c0003t0001g0020 a0002c0003t0001g0274 a0002c0003t0001g0277 others(1): Show |
5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.5597-446A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706299 | |||||||
chr11:93706355 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0182 a0001c0001t0001g0184 others(1): Show |
5 | NA18971.hp1 NA18972.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.5597-390T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706355 | |||||||
chr11:93706394 | T | C | 6 | a0005c0006t0001g0039 a0005c0006t0001g0041 a0005c0006t0001g0268 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5597-351T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706394 | |||||||
chr11:93706636 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0127 |
3 | HG00741.hp1 HG01433.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.5597-109A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706636 | |||||||
chr11:93706727 | A | T | 1 | a0002c0003t0001g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5597-18A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706727 | |||||||
chr11:93706735 | T | C | 3 | a0003c0002t0001g0107 a0005c0014t0001g0076 a0005c0014t0001g0077 |
3 | HG02004.hp1 HG02280.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.5597-10T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 17/29 | chr11 | 93706735 | |||||||
chr11:93707040 | A | G | 2 | a0002c0019t0001g0282 a0002c0019t0001g0283 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5749+143A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707040 | |||||||
chr11:93707099 | C | CTTTTAAA others(11): Show |
3 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0172 |
3 | HG00140.hp2 HG01516.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.5749+202_5749+203i others(20): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707099 | |||||||
chr11:93707100 | C | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0172 |
3 | HG00140.hp2 HG01516.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.5749+203C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707100 | |||||||
chr11:93707135 | A | G | 54 | a0003c0002t0001g0001 a0003c0002t0001g0006 a0003c0002t0001g0078 others(51): Show |
64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.5749+238A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707135 | |||||||
chr11:93707295 | A | G | 2 | a0002c0010t0001g0022 a0002c0010t0001g0286 |
3 | HG01884.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.5749+398A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707295 | |||||||
chr11:93707441 | A | G | 1 | a0015c0024t0001g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.5749+544A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707441 | |||||||
chr11:93707490 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5749+593G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707490 | |||||||
chr11:93707530 | A | G | 3 | a0002c0003t0001g0024 a0002c0003t0001g0290 a0002c0003t0001g0291 |
4 | HG02258.hp2 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5749+633A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707530 | |||||||
chr11:93707564 | C | T | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+667C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707564 | |||||||
chr11:93707565 | C | A | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+668C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707565 | |||||||
chr11:93707583 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5749+686A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707583 | |||||||
chr11:93707842 | A | G | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5749+945A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707842 | |||||||
chr11:93707944 | T | G | 1 | a0002c0003t0001g0299 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5749+1047T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707944 | |||||||
chr11:93707992 | A | C | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+1095A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93707992 | |||||||
chr11:93708084 | T | C | 4 | a0003c0002t0001g0102 a0003c0002t0001g0108 a0003c0002t0001g0109 others(1): Show |
4 | NA18949.hp1 NA19000.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.5749+1187T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708084 | |||||||
chr11:93708167 | T | G | 1 | a0002c0003t0001g0295 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5749+1270T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708167 | |||||||
chr11:93708201 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5749+1304T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708201 | |||||||
chr11:93708206 | A | G | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5749+1309A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708206 | |||||||
chr11:93708308 | G | A | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+1411G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708308 | |||||||
chr11:93708512 | C | G | 5 | a0007c0007t0001g0071 a0007c0007t0001g0072 a0007c0007t0001g0074 others(2): Show |
5 | HG02145.hp2 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.5749+1615C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708512 | |||||||
chr11:93708521 | T | TA | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+1625dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93708521 | ||||||
chr11:93708526 | G | A | 1 | a0002c0003t0001g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5749+1629G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708526 | |||||||
chr11:93708670 | G | A | 6 | a0003c0002t0001g0090 a0003c0002t0001g0091 a0003c0002t0001g0092 others(3): Show |
6 | HG02015.hp2 HG02148.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.5749+1773G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708670 | |||||||
chr11:93708684 | G | A | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5749+1787G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708684 | |||||||
chr11:93708746 | C | T | 293 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.5749+1849C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708746 | |||||||
chr11:93708767 | C | T | 18 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0025 others(15): Show |
21 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.5749+1870C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708767 | |||||||
chr11:93708913 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5749+2016C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93708913 | |||||||
chr11:93709143 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0058 |
2 | HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.5749+2246A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709143 | |||||||
chr11:93709214 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.5749+2317C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709214 | |||||||
chr11:93709399 | A | T | 1 | a0005c0006t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5749+2502A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709399 | |||||||
chr11:93709476 | T | C | 305 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(302): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.5749+2579T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709476 | |||||||
chr11:93709816 | T | A | 3 | a0005c0011t0001g0242 a0005c0011t0001g0244 a0014c0023t0001g0243 |
3 | HG01255.hp1 HG01891.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.5749+2919T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709816 | |||||||
chr11:93709972 | T | A | 3 | a0004c0009t0001g0036 a0004c0009t0001g0037 a0004c0009t0001g0121 |
3 | HG03130.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5749+3075T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93709972 | |||||||
chr11:93710062 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.5749+3165T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710062 | |||||||
chr11:93710069 | G | A | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+3172G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710069 | |||||||
chr11:93710133 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0123 a0001c0001t0001g0132 others(5): Show |
11 | HG00323.hp1 HG00609.hp1 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.5749+3236C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710133 | |||||||
chr11:93710134 | G | A | 14 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(11): Show |
18 | HG01099.hp1 HG02165.hp1 HG02809.hp1 others(15): Show |
intron_variant | MODIFIER | c.5749+3237G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710134 | |||||||
chr11:93710139 | C | T | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+3242C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710139 | |||||||
chr11:93710209 | A | AGGAT | 6 | a0005c0006t0001g0039 a0005c0006t0001g0041 a0005c0006t0001g0268 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5749+3313_5749+331 others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93710209 | ||||||
chr11:93710211 | A | T | 6 | a0005c0006t0001g0039 a0005c0006t0001g0041 a0005c0006t0001g0268 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5749+3314A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710211 | |||||||
chr11:93710225 | G | T | 1 | a0001c0001t0001g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5749+3328G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710225 | |||||||
chr11:93710273 | A | G | 6 | a0005c0006t0001g0039 a0005c0006t0001g0041 a0005c0006t0001g0268 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5749+3376A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710273 | |||||||
chr11:93710372 | A | C | 1 | a0001c0001t0001g0056 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5749+3475A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710372 | |||||||
chr11:93710462 | C | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(95): Show |
117 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.5749+3565C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710462 | |||||||
chr11:93710526 | G | T | 1 | a0001c0001t0001g0259 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.5749+3629G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710526 | |||||||
chr11:93710616 | A | G | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+3719A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710616 | |||||||
chr11:93710642 | G | A | 1 | a0004c0043t0001g0122 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5749+3745G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710642 | |||||||
chr11:93710711 | G | A | 1 | a0004c0005t0001g0111 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5749+3814G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710711 | |||||||
chr11:93710730 | G | A | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+3833G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710730 | |||||||
chr11:93710750 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5749+3853T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710750 | |||||||
chr11:93710891 | T | C | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5749+3994T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710891 | |||||||
chr11:93710925 | C | A | 4 | a0003c0002t0001g0085 a0003c0002t0001g0086 a0003c0002t0001g0093 others(1): Show |
4 | NA18966.hp1 NA18979.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.5749+4028C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93710925 | |||||||
chr11:93710986 | CCTT | C | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+4093_5749+409 others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93710986 | ||||||
chr11:93711063 | T | A | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5749+4166T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711063 | |||||||
chr11:93711213 | T | C | 3 | a0002c0003t0001g0024 a0002c0003t0001g0290 a0002c0003t0001g0291 |
4 | HG02258.hp2 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5749+4316T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711213 | |||||||
chr11:93711392 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | HG00408.hp2 NA18945.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.5749+4495A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711392 | |||||||
chr11:93711481 | G | GTTTTGT | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.5749+4618_5749+462 others(10): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93711481 | ||||||
chr11:93711481 | GTTTTGT | G | 3 | a0001c0001t0001g0228 a0009c0017t0002g0304 a0009c0017t0002g0307 |
3 | HG01099.hp1 HG02056.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5749+4618_5749+462 others(10): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93711481 | ||||||
chr11:93711481 | GTTTTGTT others(11): Show |
G | 1 | a0001c0001t0001g0222 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5749+4606_5749+462 others(22): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93711481 | ||||||
chr11:93711518 | T | G | 1 | a0009c0017t0002g0304 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5749+4621T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711518 | |||||||
chr11:93711789 | G | C | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5749+4892G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711789 | |||||||
chr11:93711826 | GTT | G | 9 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0030 others(6): Show |
13 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.5749+4941_5749+494 others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93711826 | ||||||
chr11:93711829 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5749+4932T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711829 | |||||||
chr11:93711830 | T | G | 4 | a0002c0010t0001g0022 a0002c0010t0001g0286 a0009c0017t0002g0304 others(1): Show |
5 | HG01099.hp1 HG01884.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.5749+4933T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711830 | |||||||
chr11:93711834 | T | G | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5749+4937T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93711834 | |||||||
chr11:93712209 | C | CT | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+5322dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712209 | ||||||
chr11:93712209 | CT | C | 6 | a0005c0006t0001g0039 a0005c0006t0001g0041 a0005c0006t0001g0268 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.5749+5322delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712209 | ||||||
chr11:93712220 | C | T | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+5323C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712220 | |||||||
chr11:93712261 | T | A | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+5364T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712261 | |||||||
chr11:93712277 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.5749+5380C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712277 | |||||||
chr11:93712289 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5749+5392C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712289 | |||||||
chr11:93712679 | A | G | 1 | a0004c0005t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5749+5782A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712679 | |||||||
chr11:93712832 | T | C | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5749+5935T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93712832 | |||||||
chr11:93712856 | T | TTTG | 79 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(76): Show |
83 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.5749+5995_5749+599 others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | ||||||
chr11:93712856 | T | TTTGTTG | 17 | a0001c0001t0001g0017 a0001c0001t0001g0186 a0001c0001t0001g0206 others(14): Show |
18 | HG01109.hp2 HG01192.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.5749+5992_5749+599 others(10): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | ||||||
chr11:93712856 | T | TTTGTTGT others(2): Show |
5 | a0005c0006t0001g0041 a0005c0011t0001g0242 a0005c0011t0001g0244 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.5749+5989_5749+599 others(13): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | ||||||
chr11:93712856 | TTTG | T | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.5749+5995_5749+599 others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | ||||||
chr11:93712856 | TTTGTTG | T | 14 | a0001c0001t0001g0056 a0002c0003t0001g0280 a0003c0002t0001g0092 others(11): Show |
18 | HG02015.hp2 HG02165.hp1 HG02698.hp1 others(15): Show |
intron_variant | MODIFIER | c.5749+5992_5749+599 others(10): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | ||||||
chr11:93712856 | TTTGTTGT others(11): Show |
T | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5749+5980_5749+599 others(22): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93712856 | ||||||
chr11:93713211 | CTGTT | C | 11 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(8): Show |
15 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(12): Show |
intron_variant | MODIFIER | c.5749+6316_5749+631 others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93713211 | ||||||
chr11:93713228 | G | A | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5749+6331G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713228 | |||||||
chr11:93713491 | G | T | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+6594G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713491 | |||||||
chr11:93713492 | C | T | 1 | a0003c0002t0001g0086 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.5749+6595C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713492 | |||||||
chr11:93713533 | G | A | 1 | a0005c0006t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5749+6636G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713533 | |||||||
chr11:93713785 | G | A | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5749+6888G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713785 | |||||||
chr11:93713914 | A | ATTC | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+7019_5749+702 others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93713914 | ||||||
chr11:93713998 | T | A | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5749+7101T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93713998 | |||||||
chr11:93714022 | C | T | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5749+7125C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714022 | |||||||
chr11:93714161 | C | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.5750-7151C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714161 | |||||||
chr11:93714217 | T | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0209 |
2 | NA18945.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.5750-7095T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714217 | |||||||
chr11:93714247 | G | A | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5750-7065G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714247 | |||||||
chr11:93714275 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.5750-7037G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714275 | |||||||
chr11:93714291 | T | G | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-7021T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714291 | |||||||
chr11:93714376 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5750-6936A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714376 | |||||||
chr11:93714395 | C | T | 55 | a0003c0002t0001g0001 a0003c0002t0001g0006 a0003c0002t0001g0078 others(52): Show |
65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.5750-6917C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714395 | |||||||
chr11:93714407 | C | T | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-6905C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714407 | |||||||
chr11:93714570 | G | A | 1 | a0005c0033t0001g0038 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5750-6742G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714570 | |||||||
chr11:93714660 | T | G | 2 | a0002c0019t0001g0282 a0002c0019t0001g0283 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5750-6652T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714660 | |||||||
chr11:93714673 | C | G | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-6639C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714673 | |||||||
chr11:93714788 | G | A | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5750-6524G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714788 | |||||||
chr11:93714790 | A | T | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5750-6522A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714790 | |||||||
chr11:93714810 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.5750-6502T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714810 | |||||||
chr11:93714827 | A | G | 1 | a0006c0004t0001g0032 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.5750-6485A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93714827 | |||||||
chr11:93714842 | C | CCT | 65 | a0003c0002t0001g0001 a0003c0002t0001g0006 a0003c0002t0001g0078 others(62): Show |
79 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.5750-6451_5750-645 others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93714842 | ||||||
chr11:93715097 | C | T | 1 | a0009c0017t0002g0307 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5750-6215C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715097 | |||||||
chr11:93715140 | C | T | 1 | a0005c0006t0001g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5750-6172C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715140 | |||||||
chr11:93715193 | A | G | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5750-6119A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715193 | |||||||
chr11:93715302 | TG | T | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5750-6009delG | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715302 | |||||||
chr11:93715353 | G | T | 1 | a0006c0004t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.5750-5959G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715353 | |||||||
chr11:93715423 | A | G | 255 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.5750-5889A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715423 | |||||||
chr11:93715591 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5750-5721G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715591 | |||||||
chr11:93715654 | T | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.5750-5658T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715654 | |||||||
chr11:93715732 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5750-5580A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715732 | |||||||
chr11:93715760 | T | C | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-5552T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715760 | |||||||
chr11:93715843 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.5750-5469A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715843 | |||||||
chr11:93715896 | G | A | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5750-5416G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93715896 | |||||||
chr11:93716013 | C | T | 1 | a0001c0001t0001g0019 | 2 | NA18966.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.5750-5299C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716013 | |||||||
chr11:93716021 | G | A | 1 | a0002c0003t0001g0276 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5750-5291G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716021 | |||||||
chr11:93716187 | A | G | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5750-5125A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716187 | |||||||
chr11:93716233 | C | T | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-5079C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716233 | |||||||
chr11:93716287 | A | C | 12 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0053 others(9): Show |
12 | HG00140.hp2 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.5750-5025A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716287 | |||||||
chr11:93716457 | C | T | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5750-4855C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716457 | |||||||
chr11:93716471 | G | A | 1 | a0005c0006t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5750-4841G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716471 | |||||||
chr11:93716531 | T | C | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-4781T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716531 | |||||||
chr11:93716549 | G | A | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5750-4763G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716549 | |||||||
chr11:93716569 | C | T | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5750-4743C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716569 | |||||||
chr11:93716606 | C | T | 3 | a0004c0009t0001g0036 a0004c0009t0001g0037 a0004c0009t0001g0121 |
3 | HG03130.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5750-4706C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716606 | |||||||
chr11:93716652 | G | T | 8 | a0002c0003t0001g0021 a0002c0003t0001g0025 a0002c0003t0001g0275 others(5): Show |
10 | HG01081.hp1 HG02486.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.5750-4660G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716652 | |||||||
chr11:93716968 | A | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.5750-4344A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93716968 | |||||||
chr11:93717004 | C | T | 2 | a0005c0006t0001g0041 a0016c0028t0001g0040 |
2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.5750-4308C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717004 | |||||||
chr11:93717043 | A | C | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5750-4269A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717043 | |||||||
chr11:93717132 | C | T | 2 | a0005c0006t0001g0268 a0005c0006t0001g0269 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.5750-4180C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717132 | |||||||
chr11:93717162 | A | C | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5750-4150A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717162 | |||||||
chr11:93717168 | C | T | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5750-4144C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717168 | |||||||
chr11:93717212 | G | T | 1 | a0018c0038t0001g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5750-4100G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717212 | |||||||
chr11:93717386 | G | A | 1 | a0005c0006t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5750-3926G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717386 | |||||||
chr11:93717751 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5750-3561T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717751 | |||||||
chr11:93717780 | C | T | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-3532C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717780 | |||||||
chr11:93717904 | G | A | 6 | a0001c0001t0001g0216 a0001c0001t0001g0221 a0001c0001t0001g0222 others(3): Show |
6 | HG02622.hp1 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.5750-3408G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717904 | |||||||
chr11:93717911 | A | T | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-3401A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93717911 | |||||||
chr11:93718036 | C | T | 1 | a0002c0010t0001g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5750-3276C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718036 | |||||||
chr11:93718040 | T | G | 3 | a0008c0008t0001g0010 a0008c0008t0001g0082 a0008c0008t0001g0119 |
4 | HG02451.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5750-3272T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718040 | |||||||
chr11:93718092 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5750-3220G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718092 | |||||||
chr11:93718128 | C | A | 1 | a0001c0001t0001g0261 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5750-3184C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718128 | |||||||
chr11:93718172 | A | C | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-3140A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718172 | |||||||
chr11:93718181 | G | A | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5750-3131G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718181 | |||||||
chr11:93718198 | A | G | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-3114A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718198 | |||||||
chr11:93718249 | A | G | 1 | a0004c0005t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5750-3063A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718249 | |||||||
chr11:93718392 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5750-2920G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718392 | |||||||
chr11:93718465 | T | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0229 a0001c0001t0001g0230 others(7): Show |
11 | HG01109.hp2 HG01192.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.5750-2847T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718465 | |||||||
chr11:93718570 | C | T | 1 | a0003c0002t0001g0078 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.5750-2742C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93718570 | |||||||
chr11:93719105 | C | CA | 255 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.5750-2199dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93719105 | ||||||
chr11:93719221 | T | A | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.5750-2091T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719221 | |||||||
chr11:93719246 | G | GGT | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5750-2066_5750-206 others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719246 | |||||||
chr11:93719246 | G | GT | 37 | a0001c0001t0001g0175 a0002c0003t0001g0020 a0002c0003t0001g0021 others(34): Show |
43 | HG00673.hp1 HG01074.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.5750-2052dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93719246 | ||||||
chr11:93719246 | GT | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.5750-2052delT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93719246 | ||||||
chr11:93719247 | T | G | 1 | a0004c0005t0003g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5750-2065T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719247 | |||||||
chr11:93719349 | A | G | 1 | a0009c0017t0002g0304 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5750-1963A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719349 | |||||||
chr11:93719465 | G | C | 2 | a0001c0013t0001g0202 a0001c0013t0001g0205 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.5750-1847G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719465 | |||||||
chr11:93719605 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5750-1707C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719605 | |||||||
chr11:93719626 | A | G | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5750-1686A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719626 | |||||||
chr11:93719702 | T | G | 1 | a0002c0003t0001g0276 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5750-1610T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719702 | |||||||
chr11:93719928 | A | C | 255 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.5750-1384A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93719928 | |||||||
chr11:93720062 | T | TA | 290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.5750-1236dupA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720062 | ||||||
chr11:93720062 | TA | T | 12 | a0005c0033t0001g0038 a0006c0004t0001g0002 a0006c0004t0001g0027 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03041.hp2 others(13): Show |
intron_variant | MODIFIER | c.5750-1236delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720062 | ||||||
chr11:93720083 | C | T | 3 | a0005c0011t0001g0242 a0005c0011t0001g0244 a0014c0023t0001g0243 |
3 | HG01255.hp1 HG01891.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.5750-1229C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720083 | |||||||
chr11:93720114 | TCAGGAGG others(6): Show |
T | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-1190_5750-117 others(17): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720114 | ||||||
chr11:93720270 | C | T | 88 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(85): Show |
92 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.5750-1042C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720270 | |||||||
chr11:93720271 | G | A | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5750-1041G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720271 | |||||||
chr11:93720289 | A | G | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5750-1023A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720289 | |||||||
chr11:93720308 | A | G | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-1004A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720308 | |||||||
chr11:93720381 | G | C | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-931G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720381 | |||||||
chr11:93720450 | G | A | 1 | a0006c0004t0001g0029 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.5750-862G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720450 | |||||||
chr11:93720473 | CA | C | 17 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0025 others(14): Show |
20 | HG01081.hp1 HG01192.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.5750-822delA | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720473 | ||||||
chr11:93720489 | A | AAAAAAAG | 16 | a0001c0001t0001g0007 a0001c0001t0001g0126 a0001c0001t0001g0134 others(13): Show |
18 | HG00673.hp2 HG02055.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.5750-822_5750-821i others(9): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720489 | ||||||
chr11:93720489 | A | AAAAAAG | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.5750-822_5750-821i others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720489 | ||||||
chr11:93720489 | A | AAAAAG | 153 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
167 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.5750-822_5750-821i others(7): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720489 | ||||||
chr11:93720489 | A | AAAAG | 6 | a0001c0001t0001g0199 a0005c0014t0001g0076 a0005c0014t0001g0077 others(3): Show |
6 | HG02004.hp1 HG02280.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.5750-822_5750-821i others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720489 | ||||||
chr11:93720489 | A | AAAG | 9 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(6): Show |
13 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.5750-822_5750-821i others(5): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720489 | ||||||
chr11:93720589 | T | C | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-723T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720589 | |||||||
chr11:93720616 | G | A | 1 | a0005c0014t0001g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5750-696G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720616 | |||||||
chr11:93720785 | T | C | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5750-527T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720785 | |||||||
chr11:93720922 | T | C | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5750-390T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720922 | |||||||
chr11:93720926 | TGCATGTT others(3): Show |
T | 1 | a0002c0003t0001g0280 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5750-381_5750-372d others(12): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr11 | 93720926 | ||||||
chr11:93720981 | T | A | 1 | a0003c0002t0001g0090 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.5750-331T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 18/29 | chr11 | 93720981 | |||||||
chr11:93721453 | T | A | 1 | a0001c0001t0001g0236 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5850+41T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | chr11 | 93721453 | |||||||
chr11:93721477 | A | G | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5850+65A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | chr11 | 93721477 | |||||||
chr11:93721491 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.5850+79A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | chr11 | 93721491 | |||||||
chr11:93721665 | G | GGT | 81 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(78): Show |
89 | HG00323.hp2 HG00621.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.5851-254_5851-253d others(4): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | ||||||
chr11:93721665 | G | GGTGT | 12 | a0001c0001t0001g0068 a0001c0001t0001g0176 a0001c0001t0001g0181 others(9): Show |
12 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.5851-256_5851-253d others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | ||||||
chr11:93721665 | G | GGTGTGTG others(1): Show |
4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0209 others(1): Show |
4 | HG00408.hp2 HG02004.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.5851-260_5851-253d others(10): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | ||||||
chr11:93721665 | GGT | G | 70 | a0001c0001t0001g0018 a0001c0001t0001g0056 a0001c0001t0001g0123 others(67): Show |
83 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.5851-254_5851-253d others(4): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | ||||||
chr11:93721665 | GGTGT | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
131 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.5851-256_5851-253d others(6): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | ||||||
chr11:93721665 | GGTGTGT | G | 8 | a0001c0001t0001g0140 a0001c0001t0001g0156 a0001c0001t0001g0258 others(5): Show |
8 | HG00438.hp1 HG02080.hp1 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.5851-258_5851-253d others(8): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | ||||||
chr11:93721665 | GGTGTGTG others(3): Show |
G | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5851-262_5851-253d others(12): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721665 | ||||||
chr11:93721722 | A | AT | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.5851-231dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr11 | 93721722 | ||||||
chr11:93721726 | C | G | 1 | a0002c0010t0001g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5851-228C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 19/29 | chr11 | 93721726 | |||||||
chr11:93722089 | C | T | 5 | a0001c0001t0001g0063 a0001c0001t0001g0169 a0001c0001t0001g0171 others(2): Show |
5 | HG01358.hp2 HG01928.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.5947+39C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722089 | |||||||
chr11:93722248 | C | G | 3 | a0002c0003t0001g0024 a0002c0003t0001g0290 a0002c0003t0001g0291 |
4 | HG02258.hp2 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.5947+198C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722248 | |||||||
chr11:93722277 | G | A | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.5947+227G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722277 | |||||||
chr11:93722355 | A | G | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.5947+305A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722355 | |||||||
chr11:93722395 | A | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0213 |
2 | HG00323.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.5947+345A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722395 | |||||||
chr11:93722418 | C | T | 3 | a0005c0006t0001g0268 a0005c0006t0001g0269 a0005c0006t0001g0270 |
3 | HG02895.hp2 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5947+368C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722418 | |||||||
chr11:93722505 | C | T | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.5947+455C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722505 | |||||||
chr11:93722826 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
6 | HG00438.hp2 HG02080.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.5948-215C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722826 | |||||||
chr11:93722854 | G | A | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.5948-187G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722854 | |||||||
chr11:93722924 | G | A | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5948-117G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93722924 | |||||||
chr11:93723031 | C | G | 1 | a0001c0001t0001g0264 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.5948-10C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 20/29 | chr11 | 93723031 | |||||||
chr11:93723385 | A | G | 1 | a0005c0006t0001g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.6196+96A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723385 | |||||||
chr11:93723549 | G | A | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.6196+260G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723549 | |||||||
chr11:93723589 | C | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
121 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.6196+300C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723589 | |||||||
chr11:93723606 | C | T | 2 | a0003c0002t0001g0006 a0031c0044t0001g0080 |
4 | NA18747.hp1 NA18945.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.6196+317C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723606 | |||||||
chr11:93723910 | C | T | 1 | a0004c0005t0001g0111 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.6197-344C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723910 | |||||||
chr11:93723969 | A | T | 13 | a0002c0003t0001g0281 a0006c0004t0001g0002 a0006c0004t0001g0027 others(10): Show |
17 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(14): Show |
intron_variant | MODIFIER | c.6197-285A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723969 | |||||||
chr11:93723970 | T | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0200 |
2 | HG02738.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.6197-284T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93723970 | |||||||
chr11:93724150 | G | A | 2 | a0001c0001t0001g0160 a0033c0042t0001g0151 |
2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.6197-104G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93724150 | |||||||
chr11:93724150 | G | T | 1 | a0003c0002t0001g0094 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.6197-104G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93724150 | |||||||
chr11:93724163 | T | C | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6197-91T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93724163 | |||||||
chr11:93724239 | A | T | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6197-15A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 21/29 | chr11 | 93724239 | |||||||
chr11:93724536 | G | A | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.6318+161G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724536 | |||||||
chr11:93724598 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.6318+223C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724598 | |||||||
chr11:93724638 | G | A | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.6318+263G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724638 | |||||||
chr11:93724665 | G | T | 1 | a0001c0016t0001g0012 | 2 | NA19077.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.6318+290G>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724665 | |||||||
chr11:93724702 | G | A | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.6318+327G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724702 | |||||||
chr11:93724722 | G | A | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6318+347G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724722 | |||||||
chr11:93724853 | A | C | 4 | a0002c0003t0001g0020 a0002c0003t0001g0274 a0002c0003t0001g0277 others(1): Show |
5 | HG01243.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.6318+478A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724853 | |||||||
chr11:93724876 | T | C | 1 | a0004c0005t0001g0098 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.6318+501T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724876 | |||||||
chr11:93724886 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6318+511T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724886 | |||||||
chr11:93724970 | T | C | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.6318+595T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724970 | |||||||
chr11:93724992 | T | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.6318+617T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93724992 | |||||||
chr11:93725026 | A | G | 305 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(302): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.6319-625A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725026 | |||||||
chr11:93725114 | G | C | 1 | a0005c0006t0001g0042 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6319-537G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725114 | |||||||
chr11:93725147 | G | A | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.6319-504G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725147 | |||||||
chr11:93725201 | C | T | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(250): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.6319-450C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725201 | |||||||
chr11:93725587 | G | A | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.6319-64G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725587 | |||||||
chr11:93725612 | T | C | 1 | a0002c0010t0001g0022 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6319-39T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 22/29 | chr11 | 93725612 | |||||||
chr11:93725865 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.6499+34T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93725865 | |||||||
chr11:93726053 | TTCCCTAC others(7): Show |
T | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6499+223_6499+236d others(16): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726053 | |||||||
chr11:93726071 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6499+240A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726071 | |||||||
chr11:93726097 | A | C | 305 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(302): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.6499+266A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726097 | |||||||
chr11:93726225 | G | A | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6499+394G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726225 | |||||||
chr11:93726342 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.6499+511C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726342 | |||||||
chr11:93726361 | C | G | 256 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(253): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.6499+530C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726361 | |||||||
chr11:93726472 | C | T | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.6500-504C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | chr11 | 93726472 | |||||||
chr11:93726738 | TATAGCCA others(25): Show |
T | 1 | a0027c0039t0001g0301 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.6500-236_6500-205d others(34): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr11 | 93726738 | ||||||
chr11:93727695 | T | C | 4 | a0002c0003t0001g0025 a0002c0003t0001g0302 a0002c0003t0001g0303 others(1): Show |
5 | NA18953.hp1 NA18968.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.7161+58T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93727695 | |||||||
chr11:93727728 | A | G | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.7161+91A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93727728 | |||||||
chr11:93727731 | C | T | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.7161+94C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93727731 | |||||||
chr11:93727770 | C | T | 1 | a0026c0030t0001g0211 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7161+133C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93727770 | |||||||
chr11:93727895 | A | G | 6 | a0005c0006t0001g0039 a0005c0006t0001g0041 a0005c0006t0001g0268 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.7161+258A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93727895 | |||||||
chr11:93728015 | T | A | 2 | a0011c0018t0001g0305 a0011c0018t0001g0306 |
2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.7161+378T>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728015 | |||||||
chr11:93728056 | A | G | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7161+419A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728056 | |||||||
chr11:93728196 | A | C | 1 | a0001c0001t0001g0271 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.7162-485A>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728196 | |||||||
chr11:93728235 | G | A | 256 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(253): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.7162-446G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728235 | |||||||
chr11:93728274 | C | G | 1 | a0004c0005t0001g0101 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.7162-407C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728274 | |||||||
chr11:93728329 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7162-352C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728329 | |||||||
chr11:93728434 | C | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0248 |
2 | HG00621.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.7162-247C>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728434 | |||||||
chr11:93728555 | T | C | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.7162-126T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728555 | |||||||
chr11:93728674 | T | G | 1 | a0027c0039t0001g0301 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.7162-7T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728674 | |||||||
chr11:93728675 | T | G | 1 | a0027c0039t0001g0301 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.7162-6T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728675 | |||||||
chr11:93728676 | C | G | 1 | a0027c0039t0001g0301 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.7162-5C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728676 | |||||||
chr11:93728677 | A | G | 1 | a0027c0039t0001g0301 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.7162-4A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728677 | |||||||
chr11:93728678 | C | G | 1 | a0027c0039t0001g0301 | 1 | NA18986.hp2 | splice_region_variant&intron_variant | LOW | c.7162-3C>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728678 | |||||||
chr11:93728679 | A | G | 1 | a0027c0039t0001g0301 | 1 | NA18986.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.7162-2A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 24/29 | chr11 | 93728679 | |||||||
chr11:93728891 | T | G | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.7302+70T>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93728891 | |||||||
chr11:93728936 | G | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.7302+115G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93728936 | |||||||
chr11:93729039 | G | C | 2 | a0005c0014t0001g0076 a0005c0014t0001g0077 |
2 | HG02004.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.7302+218G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729039 | |||||||
chr11:93729159 | A | G | 1 | a0009c0017t0002g0307 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.7303-275A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729159 | |||||||
chr11:93729359 | C | T | 1 | a0005c0006t0001g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.7303-75C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729359 | |||||||
chr11:93729385 | C | T | 2 | a0009c0017t0002g0304 a0009c0017t0002g0307 |
2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7303-49C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729385 | |||||||
chr11:93729394 | C | T | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.7303-40C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729394 | |||||||
chr11:93729403 | A | AGAGTT | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.7303-27_7303-26ins others(5): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr11 | 93729403 | ||||||
chr11:93729414 | T | C | 1 | a0002c0010t0001g0022 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.7303-20T>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729414 | |||||||
chr11:93729415 | G | C | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
intron_variant | MODIFIER | c.7303-19G>C | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | chr11 | 93729415 | |||||||
chr11:93729419 | C | CT | 10 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(7): Show |
14 | HG02165.hp1 NA18940.hp2 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.7303-12dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr11 | 93729419 | ||||||
chr11:93729553 | A | T | 1 | a0005c0026t0001g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7399+23A>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 26/29 | chr11 | 93729553 | |||||||
chr11:93729603 | T | TC | 12 | a0006c0004t0001g0002 a0006c0004t0001g0027 a0006c0004t0001g0029 others(9): Show |
16 | HG01099.hp1 HG02165.hp1 HG03579.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.7400-6dupC | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr11 | 93729603 | ||||||
chr11:93729975 | GTTAA | G | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.7667+9_7667+12delA others(3): Show |
CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr11 | 93729975 | ||||||
chr11:93729979 | A | AT | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
129 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.7667+26dupT | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr11 | 93729979 | ||||||
chr11:93730151 | G | A | 1 | a0005c0006t0001g0061 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.7767+3G>A | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 29/29 | chr11 | 93730151 | |||||||
chr11:93730166 | A | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.7767+18A>G | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 29/29 | chr11 | 93730166 | |||||||
chr11:93730221 | C | T | 1 | a0005c0006t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7768-10C>T | CEP295 | ENSG00000166004.15 | transcript | ENST00000325212.11 | protein_coding | 29/29 | chr11 | 93730221 |