Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8881 |
| ensemblid | ENSG00000130177.16 |
| hgncid | 1720 |
| symbol | CDC16 |
| name | cell division cycle 16 |
| refseq_nuc | NM_001078645.3 |
| refseq_prot | NP_001072113.1 |
| ensembl_nuc | ENST00000356221.8 |
| ensembl_prot | ENSP00000348554.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 114234897 |
| end | 114272723 |
| strand | + |
| ver | v1.2 |
| region | chr13:114234897-114272723 |
| region5000 | chr13:114229897-114277723 |
| regionname0 | CDC16_chr13_114234897_114272723 |
| regionname5000 | CDC16_chr13_114229897_114277723 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1860 | 206 | 14 | 36 | 119 | 16 | 19 | CDC16_chr13_114229897_114277723 | CDC16 | ATGAA others(1855): Show |
chr13 | 114229897 | 114277723 | ||
| a0001c0002 | 0/0 | 1860 | 121 | 49 | 20 | 32 | 0 | 20 | CDC16_chr13_114229897_114277723 | CDC16 | ATGAA others(1855): Show |
chr13 | 114229897 | 114277723 | ||
| a0001c0003 | 0/0 | 1860 | 23 | 12 | 6 | 5 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | ATGAA others(1855): Show |
chr13 | 114229897 | 114277723 | ||
| a0001c0004 | 0/0 | 1860 | 14 | 0 | 7 | 6 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | ATGAA others(1855): Show |
chr13 | 114229897 | 114277723 | ||
| a0001c0005 | 0/0 | 1860 | 12 | 9 | 3 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | ATGAA others(1855): Show |
chr13 | 114229897 | 114277723 | ||
| a0001c0006 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | ATGAA others(1855): Show |
chr13 | 114229897 | 114277723 | ||
| a0001c0007 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | ATGAA others(1855): Show |
chr13 | 114229897 | 114277723 | ||
| a0001c0008 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | ATGAA others(1855): Show |
chr13 | 114229897 | 114277723 | ||
| a0001c0009 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | ATGAA others(1855): Show |
chr13 | 114229897 | 114277723 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2331 | 203 | 13 | 36 | 118 | 16 | 18 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2326): Show |
chr13 | 114229897 | 114277723 |
| a0001c0001t0013 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2326): Show |
chr13 | 114229897 | 114277723 |
| a0001c0001t0014 | 0/0 | 2331 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2326): Show |
chr13 | 114229897 | 114277723 |
| a0001c0001t0016 | 0/0 | 2316 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2311): Show |
chr13 | 114229897 | 114277723 |
| a0001c0002t0002 | 0/0 | 2337 | 109 | 40 | 17 | 32 | 0 | 20 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2332): Show |
chr13 | 114229897 | 114277723 |
| a0001c0002t0007 | 0/0 | 2343 | 4 | 4 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2338): Show |
chr13 | 114229897 | 114277723 |
| a0001c0002t0008 | 0/0 | 2343 | 3 | 3 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2338): Show |
chr13 | 114229897 | 114277723 |
| a0001c0002t0009 | 0/0 | 2331 | 2 | 0 | 2 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2326): Show |
chr13 | 114229897 | 114277723 |
| a0001c0002t0011 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2326): Show |
chr13 | 114229897 | 114277723 |
| a0001c0002t0012 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2338): Show |
chr13 | 114229897 | 114277723 |
| a0001c0002t0015 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2332): Show |
chr13 | 114229897 | 114277723 |
| a0001c0003t0001 | 0/0 | 2331 | 13 | 5 | 3 | 5 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2326): Show |
chr13 | 114229897 | 114277723 |
| a0001c0003t0002 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2332): Show |
chr13 | 114229897 | 114277723 |
| a0001c0003t0004 | 0/0 | 2331 | 8 | 5 | 3 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2326): Show |
chr13 | 114229897 | 114277723 |
| a0001c0004t0003 | 0/0 | 2331 | 14 | 0 | 7 | 6 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2326): Show |
chr13 | 114229897 | 114277723 |
| a0001c0005t0005 | 0/0 | 2337 | 6 | 4 | 2 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2332): Show |
chr13 | 114229897 | 114277723 |
| a0001c0005t0006 | 0/0 | 2337 | 6 | 5 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2332): Show |
chr13 | 114229897 | 114277723 |
| a0001c0006t0010 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2332): Show |
chr13 | 114229897 | 114277723 |
| a0001c0007t0002 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2332): Show |
chr13 | 114229897 | 114277723 |
| a0001c0008t0002 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2332): Show |
chr13 | 114229897 | 114277723 |
| a0001c0009t0001 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | AGTGC others(2326): Show |
chr13 | 114229897 | 114277723 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 24 | 3 | 6 | 11 | 2 | 2 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0002 | 0/0 | 20 | 0 | 0 | 16 | 0 | 4 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0003 | 0/0 | 13 | 0 | 0 | 11 | 0 | 2 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0013g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0014g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0001t0016g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0004 | 0/0 | 11 | 0 | 0 | 9 | 0 | 2 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0009 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0017 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0043 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0007g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0008g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0009g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0002t0015g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0001g0022 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0004g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0003t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0004t0003g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0004t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0004t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0004t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0004t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0004t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0004t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0004t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0004t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0005t0005g0005 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0005t0006g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0005t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0005t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0005t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0006t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0007t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0008t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| a0001c0009t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0180 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0189 | EAS | CHS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0208 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00642 | hp1 | a0001 | c0004 | t0003 | g0030 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0195 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00735 | hp2 | a0001 | c0003 | t0004 | g0021 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00738 | hp2 | a0001 | c0002 | t0015 | g0200 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01069 | hp1 | a0001 | c0005 | t0005 | g0005 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01070 | hp1 | a0001 | c0003 | t0004 | g0021 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0206 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01071 | hp1 | a0001 | c0003 | t0004 | g0021 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01071 | hp2 | a0001 | c0005 | t0005 | g0005 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0182 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01167 | hp2 | a0001 | c0002 | t0009 | g0024 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0204 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01169 | hp2 | a0001 | c0002 | t0009 | g0024 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0017 | AMR | PUR | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0197 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0017 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0199 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01361 | hp1 | a0001 | c0004 | t0003 | g0030 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01496 | hp2 | a0001 | c0005 | t0006 | g0020 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01993 | hp1 | a0001 | c0004 | t0003 | g0070 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01993 | hp2 | a0001 | c0004 | t0003 | g0073 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02004 | hp2 | a0001 | c0004 | t0003 | g0052 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02040 | hp1 | a0001 | c0004 | t0003 | g0071 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02257 | hp1 | a0001 | c0005 | t0006 | g0077 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0194 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02258 | hp1 | a0001 | c0005 | t0005 | g0005 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02258 | hp2 | a0001 | c0002 | t0008 | g0019 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02273 | hp1 | a0001 | c0004 | t0003 | g0072 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02273 | hp2 | a0001 | c0004 | t0003 | g0068 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02280 | hp1 | a0001 | c0005 | t0005 | g0005 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0178 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0179 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0060 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02615 | hp1 | a0001 | c0002 | t0012 | g0215 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0045 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02647 | hp1 | a0001 | c0002 | t0007 | g0048 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0057 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0192 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0181 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02818 | hp1 | a0001 | c0003 | t0004 | g0147 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0184 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02886 | hp1 | a0001 | c0003 | t0004 | g0146 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02895 | hp1 | a0001 | c0003 | t0004 | g0144 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0216 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0045 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0198 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02922 | hp2 | a0001 | c0005 | t0006 | g0020 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02970 | hp1 | a0001 | c0005 | t0006 | g0078 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02976 | hp2 | a0001 | c0006 | t0010 | g0211 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0064 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03098 | hp1 | a0001 | c0002 | t0007 | g0214 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03130 | hp1 | a0001 | c0003 | t0004 | g0148 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0185 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03139 | hp2 | a0001 | c0002 | t0008 | g0019 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0183 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0201 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03209 | hp1 | a0001 | c0002 | t0007 | g0213 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03225 | hp2 | a0001 | c0009 | t0001 | g0174 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0209 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0203 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0032 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0017 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03516 | hp1 | a0001 | c0005 | t0005 | g0005 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | ESN | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03579 | hp1 | a0001 | c0002 | t0008 | g0019 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0219 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03654 | hp1 | a0001 | c0001 | t0014 | g0115 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0202 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0075 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | BEB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03834 | hp2 | a0001 | c0004 | t0003 | g0069 | SAS | BEB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0031 | SAS | BEB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | STU | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0031 | SAS | STU | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0032 | SAS | BEB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0043 | SAS | BEB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | STU | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0017 | SAS | STU | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0067 | SAS | STU | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0207 | SAS | STU | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0212 | AFR | YRI | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0193 | AFR | YRI | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18906 | hp1 | a0001 | c0007 | t0002 | g0223 | AFR | YRI | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | YRI | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18954 | hp1 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0188 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18991 | hp1 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18999 | hp2 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0221 | AFR | LWK | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19030 | hp2 | a0001 | c0003 | t0004 | g0145 | AFR | LWK | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19043 | hp1 | a0001 | c0005 | t0006 | g0079 | AFR | LWK | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0217 | AFR | LWK | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19056 | hp1 | a0001 | c0001 | t0013 | g0014 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19074 | hp1 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19086 | hp1 | a0001 | c0004 | t0003 | g0010 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | YRI | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | ASW | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA20129 | hp2 | a0001 | c0002 | t0007 | g0048 | AFR | ASW | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | GIH | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | GIH | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02109 | hp1 | a0001 | c0001 | t0016 | g0002 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02109 | hp2 | a0001 | c0005 | t0006 | g0020 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0043 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG02559 | hp2 | a0001 | c0005 | t0005 | g0005 | AFR | ACB | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0196 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | USA | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA20300 | hp2 | a0001 | c0008 | t0002 | g0218 | AFR | USA | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | LWK | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| NA21309 | hp2 | a0001 | c0002 | t0011 | g0076 | AFR | LWK | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0087 | REF | REF | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0097 | REF | REF | CDC16_chr13_114229897_114277723 | CDC16 | chr13 | 114229897 | 114277723 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:114236830 | G | A | 5 | a0001c0002 a0001c0004 a0001c0006 others(2): Show |
138 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(135): Show |
synonymous_variant | LOW | c.135G>A | p.Gln45Gln | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/18 | 323/2331 | 135/1863 | 45/620 | chr13 | 114236830 | |||
| chr13:114236875 | T | A | 1 | a0001c0006 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.180T>A | p.Leu60Leu | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/18 | 368/2331 | 180/1863 | 60/620 | chr13 | 114236875 | |||
| chr13:114239439 | C | T | 8 | a0001c0002 a0001c0003 a0001c0004 others(5): Show |
174 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(171): Show |
synonymous_variant | LOW | c.330C>T | p.Asp110Asp | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/18 | 518/2331 | 330/1863 | 110/620 | chr13 | 114239439 | |||
| chr13:114239460 | T | C | 7 | a0001c0002 a0001c0003 a0001c0004 others(4): Show |
173 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(170): Show |
synonymous_variant | LOW | c.351T>C | p.Pro117Pro | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/18 | 539/2331 | 351/1863 | 117/620 | chr13 | 114239460 | |||
| chr13:114242135 | C | T | 1 | a0001c0005 | 12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
synonymous_variant | LOW | c.396C>T | p.Ile132Ile | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 6/18 | 584/2331 | 396/1863 | 132/620 | chr13 | 114242135 | |||
| chr13:114243909 | G | A | 1 | a0001c0004 | 14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
synonymous_variant | LOW | c.687G>A | p.Glu229Glu | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/18 | 875/2331 | 687/1863 | 229/620 | chr13 | 114243909 | |||
| chr13:114250561 | A | G | 1 | a0001c0008 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.984A>G | p.Thr328Thr | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/18 | 1172/2331 | 984/1863 | 328/620 | chr13 | 114250561 | |||
| chr13:114259335 | A | G | 1 | a0001c0007 | 1 | NA18906.hp1 | splice_region_variant&synonymous_variant | LOW | c.1251A>G | p.Glu417Glu | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/18 | 1439/2331 | 1251/1863 | 417/620 | chr13 | 114259335 | |||
| chr13:114265239 | T | C | 6 | a0001c0002 a0001c0004 a0001c0005 others(3): Show |
150 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(147): Show |
splice_region_variant&synonymous_variant | LOW | c.1602T>C | p.Ile534Ile | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/18 | 1790/2331 | 1602/1863 | 534/620 | chr13 | 114265239 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:114234905 | G | A | 1 | a0001c0002t0008 | 3 | HG02258.hp2 HG03139.hp2 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-180G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 180 | chr13 | 114234905 | ||||||
| chr13:114234907 | G | A | 1 | a0001c0004t0003 | 14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-178G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 178 | chr13 | 114234907 | ||||||
| chr13:114234908 | C | A | 2 | a0001c0005t0005 a0001c0005t0006 |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-177C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 177 | chr13 | 114234908 | ||||||
| chr13:114234909 | C | G | 1 | a0001c0002t0009 | 2 | HG01167.hp2 HG01169.hp2 |
5_prime_UTR_variant | MODIFIER | c.-176C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 176 | chr13 | 114234909 | ||||||
| chr13:114234938 | A | G | 4 | a0001c0002t0009 a0001c0004t0003 a0001c0005t0005 others(1): Show |
28 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-147A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 147 | chr13 | 114234938 | ||||||
| chr13:114234941 | TGCGGCCT others(8): Show |
T | 1 | a0001c0001t0016 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-128_-114delGCGGCC others(9): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 114 | INFO_REALIGN_3_PRIME | chr13 | 114234941 | |||||
| chr13:114234965 | C | G | 1 | a0001c0002t0015 | 1 | HG00738.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-120C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | chr13 | 114234965 | |||||||
| chr13:114234974 | G | GGGCGGC | 7 | a0001c0002t0002 a0001c0002t0007 a0001c0002t0008 others(4): Show |
120 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(117): Show |
5_prime_UTR_variant | MODIFIER | c.-101_-96dupGGCGGC | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 95 | INFO_REALIGN_3_PRIME | chr13 | 114234974 | |||||
| chr13:114234974 | G | GGGCGGCG others(5): Show |
1 | a0001c0002t0012 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107_-96dupGGCGGCG others(5): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 95 | INFO_REALIGN_3_PRIME | chr13 | 114234974 | |||||
| chr13:114234987 | G | A | 1 | a0001c0005t0005 | 6 | HG01069.hp1 HG01071.hp2 HG02258.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-98G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 98 | chr13 | 114234987 | ||||||
| chr13:114234990 | T | C | 14 | a0001c0002t0002 a0001c0002t0007 a0001c0002t0008 others(11): Show |
151 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(148): Show |
5_prime_UTR_variant | MODIFIER | c.-95T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 95 | chr13 | 114234990 | ||||||
| chr13:114234990 | T | G | 1 | a0001c0002t0007 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 95 | chr13 | 114234990 | ||||||
| chr13:114234991 | G | GCGGCCGC others(5): Show |
1 | a0001c0002t0007 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-93_-92insGGCCGCAG others(4): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 92 | INFO_REALIGN_3_PRIME | chr13 | 114234991 | |||||
| chr13:114234993 | A | AGGCACG | 5 | a0001c0002t0007 a0001c0002t0008 a0001c0005t0005 others(2): Show |
19 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-77_-72dupCACGGG | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 71 | INFO_REALIGN_3_PRIME | chr13 | 114234993 | |||||
| chr13:114234993 | A | G | 1 | a0001c0002t0007 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-92A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 92 | chr13 | 114234993 | ||||||
| chr13:114235020 | T | C | 2 | a0001c0005t0005 a0001c0005t0006 |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-65T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 65 | chr13 | 114235020 | ||||||
| chr13:114235032 | A | C | 2 | a0001c0005t0005 a0001c0005t0006 |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-53A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/18 | 53 | chr13 | 114235032 | ||||||
| chr13:114272534 | C | T | 1 | a0001c0003t0004 | 8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*91C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 18/18 | 91 | chr13 | 114272534 | ||||||
| chr13:114272605 | C | G | 1 | a0001c0001t0014 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 18/18 | 162 | chr13 | 114272605 | ||||||
| chr13:114272637 | A | G | 1 | a0001c0002t0011 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*194A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 18/18 | 194 | chr13 | 114272637 | ||||||
| chr13:114272638 | A | C | 1 | a0001c0001t0013 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*195A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 18/18 | 195 | chr13 | 114272638 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:114235175 | G | T | 45 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0013 others(42): Show |
72 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.48+43G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114235175 | |||||||
| chr13:114235244 | G | A | 89 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(86): Show |
150 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(147): Show |
intron_variant | MODIFIER | c.48+112G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114235244 | |||||||
| chr13:114235417 | A | G | 1 | a0001c0007t0002g0223 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.48+285A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114235417 | |||||||
| chr13:114235467 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.48+335A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114235467 | |||||||
| chr13:114235483 | A | C | 1 | a0001c0001t0001g0190 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.48+351A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114235483 | |||||||
| chr13:114235514 | C | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.48+382C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114235514 | |||||||
| chr13:114235584 | G | A | 1 | a0001c0002t0002g0192 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.48+452G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114235584 | |||||||
| chr13:114235758 | C | CAT | 3 | a0001c0003t0001g0042 a0001c0003t0001g0188 a0001c0003t0001g0189 |
4 | HG00621.hp2 NA18977.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+627_48+628insTA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 114235758 | ||||||
| chr13:114235818 | G | GCTGTGTT others(319): Show |
1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.48+700_48+701insTT others(324): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 114235818 | ||||||
| chr13:114235856 | G | A | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.48+724G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114235856 | |||||||
| chr13:114235883 | G | A | 2 | a0001c0002t0002g0193 a0001c0002t0002g0194 |
2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.48+751G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114235883 | |||||||
| chr13:114235944 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.49-701A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114235944 | |||||||
| chr13:114235996 | C | T | 1 | a0001c0002t0002g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.49-649C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114235996 | |||||||
| chr13:114236039 | CTG | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.49-605_49-604delTG | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236039 | |||||||
| chr13:114236084 | A | G | 1 | a0001c0002t0002g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.49-561A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236084 | |||||||
| chr13:114236094 | G | A | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.49-551G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236094 | |||||||
| chr13:114236259 | A | C | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.49-386A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236259 | |||||||
| chr13:114236422 | A | T | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.49-223A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236422 | |||||||
| chr13:114236456 | G | A | 1 | a0001c0002t0002g0051 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.49-189G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236456 | |||||||
| chr13:114236465 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.49-180C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236465 | |||||||
| chr13:114236481 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.49-164G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236481 | |||||||
| chr13:114236525 | A | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.49-120A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236525 | |||||||
| chr13:114236537 | A | G | 1 | a0001c0003t0002g0185 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.49-108A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236537 | |||||||
| chr13:114236572 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.49-73T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236572 | |||||||
| chr13:114236622 | C | CT | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.49-10dupT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr13 | 114236622 | ||||||
| chr13:114236638 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp1 | splice_region_variant&intron_variant | LOW | c.49-7T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 1/17 | chr13 | 114236638 | |||||||
| chr13:114236957 | C | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+61C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114236957 | |||||||
| chr13:114237042 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.201+146T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237042 | |||||||
| chr13:114237043 | G | A | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+147G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237043 | |||||||
| chr13:114237059 | C | T | 12 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0178 others(9): Show |
15 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.201+163C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237059 | |||||||
| chr13:114237098 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.201+202G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237098 | |||||||
| chr13:114237117 | C | T | 1 | a0001c0002t0008g0019 | 3 | HG02258.hp2 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.201+221C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237117 | |||||||
| chr13:114237208 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.201+312G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237208 | |||||||
| chr13:114237222 | C | CAA | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+338_201+339dup others(2): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114237222 | ||||||
| chr13:114237222 | CA | C | 5 | a0001c0002t0002g0018 a0001c0002t0002g0031 a0001c0002t0002g0032 others(2): Show |
9 | HG03491.hp2 HG03704.hp1 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.201+339delA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114237222 | ||||||
| chr13:114237284 | C | A | 89 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(86): Show |
150 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(147): Show |
intron_variant | MODIFIER | c.201+388C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237284 | |||||||
| chr13:114237356 | C | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+460C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237356 | |||||||
| chr13:114237425 | G | T | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.201+529G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237425 | |||||||
| chr13:114237432 | G | A | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+536G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237432 | |||||||
| chr13:114237449 | C | T | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.201+553C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237449 | |||||||
| chr13:114237483 | A | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+587A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237483 | |||||||
| chr13:114237506 | A | G | 3 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 |
3 | HG01109.hp1 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.201+610A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237506 | |||||||
| chr13:114237594 | G | GT | 18 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0192 others(15): Show |
28 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.201+707dupT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114237594 | ||||||
| chr13:114237602 | T | G | 1 | a0001c0003t0001g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.201+706T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237602 | |||||||
| chr13:114237653 | T | C | 1 | a0001c0002t0002g0074 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.201+757T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237653 | |||||||
| chr13:114237739 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.201+843C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237739 | |||||||
| chr13:114237879 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.201+983T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237879 | |||||||
| chr13:114237901 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.201+1005T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237901 | |||||||
| chr13:114237944 | A | G | 1 | a0001c0002t0002g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.202-1046A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237944 | |||||||
| chr13:114237946 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG00140.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.202-1044G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237946 | |||||||
| chr13:114237993 | C | G | 88 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(85): Show |
149 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.202-997C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114237993 | |||||||
| chr13:114238030 | C | T | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.202-960C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238030 | |||||||
| chr13:114238031 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0088 others(3): Show |
12 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.202-959G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238031 | |||||||
| chr13:114238044 | G | T | 2 | a0001c0002t0002g0050 a0001c0007t0002g0223 |
3 | HG02572.hp2 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.202-946G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238044 | |||||||
| chr13:114238047 | GTGC | G | 7 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0178 others(4): Show |
10 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.202-937_202-935del others(3): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238047 | ||||||
| chr13:114238065 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-925T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238065 | |||||||
| chr13:114238070 | A | ACCCAGCA others(164): Show |
5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-905_202-904ins others(171): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238070 | ||||||
| chr13:114238070 | ACCCAGCA others(50): Show |
A | 1 | a0001c0001t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.202-897_202-841del others(57): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238070 | ||||||
| chr13:114238090 | C | CAGGGCCT others(107): Show |
3 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 |
3 | HG01109.hp1 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.202-875_202-874ins others(114): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238090 | ||||||
| chr13:114238090 | CAGGGCCT others(107): Show |
C | 2 | a0001c0002t0002g0195 a0001c0002t0002g0196 |
2 | HG00733.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.202-868_202-755del | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238090 | ||||||
| chr13:114238093 | G | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-897G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238093 | |||||||
| chr13:114238113 | C | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-877C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238113 | |||||||
| chr13:114238116 | T | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-874T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238116 | |||||||
| chr13:114238122 | T | TGGACGCC others(107): Show |
39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(36): Show |
73 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.202-786_202-673dup others(114): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238122 | ||||||
| chr13:114238179 | C | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-811C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238179 | |||||||
| chr13:114238184 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-806G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238184 | |||||||
| chr13:114238204 | G | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-786G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238204 | |||||||
| chr13:114238204 | G | GAGGGCCT others(107): Show |
1 | a0001c0001t0001g0093 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.202-750_202-637dup others(114): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238204 | ||||||
| chr13:114238204 | G | GAGGGCCT others(563): Show |
1 | a0001c0001t0001g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.202-422_202-421ins others(570): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238204 | ||||||
| chr13:114238234 | C | A | 1 | a0001c0004t0003g0052 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.202-756C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238234 | |||||||
| chr13:114238236 | C | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-754C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238236 | |||||||
| chr13:114238284 | T | C | 1 | a0001c0002t0002g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.202-706T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238284 | |||||||
| chr13:114238289 | T | C | 27 | a0001c0002t0002g0004 a0001c0002t0002g0018 a0001c0002t0002g0025 others(24): Show |
46 | HG00735.hp1 HG00738.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.202-701T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238289 | |||||||
| chr13:114238293 | C | T | 4 | a0001c0002t0002g0018 a0001c0002t0002g0031 a0001c0002t0002g0032 others(1): Show |
8 | HG03491.hp2 HG03704.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-697C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238293 | |||||||
| chr13:114238297 | C | T | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.202-693C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238297 | |||||||
| chr13:114238321 | G | T | 11 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(8): Show |
20 | HG00735.hp2 HG01069.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.202-669G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238321 | |||||||
| chr13:114238354 | T | C | 12 | a0001c0001t0001g0035 a0001c0001t0001g0092 a0001c0001t0001g0149 others(9): Show |
21 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.202-636T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238354 | |||||||
| chr13:114238375 | C | G | 1 | a0001c0002t0002g0047 | 2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.202-615C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238375 | |||||||
| chr13:114238401 | G | GCTCCTCG others(50): Show |
5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-556_202-555ins others(57): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238401 | ||||||
| chr13:114238435 | G | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-555G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238435 | |||||||
| chr13:114238435 | GGCCTGAA others(107): Show |
G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.202-532_202-419del | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238435 | ||||||
| chr13:114238458 | G | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.202-532G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238458 | |||||||
| chr13:114238465 | G | GGACGCCC others(50): Show |
1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.202-476_202-475ins others(57): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238465 | ||||||
| chr13:114238492 | G | T | 14 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(11): Show |
26 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.202-498G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238492 | |||||||
| chr13:114238569 | C | T | 46 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0013 others(43): Show |
75 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.202-421C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238569 | |||||||
| chr13:114238570 | G | A | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.202-420G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238570 | |||||||
| chr13:114238728 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.202-262G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | chr13 | 114238728 | |||||||
| chr13:114238884 | AAGG | A | 1 | a0001c0002t0008g0019 | 3 | HG02258.hp2 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.202-103_202-101del others(3): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr13 | 114238884 | ||||||
| chr13:114239049 | AT | A | 73 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(70): Show |
121 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.240+26delT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr13 | 114239049 | ||||||
| chr13:114239080 | TGCATCTC others(14): Show |
T | 73 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(70): Show |
121 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.240+54_240+74delCA others(19): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr13 | 114239080 | ||||||
| chr13:114239091 | A | T | 16 | a0001c0002t0009g0024 a0001c0002t0011g0076 a0001c0004t0003g0010 others(13): Show |
29 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.240+63A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 4/17 | chr13 | 114239091 | |||||||
| chr13:114239169 | A | G | 1 | a0001c0003t0001g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.240+141A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 4/17 | chr13 | 114239169 | |||||||
| chr13:114239202 | C | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.241-148C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 4/17 | chr13 | 114239202 | |||||||
| chr13:114239327 | C | T | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.241-23C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 4/17 | chr13 | 114239327 | |||||||
| chr13:114239545 | C | T | 3 | a0001c0005t0006g0020 a0001c0005t0006g0078 a0001c0005t0006g0079 |
5 | HG01496.hp2 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+55C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114239545 | |||||||
| chr13:114239584 | A | G | 1 | a0001c0002t0002g0032 | 2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.381+94A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114239584 | |||||||
| chr13:114239606 | A | G | 1 | a0001c0002t0002g0029 | 2 | NA18942.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.381+116A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114239606 | |||||||
| chr13:114239608 | T | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.381+118T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114239608 | |||||||
| chr13:114239662 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(144): Show |
247 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.381+172T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114239662 | |||||||
| chr13:114239668 | C | A | 1 | a0001c0001t0001g0094 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.381+178C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114239668 | |||||||
| chr13:114239757 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.381+267A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114239757 | |||||||
| chr13:114239838 | T | C | 1 | a0001c0004t0003g0068 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.381+348T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114239838 | |||||||
| chr13:114239901 | T | C | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.381+411T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114239901 | |||||||
| chr13:114239942 | C | T | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.381+452C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114239942 | |||||||
| chr13:114240011 | T | TAA | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.381+531_381+532dup others(2): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr13 | 114240011 | ||||||
| chr13:114240011 | TA | T | 81 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(78): Show |
132 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.381+532delA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr13 | 114240011 | ||||||
| chr13:114240019 | A | AG | 3 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 |
3 | HG01109.hp1 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.381+529_381+530ins others(1): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240019 | |||||||
| chr13:114240169 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.381+679G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240169 | |||||||
| chr13:114240184 | C | G | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.381+694C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240184 | |||||||
| chr13:114240211 | C | CTT | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.381+730_381+731dup others(2): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr13 | 114240211 | ||||||
| chr13:114240235 | G | T | 1 | a0001c0002t0002g0013 | 5 | HG01891.hp1 HG02622.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+745G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240235 | |||||||
| chr13:114240272 | C | T | 1 | a0001c0002t0002g0046 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.381+782C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240272 | |||||||
| chr13:114240298 | C | A | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.381+808C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240298 | |||||||
| chr13:114240323 | C | T | 1 | a0001c0003t0004g0021 | 3 | HG00735.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.381+833C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240323 | |||||||
| chr13:114240400 | G | A | 1 | a0001c0004t0003g0069 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.381+910G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240400 | |||||||
| chr13:114240456 | A | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.381+966A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240456 | |||||||
| chr13:114240461 | G | T | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.381+971G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240461 | |||||||
| chr13:114240504 | C | G | 74 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(71): Show |
122 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.381+1014C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240504 | |||||||
| chr13:114240719 | T | A | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.381+1229T>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240719 | |||||||
| chr13:114240776 | A | G | 1 | a0001c0002t0002g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.381+1286A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240776 | |||||||
| chr13:114240807 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.382-1314C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240807 | |||||||
| chr13:114240971 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.382-1150G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240971 | |||||||
| chr13:114240975 | G | A | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.382-1146G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114240975 | |||||||
| chr13:114241023 | C | A | 73 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(70): Show |
121 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.382-1098C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241023 | |||||||
| chr13:114241031 | T | A | 6 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0179 others(3): Show |
9 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.382-1090T>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241031 | |||||||
| chr13:114241096 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.382-1025C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241096 | |||||||
| chr13:114241155 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.382-966G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241155 | |||||||
| chr13:114241160 | T | G | 1 | a0001c0002t0002g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.382-961T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241160 | |||||||
| chr13:114241260 | T | C | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.382-861T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241260 | |||||||
| chr13:114241286 | T | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(144): Show |
247 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.382-835T>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241286 | |||||||
| chr13:114241359 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.382-762C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241359 | |||||||
| chr13:114241376 | T | C | 89 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(86): Show |
150 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(147): Show |
intron_variant | MODIFIER | c.382-745T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241376 | |||||||
| chr13:114241457 | T | C | 73 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(70): Show |
121 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.382-664T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241457 | |||||||
| chr13:114241581 | T | C | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.382-540T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241581 | |||||||
| chr13:114241614 | A | G | 88 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(85): Show |
149 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.382-507A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | chr13 | 114241614 | |||||||
| chr13:114242058 | G | GA | 6 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0179 others(3): Show |
9 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.382-52dupA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr13 | 114242058 | ||||||
| chr13:114242353 | C | G | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.541+73C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 6/17 | chr13 | 114242353 | |||||||
| chr13:114242418 | A | C | 1 | a0001c0002t0008g0019 | 3 | HG02258.hp2 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.541+138A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 6/17 | chr13 | 114242418 | |||||||
| chr13:114242563 | A | G | 74 | a0001c0001t0001g0137 a0001c0002t0002g0004 a0001c0002t0002g0008 others(71): Show |
122 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.541+283A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 6/17 | chr13 | 114242563 | |||||||
| chr13:114242603 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.541+323T>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 6/17 | chr13 | 114242603 | |||||||
| chr13:114242632 | A | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.541+352A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 6/17 | chr13 | 114242632 | |||||||
| chr13:114242635 | C | T | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.541+355C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 6/17 | chr13 | 114242635 | |||||||
| chr13:114242713 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG00099.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.541+433C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 6/17 | chr13 | 114242713 | |||||||
| chr13:114242843 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.542-414C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 6/17 | chr13 | 114242843 | |||||||
| chr13:114242913 | T | C | 90 | a0001c0001t0001g0082 a0001c0002t0002g0004 a0001c0002t0002g0008 others(87): Show |
151 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(148): Show |
intron_variant | MODIFIER | c.542-344T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 6/17 | chr13 | 114242913 | |||||||
| chr13:114243207 | C | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.542-50C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 6/17 | chr13 | 114243207 | |||||||
| chr13:114243401 | A | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.633+53A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 7/17 | chr13 | 114243401 | |||||||
| chr13:114243514 | T | C | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.633+166T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 7/17 | chr13 | 114243514 | |||||||
| chr13:114243586 | T | C | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.633+238T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 7/17 | chr13 | 114243586 | |||||||
| chr13:114243683 | G | C | 3 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 |
3 | HG01109.hp1 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.634-173G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 7/17 | chr13 | 114243683 | |||||||
| chr13:114244040 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.767+51T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244040 | |||||||
| chr13:114244046 | G | C | 5 | a0001c0003t0004g0144 a0001c0003t0004g0145 a0001c0003t0004g0146 others(2): Show |
5 | HG02818.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.767+57G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244046 | |||||||
| chr13:114244058 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.767+69A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244058 | |||||||
| chr13:114244111 | A | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.767+122A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244111 | |||||||
| chr13:114244294 | AT | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.767+306delT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244294 | |||||||
| chr13:114244435 | G | A | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.767+446G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244435 | |||||||
| chr13:114244551 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.768-339G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244551 | |||||||
| chr13:114244566 | A | G | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.768-324A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244566 | |||||||
| chr13:114244629 | T | C | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.768-261T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244629 | |||||||
| chr13:114244779 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(76): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.768-111C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244779 | |||||||
| chr13:114244834 | C | T | 4 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 others(1): Show |
4 | HG01109.hp1 HG02809.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.768-56C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244834 | |||||||
| chr13:114244855 | G | T | 63 | a0001c0001t0001g0082 a0001c0001t0001g0134 a0001c0002t0002g0008 others(60): Show |
109 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.768-35G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244855 | |||||||
| chr13:114244863 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.768-27G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 8/17 | chr13 | 114244863 | |||||||
| chr13:114244980 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.847+11T>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114244980 | |||||||
| chr13:114245130 | A | G | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.847+161A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245130 | |||||||
| chr13:114245262 | T | TC | 12 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0002t0002g0025 others(9): Show |
20 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.847+302dupC | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr13 | 114245262 | ||||||
| chr13:114245270 | C | G | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.847+301C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245270 | |||||||
| chr13:114245271 | C | T | 7 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0178 others(4): Show |
10 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.847+302C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245271 | |||||||
| chr13:114245272 | T | C | 46 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0002t0002g0008 others(43): Show |
72 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.847+303T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245272 | |||||||
| chr13:114245273 | T | C | 1 | a0001c0002t0002g0045 | 2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.847+304T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245273 | |||||||
| chr13:114245386 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.847+417C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245386 | |||||||
| chr13:114245439 | G | C | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.847+470G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245439 | |||||||
| chr13:114245512 | C | T | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.848-488C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245512 | |||||||
| chr13:114245671 | G | T | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.848-329G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245671 | |||||||
| chr13:114245738 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0092 |
3 | HG01069.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.848-262A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245738 | |||||||
| chr13:114245772 | G | A | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.848-228G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245772 | |||||||
| chr13:114245777 | C | A | 1 | a0001c0005t0006g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.848-223C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245777 | |||||||
| chr13:114245777 | C | T | 6 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0179 others(3): Show |
9 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.848-223C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245777 | |||||||
| chr13:114245785 | G | A | 3 | a0001c0002t0007g0048 a0001c0002t0007g0213 a0001c0002t0007g0214 |
4 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.848-215G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245785 | |||||||
| chr13:114245828 | C | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0187 |
3 | HG00621.hp1 HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.848-172C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245828 | |||||||
| chr13:114245931 | G | A | 3 | a0001c0005t0006g0020 a0001c0005t0006g0078 a0001c0005t0006g0079 |
5 | HG01496.hp2 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.848-69G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245931 | |||||||
| chr13:114245941 | C | A | 1 | a0001c0002t0012g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.848-59C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245941 | |||||||
| chr13:114245964 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.848-36C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 9/17 | chr13 | 114245964 | |||||||
| chr13:114246075 | G | GT | 12 | a0001c0001t0001g0095 a0001c0001t0001g0131 a0001c0001t0001g0150 others(9): Show |
17 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.897+39dupT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr13 | 114246075 | ||||||
| chr13:114246075 | G | T | 1 | a0001c0002t0012g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.897+26G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 10/17 | chr13 | 114246075 | |||||||
| chr13:114246075 | GT | G | 6 | a0001c0001t0001g0101 a0001c0002t0002g0201 a0001c0002t0011g0076 others(3): Show |
11 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.897+39delT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr13 | 114246075 | ||||||
| chr13:114246321 | G | A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0005t0005g0005 others(1): Show |
9 | HG01069.hp1 HG01071.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.897+272G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 10/17 | chr13 | 114246321 | |||||||
| chr13:114246379 | G | A | 2 | a0001c0002t0002g0195 a0001c0002t0002g0196 |
2 | HG00733.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.897+330G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 10/17 | chr13 | 114246379 | |||||||
| chr13:114246469 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.897+420G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 10/17 | chr13 | 114246469 | |||||||
| chr13:114246495 | G | T | 1 | a0001c0001t0001g0173 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.898-436G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 10/17 | chr13 | 114246495 | |||||||
| chr13:114246716 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.898-215C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 10/17 | chr13 | 114246716 | |||||||
| chr13:114247115 | GT | G | 21 | a0001c0001t0001g0154 a0001c0002t0002g0017 a0001c0002t0002g0043 others(18): Show |
31 | HG00733.hp2 HG00738.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.971+122delT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114247115 | ||||||
| chr13:114247148 | C | CT | 6 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.971+147dupT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114247148 | ||||||
| chr13:114247217 | G | T | 76 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(73): Show |
126 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.971+213G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247217 | |||||||
| chr13:114247226 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0130 a0001c0001t0001g0140 |
4 | HG00099.hp1 HG00140.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.971+222A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247226 | |||||||
| chr13:114247287 | C | T | 6 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0179 others(3): Show |
9 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.971+283C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247287 | |||||||
| chr13:114247303 | C | T | 76 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(73): Show |
126 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.971+299C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247303 | |||||||
| chr13:114247333 | A | AT | 129 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(126): Show |
217 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.971+344dupT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114247333 | ||||||
| chr13:114247333 | A | ATT | 5 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0002t0008g0019 others(2): Show |
7 | HG01109.hp1 HG02258.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.971+343_971+344dup others(2): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114247333 | ||||||
| chr13:114247333 | A | T | 1 | a0001c0003t0001g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.971+329A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247333 | |||||||
| chr13:114247419 | C | T | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.971+415C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247419 | |||||||
| chr13:114247420 | G | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(36): Show |
73 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.971+416G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247420 | |||||||
| chr13:114247426 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG00558.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.971+422C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247426 | |||||||
| chr13:114247553 | T | C | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.971+549T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247553 | |||||||
| chr13:114247558 | A | G | 76 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(73): Show |
126 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.971+554A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247558 | |||||||
| chr13:114247580 | A | G | 6 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.971+576A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247580 | |||||||
| chr13:114247597 | G | A | 3 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 |
3 | HG01109.hp1 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.971+593G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247597 | |||||||
| chr13:114247645 | A | G | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.971+641A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247645 | |||||||
| chr13:114247745 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.971+741T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247745 | |||||||
| chr13:114247830 | C | T | 1 | a0001c0002t0012g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.971+826C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247830 | |||||||
| chr13:114247878 | A | AAATAAT | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+876_971+877ins others(6): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114247878 | ||||||
| chr13:114247881 | A | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+877A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247881 | |||||||
| chr13:114247948 | TTCTC | T | 76 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(73): Show |
126 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.971+948_971+951del others(4): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114247948 | ||||||
| chr13:114247958 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.971+954C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114247958 | |||||||
| chr13:114248198 | GAATT | G | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0002t0002g0197 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.971+1200_971+1203d others(6): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114248198 | ||||||
| chr13:114248277 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+1273G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248277 | |||||||
| chr13:114248279 | A | C | 1 | a0001c0001t0001g0128 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.971+1275A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248279 | |||||||
| chr13:114248339 | T | C | 1 | a0001c0004t0003g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.971+1335T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248339 | |||||||
| chr13:114248406 | C | T | 3 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 |
3 | HG01109.hp1 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.971+1402C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248406 | |||||||
| chr13:114248435 | C | T | 1 | a0001c0002t0002g0045 | 2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.971+1431C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248435 | |||||||
| chr13:114248478 | C | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+1474C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248478 | |||||||
| chr13:114248538 | G | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+1534G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248538 | |||||||
| chr13:114248540 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(144): Show |
247 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.971+1536A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248540 | |||||||
| chr13:114248557 | T | C | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+1553T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248557 | |||||||
| chr13:114248561 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.971+1557A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248561 | |||||||
| chr13:114248573 | T | C | 12 | a0001c0002t0009g0024 a0001c0004t0003g0010 a0001c0004t0003g0030 others(9): Show |
23 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.971+1569T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248573 | |||||||
| chr13:114248646 | A | G | 5 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0069 others(2): Show |
10 | HG00642.hp1 HG01361.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.971+1642A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248646 | |||||||
| chr13:114248701 | G | A | 7 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0178 others(4): Show |
10 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.971+1697G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248701 | |||||||
| chr13:114248758 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.971+1754A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248758 | |||||||
| chr13:114248975 | G | A | 1 | a0001c0009t0001g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.972-1574G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114248975 | |||||||
| chr13:114249005 | C | T | 2 | a0001c0002t0002g0049 a0001c0002t0002g0192 |
3 | HG02145.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.972-1544C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249005 | |||||||
| chr13:114249006 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-1543G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249006 | |||||||
| chr13:114249019 | C | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-1530C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249019 | |||||||
| chr13:114249024 | G | A | 107 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(104): Show |
173 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.972-1525G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249024 | |||||||
| chr13:114249125 | T | C | 30 | a0001c0002t0002g0004 a0001c0002t0002g0018 a0001c0002t0002g0025 others(27): Show |
51 | HG00735.hp1 HG00738.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.972-1424T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249125 | |||||||
| chr13:114249196 | G | A | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.972-1353G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249196 | |||||||
| chr13:114249221 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-1328G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249221 | |||||||
| chr13:114249264 | G | T | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.972-1285G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249264 | |||||||
| chr13:114249332 | C | CT | 4 | a0001c0003t0001g0182 a0001c0003t0001g0183 a0001c0005t0005g0005 others(1): Show |
9 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.972-1205dupT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114249332 | ||||||
| chr13:114249332 | CT | C | 75 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(72): Show |
125 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.972-1205delT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114249332 | ||||||
| chr13:114249439 | T | C | 12 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0023 others(9): Show |
26 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.972-1110T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249439 | |||||||
| chr13:114249531 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.972-1018G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249531 | |||||||
| chr13:114249587 | G | A | 1 | a0001c0002t0007g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.972-962G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249587 | |||||||
| chr13:114249642 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-907G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249642 | |||||||
| chr13:114249688 | C | T | 76 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(73): Show |
126 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.972-861C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249688 | |||||||
| chr13:114249902 | A | G | 5 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0180 others(2): Show |
8 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-647A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249902 | |||||||
| chr13:114249909 | A | T | 1 | a0001c0001t0001g0125 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.972-640A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249909 | |||||||
| chr13:114249926 | A | T | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.972-623A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114249926 | |||||||
| chr13:114249955 | TGTG | T | 12 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0023 others(9): Show |
26 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.972-590_972-588del others(3): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114249955 | ||||||
| chr13:114250027 | C | G | 1 | a0001c0001t0001g0034 | 2 | HG00099.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.972-522C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114250027 | |||||||
| chr13:114250102 | T | C | 101 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(98): Show |
165 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.972-447T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114250102 | |||||||
| chr13:114250147 | C | T | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.972-402C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114250147 | |||||||
| chr13:114250190 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.972-359A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114250190 | |||||||
| chr13:114250305 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(13): Show |
33 | HG00544.hp1 HG00609.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.972-244C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114250305 | |||||||
| chr13:114250349 | G | A | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.972-200G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114250349 | |||||||
| chr13:114250404 | A | T | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.972-145A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114250404 | |||||||
| chr13:114250423 | C | T | 1 | a0001c0002t0002g0045 | 2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.972-126C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114250423 | |||||||
| chr13:114250468 | A | G | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-81A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | chr13 | 114250468 | |||||||
| chr13:114250491 | C | CA | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(66): Show |
115 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.972-42dupA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114250491 | ||||||
| chr13:114250491 | C | CAA | 4 | a0001c0001t0001g0155 a0001c0003t0004g0145 a0001c0005t0005g0005 others(1): Show |
9 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.972-43_972-42dupAA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr13 | 114250491 | ||||||
| chr13:114250740 | A | G | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1097+66A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114250740 | |||||||
| chr13:114250976 | C | T | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1097+302C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114250976 | |||||||
| chr13:114251018 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1097+344G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251018 | |||||||
| chr13:114251036 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1097+362G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251036 | |||||||
| chr13:114251132 | C | T | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1097+458C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251132 | |||||||
| chr13:114251140 | C | A | 1 | a0001c0002t0002g0195 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1097+466C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251140 | |||||||
| chr13:114251163 | C | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0167 a0001c0001t0001g0187 |
4 | HG00621.hp1 HG02080.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1097+489C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251163 | |||||||
| chr13:114251628 | A | G | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1097+954A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251628 | |||||||
| chr13:114251688 | G | T | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1097+1014G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251688 | |||||||
| chr13:114251747 | G | A | 6 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0179 others(3): Show |
9 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1097+1073G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251747 | |||||||
| chr13:114251769 | T | C | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1097+1095T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251769 | |||||||
| chr13:114251807 | C | T | 3 | a0001c0002t0009g0024 a0001c0005t0005g0005 a0001c0005t0006g0077 |
9 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.1097+1133C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251807 | |||||||
| chr13:114251837 | C | G | 5 | a0001c0003t0004g0144 a0001c0003t0004g0145 a0001c0003t0004g0146 others(2): Show |
5 | HG02818.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1097+1163C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251837 | |||||||
| chr13:114251840 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1097+1166G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251840 | |||||||
| chr13:114251913 | T | TTACACTA others(20): Show |
1 | a0001c0009t0001g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1097+1301_1097+132 others(31): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114251913 | ||||||
| chr13:114251913 | TTACACTA others(20): Show |
T | 2 | a0001c0002t0002g0056 a0001c0007t0002g0223 |
2 | HG01433.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1097+1301_1097+132 others(31): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114251913 | ||||||
| chr13:114251924 | C | G | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1097+1250C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251924 | |||||||
| chr13:114251937 | G | C | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1097+1263G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251937 | |||||||
| chr13:114251967 | C | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097+1293C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251967 | |||||||
| chr13:114251967 | CTACACTA others(101): Show |
C | 1 | a0001c0001t0001g0124 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1097+1328_1097+143 others(4): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114251967 | ||||||
| chr13:114251970 | C | T | 3 | a0001c0002t0002g0198 a0001c0005t0005g0005 a0001c0005t0006g0077 |
8 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1097+1296C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251970 | |||||||
| chr13:114251975 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097+1301G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251975 | |||||||
| chr13:114251975 | G | GCCCTGTT others(20): Show |
1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1097+1320_1097+132 others(31): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114251975 | ||||||
| chr13:114251994 | C | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097+1320C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251994 | |||||||
| chr13:114251995 | T | C | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1097+1321T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114251995 | |||||||
| chr13:114252002 | A | G | 3 | a0001c0001t0001g0123 a0001c0005t0005g0005 a0001c0005t0006g0077 |
8 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1097+1328A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252002 | |||||||
| chr13:114252021 | T | C | 3 | a0001c0001t0001g0123 a0001c0005t0005g0005 a0001c0005t0006g0077 |
8 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1097+1347T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252021 | |||||||
| chr13:114252029 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1097+1355G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252029 | |||||||
| chr13:114252048 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1097+1374C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252048 | |||||||
| chr13:114252056 | A | ACCCTGTT others(74): Show |
1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1097+1386_1097+138 others(85): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114252056 | ||||||
| chr13:114252056 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0123 |
2 | HG03927.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1097+1382A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252056 | |||||||
| chr13:114252061 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(51): Show |
92 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1097+1387A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252061 | |||||||
| chr13:114252075 | T | C | 3 | a0001c0001t0001g0123 a0001c0002t0002g0056 a0001c0002t0011g0076 |
3 | HG01433.hp2 NA19058.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1097+1401T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252075 | |||||||
| chr13:114252075 | T | TTACACTA others(182): Show |
1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1097+1562_1097+156 others(193): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114252075 | ||||||
| chr13:114252075 | T | TTACACTA others(290): Show |
2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097+1481_1097+148 others(301): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114252075 | ||||||
| chr13:114252075 | TTACACTA others(20): Show |
T | 6 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0003t0004g0144 others(3): Show |
6 | HG02818.hp1 HG02895.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1097+1536_1097+156 others(31): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114252075 | ||||||
| chr13:114252083 | G | A | 2 | a0001c0001t0001g0123 a0001c0002t0002g0056 |
2 | HG01433.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1097+1409G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252083 | |||||||
| chr13:114252088 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1097+1414G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252088 | |||||||
| chr13:114252102 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1097+1428C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252102 | |||||||
| chr13:114252109 | A | AGCCCTGT others(290): Show |
3 | a0001c0004t0003g0052 a0001c0004t0003g0070 a0001c0004t0003g0071 |
3 | HG01993.hp1 HG02004.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1097+1562_1097+156 others(301): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114252109 | ||||||
| chr13:114252136 | A | AGCCCTGT others(290): Show |
5 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0068 others(2): Show |
10 | HG00642.hp1 HG01361.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.1097+1562_1097+156 others(301): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114252136 | ||||||
| chr13:114252141 | T | C | 3 | a0001c0005t0006g0020 a0001c0005t0006g0078 a0001c0005t0006g0079 |
5 | HG01496.hp2 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097+1467T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252141 | |||||||
| chr13:114252187 | A | G | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1097+1513A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252187 | |||||||
| chr13:114252190 | A | AGCCCTGT others(290): Show |
1 | a0001c0004t0003g0073 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1097+1562_1097+156 others(301): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114252190 | ||||||
| chr13:114252237 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1097+1563T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252237 | |||||||
| chr13:114252276 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1097+1602T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252276 | |||||||
| chr13:114252414 | G | T | 1 | a0001c0002t0002g0210 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1097+1740G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252414 | |||||||
| chr13:114252430 | A | G | 1 | a0001c0002t0002g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1097+1756A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252430 | |||||||
| chr13:114252581 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1097+1907C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252581 | |||||||
| chr13:114252643 | C | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097+1969C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252643 | |||||||
| chr13:114252644 | C | CA | 7 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0178 others(4): Show |
10 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1097+1980dupA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114252644 | ||||||
| chr13:114252651 | AAAAT | A | 75 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(72): Show |
125 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.1097+1978_1097+198 others(8): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252651 | |||||||
| chr13:114252660 | A | G | 1 | a0001c0002t0002g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1097+1986A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252660 | |||||||
| chr13:114252675 | T | G | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1097+2001T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252675 | |||||||
| chr13:114252822 | A | C | 23 | a0001c0002t0002g0004 a0001c0002t0002g0025 a0001c0002t0002g0026 others(20): Show |
38 | HG00735.hp1 HG00738.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1097+2148A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252822 | |||||||
| chr13:114252933 | A | G | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097+2259A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252933 | |||||||
| chr13:114252983 | T | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(174): Show |
300 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.1097+2309T>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252983 | |||||||
| chr13:114252995 | G | C | 1 | a0001c0002t0002g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1097+2321G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114252995 | |||||||
| chr13:114253060 | A | G | 1 | a0001c0002t0002g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1097+2386A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253060 | |||||||
| chr13:114253077 | G | T | 3 | a0001c0005t0006g0020 a0001c0005t0006g0078 a0001c0005t0006g0079 |
5 | HG01496.hp2 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097+2403G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253077 | |||||||
| chr13:114253084 | G | C | 1 | a0001c0003t0001g0180 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1097+2410G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253084 | |||||||
| chr13:114253094 | A | G | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097+2420A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253094 | |||||||
| chr13:114253231 | G | A | 4 | a0001c0002t0002g0018 a0001c0002t0002g0031 a0001c0002t0002g0032 others(1): Show |
8 | HG03491.hp2 HG03704.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.1097+2557G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253231 | |||||||
| chr13:114253372 | C | T | 1 | a0001c0002t0002g0194 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1097+2698C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253372 | |||||||
| chr13:114253373 | G | A | 9 | a0001c0002t0002g0017 a0001c0002t0002g0045 a0001c0002t0002g0195 others(6): Show |
13 | HG00733.hp2 HG01243.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1097+2699G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253373 | |||||||
| chr13:114253411 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1097+2737G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253411 | |||||||
| chr13:114253425 | A | C | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1097+2751A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253425 | |||||||
| chr13:114253436 | C | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097+2762C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253436 | |||||||
| chr13:114253567 | G | T | 7 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0178 others(4): Show |
10 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1097+2893G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253567 | |||||||
| chr13:114253614 | C | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(36): Show |
73 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1097+2940C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253614 | |||||||
| chr13:114253615 | A | G | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097+2941A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253615 | |||||||
| chr13:114253616 | G | A | 1 | a0001c0002t0002g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1097+2942G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253616 | |||||||
| chr13:114253643 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1097+2969C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253643 | |||||||
| chr13:114253644 | G | A | 1 | a0001c0006t0010g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1097+2970G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253644 | |||||||
| chr13:114253688 | C | CA | 77 | a0001c0001t0001g0108 a0001c0001t0001g0169 a0001c0002t0002g0004 others(74): Show |
127 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1097+3028dupA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114253688 | ||||||
| chr13:114253688 | CA | C | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097+3028delA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114253688 | ||||||
| chr13:114253720 | CTTT | C | 73 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(70): Show |
122 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.1097+3050_1097+305 others(7): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114253720 | ||||||
| chr13:114253726 | T | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0154 a0001c0001t0001g0157 others(2): Show |
8 | HG02040.hp2 NA18959.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.1097+3052T>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253726 | |||||||
| chr13:114253793 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1097+3119T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253793 | |||||||
| chr13:114253803 | T | C | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1097+3129T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253803 | |||||||
| chr13:114253883 | A | G | 1 | a0001c0001t0001g0041 | 2 | HG00558.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1098-3195A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253883 | |||||||
| chr13:114253923 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1098-3155G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253923 | |||||||
| chr13:114253942 | C | T | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1098-3136C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253942 | |||||||
| chr13:114253991 | A | G | 73 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(70): Show |
122 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.1098-3087A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114253991 | |||||||
| chr13:114254050 | CTAAT | C | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-3025_1098-302 others(8): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114254050 | ||||||
| chr13:114254070 | T | C | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098-3008T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254070 | |||||||
| chr13:114254177 | G | T | 1 | a0001c0009t0001g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1098-2901G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254177 | |||||||
| chr13:114254266 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-2812G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254266 | |||||||
| chr13:114254288 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0124 a0001c0001t0001g0131 others(1): Show |
7 | NA18940.hp2 NA18947.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-2790C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254288 | |||||||
| chr13:114254329 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1098-2749T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254329 | |||||||
| chr13:114254336 | T | A | 1 | a0001c0001t0001g0109 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1098-2742T>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254336 | |||||||
| chr13:114254371 | A | G | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-2707A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254371 | |||||||
| chr13:114254435 | T | C | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-2643T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254435 | |||||||
| chr13:114254466 | T | G | 76 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(73): Show |
126 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.1098-2612T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254466 | |||||||
| chr13:114254543 | T | C | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098-2535T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254543 | |||||||
| chr13:114254599 | T | C | 1 | a0001c0003t0001g0178 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1098-2479T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254599 | |||||||
| chr13:114254834 | T | G | 79 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(76): Show |
135 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(132): Show |
intron_variant | MODIFIER | c.1098-2244T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254834 | |||||||
| chr13:114254844 | G | A | 80 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(77): Show |
136 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.1098-2234G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254844 | |||||||
| chr13:114254941 | C | T | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1098-2137C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114254941 | |||||||
| chr13:114255036 | C | A | 11 | a0001c0002t0002g0017 a0001c0002t0002g0045 a0001c0002t0002g0195 others(8): Show |
15 | HG00733.hp2 HG00738.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1098-2042C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255036 | |||||||
| chr13:114255098 | G | A | 1 | a0001c0005t0006g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1098-1980G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255098 | |||||||
| chr13:114255127 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-1951G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255127 | |||||||
| chr13:114255134 | C | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-1944C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255134 | |||||||
| chr13:114255160 | T | C | 1 | a0001c0003t0001g0022 | 3 | HG00741.hp2 HG01123.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1098-1918T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255160 | |||||||
| chr13:114255209 | T | G | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-1869T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255209 | |||||||
| chr13:114255240 | G | A | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1098-1838G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255240 | |||||||
| chr13:114255325 | T | C | 1 | a0001c0002t0002g0018 | 3 | HG03831.hp1 HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1098-1753T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255325 | |||||||
| chr13:114255482 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1098-1596C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255482 | |||||||
| chr13:114255543 | A | C | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1098-1535A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255543 | |||||||
| chr13:114255591 | T | TAA | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-1476_1098-147 others(6): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr13 | 114255591 | ||||||
| chr13:114255644 | G | A | 84 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(81): Show |
139 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.1098-1434G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255644 | |||||||
| chr13:114255743 | A | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-1335A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255743 | |||||||
| chr13:114255806 | C | A | 1 | a0001c0005t0006g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1098-1272C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255806 | |||||||
| chr13:114255923 | G | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-1155G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255923 | |||||||
| chr13:114255935 | G | A | 1 | a0001c0002t0002g0056 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1098-1143G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114255935 | |||||||
| chr13:114256188 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG00140.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1098-890G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256188 | |||||||
| chr13:114256247 | G | C | 12 | a0001c0002t0009g0024 a0001c0004t0003g0010 a0001c0004t0003g0030 others(9): Show |
23 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1098-831G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256247 | |||||||
| chr13:114256380 | T | C | 4 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 others(1): Show |
4 | HG01109.hp1 HG02809.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098-698T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256380 | |||||||
| chr13:114256539 | C | G | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098-539C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256539 | |||||||
| chr13:114256602 | C | G | 1 | a0001c0003t0004g0021 | 3 | HG00735.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1098-476C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256602 | |||||||
| chr13:114256679 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1098-399C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256679 | |||||||
| chr13:114256696 | G | C | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-382G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256696 | |||||||
| chr13:114256706 | A | G | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-372A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256706 | |||||||
| chr13:114256719 | A | G | 1 | a0001c0002t0002g0210 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1098-359A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256719 | |||||||
| chr13:114256799 | A | G | 1 | a0001c0002t0002g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1098-279A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256799 | |||||||
| chr13:114256867 | A | C | 3 | a0001c0003t0004g0145 a0001c0003t0004g0147 a0001c0003t0004g0148 |
3 | HG02818.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1098-211A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256867 | |||||||
| chr13:114256896 | C | T | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1098-182C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 12/17 | chr13 | 114256896 | |||||||
| chr13:114257573 | A | C | 1 | a0001c0002t0002g0074 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1250+343A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114257573 | |||||||
| chr13:114257811 | G | T | 76 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(73): Show |
126 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.1250+581G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114257811 | |||||||
| chr13:114257817 | C | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+587C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114257817 | |||||||
| chr13:114257889 | C | T | 2 | a0001c0003t0001g0189 a0001c0006t0010g0211 |
2 | HG00621.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1250+659C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114257889 | |||||||
| chr13:114257898 | T | C | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1250+668T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114257898 | |||||||
| chr13:114257910 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1250+680C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114257910 | |||||||
| chr13:114258007 | G | A | 7 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0178 others(4): Show |
10 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1250+777G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114258007 | |||||||
| chr13:114258099 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1250+869A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114258099 | |||||||
| chr13:114258182 | A | C | 6 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1250+952A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114258182 | |||||||
| chr13:114258217 | A | G | 3 | a0001c0001t0001g0040 a0001c0002t0002g0049 a0001c0002t0002g0192 |
5 | HG02145.hp1 HG02148.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250+987A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114258217 | |||||||
| chr13:114258445 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1251-890A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114258445 | |||||||
| chr13:114258740 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-595G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114258740 | |||||||
| chr13:114258773 | C | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-562C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114258773 | |||||||
| chr13:114258786 | CACAGTGA others(5): Show |
C | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1251-548_1251-537d others(14): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114258786 | |||||||
| chr13:114258864 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-471G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114258864 | |||||||
| chr13:114259054 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-281G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114259054 | |||||||
| chr13:114259078 | A | G | 12 | a0001c0002t0009g0024 a0001c0004t0003g0010 a0001c0004t0003g0030 others(9): Show |
23 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1251-257A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114259078 | |||||||
| chr13:114259094 | T | TA | 18 | a0001c0001t0001g0085 a0001c0001t0001g0111 a0001c0001t0001g0141 others(15): Show |
25 | HG00642.hp1 HG00733.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1251-221dupA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr13 | 114259094 | ||||||
| chr13:114259094 | TA | T | 15 | a0001c0001t0001g0090 a0001c0001t0001g0153 a0001c0001t0001g0165 others(12): Show |
18 | HG01070.hp2 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.1251-221delA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr13 | 114259094 | ||||||
| chr13:114259094 | TAA | T | 6 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1251-222_1251-221d others(4): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr13 | 114259094 | ||||||
| chr13:114259094 | TAAAAA | T | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-225_1251-221d others(7): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr13 | 114259094 | ||||||
| chr13:114259191 | T | C | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1251-144T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 13/17 | chr13 | 114259191 | |||||||
| chr13:114259595 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1314+197A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114259595 | |||||||
| chr13:114259645 | G | T | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1314+247G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114259645 | |||||||
| chr13:114259698 | G | A | 1 | a0001c0006t0010g0211 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1314+300G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114259698 | |||||||
| chr13:114259923 | G | A | 76 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(73): Show |
126 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.1314+525G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114259923 | |||||||
| chr13:114260159 | G | A | 6 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0179 others(3): Show |
9 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1314+761G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260159 | |||||||
| chr13:114260297 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1314+899T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260297 | |||||||
| chr13:114260326 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1314+928G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260326 | |||||||
| chr13:114260423 | C | A | 3 | a0001c0002t0007g0048 a0001c0002t0007g0213 a0001c0002t0007g0214 |
4 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1314+1025C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260423 | |||||||
| chr13:114260430 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1314+1032C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260430 | |||||||
| chr13:114260473 | G | A | 2 | a0001c0005t0005g0005 a0001c0005t0006g0077 |
7 | HG01069.hp1 HG01071.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1314+1075G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260473 | |||||||
| chr13:114260578 | A | C | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1314+1180A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260578 | |||||||
| chr13:114260615 | A | C | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1314+1217A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260615 | |||||||
| chr13:114260712 | G | T | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1315-1175G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260712 | |||||||
| chr13:114260714 | A | C | 3 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 |
3 | HG01109.hp1 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1315-1173A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260714 | |||||||
| chr13:114260830 | A | G | 23 | a0001c0002t0002g0004 a0001c0002t0002g0025 a0001c0002t0002g0026 others(20): Show |
38 | HG00735.hp1 HG00738.hp1 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1315-1057A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260830 | |||||||
| chr13:114260982 | G | A | 1 | a0001c0002t0002g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1315-905G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114260982 | |||||||
| chr13:114261029 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1315-858A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114261029 | |||||||
| chr13:114261167 | T | G | 2 | a0001c0002t0002g0197 a0001c0002t0002g0199 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1315-720T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114261167 | |||||||
| chr13:114261435 | G | A | 1 | a0001c0005t0006g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1315-452G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114261435 | |||||||
| chr13:114261659 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG00099.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.1315-228G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114261659 | |||||||
| chr13:114261733 | A | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG00280.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1315-154A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114261733 | |||||||
| chr13:114261752 | C | A | 7 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0178 others(4): Show |
10 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1315-135C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114261752 | |||||||
| chr13:114261753 | C | T | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1315-134C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114261753 | |||||||
| chr13:114261775 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0172 |
2 | NA18979.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1315-112G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114261775 | |||||||
| chr13:114261860 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1315-27C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 14/17 | chr13 | 114261860 | |||||||
| chr13:114261987 | T | A | 89 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(86): Show |
150 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(147): Show |
intron_variant | MODIFIER | c.1376+39T>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114261987 | |||||||
| chr13:114262013 | C | T | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1376+65C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114262013 | |||||||
| chr13:114262041 | A | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(49): Show |
89 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1376+93A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114262041 | |||||||
| chr13:114262072 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1376+124A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114262072 | |||||||
| chr13:114262266 | A | C | 1 | a0001c0002t0002g0018 | 3 | HG03831.hp1 HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1376+318A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114262266 | |||||||
| chr13:114262284 | G | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0014 others(25): Show |
51 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1376+336G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114262284 | |||||||
| chr13:114262286 | G | T | 2 | a0001c0003t0002g0184 a0001c0003t0002g0185 |
2 | HG02818.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1376+338G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114262286 | |||||||
| chr13:114262334 | A | G | 2 | a0001c0002t0002g0049 a0001c0002t0002g0192 |
3 | HG02145.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1376+386A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114262334 | |||||||
| chr13:114262389 | T | C | 1 | a0001c0002t0002g0058 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1376+441T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114262389 | |||||||
| chr13:114262429 | T | TC | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1377-449dupC | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr13 | 114262429 | ||||||
| chr13:114262456 | TC | T | 1 | a0001c0002t0008g0019 | 3 | HG02258.hp2 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1377-421delC | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr13 | 114262456 | ||||||
| chr13:114262683 | G | A | 1 | a0001c0002t0012g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1377-196G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114262683 | |||||||
| chr13:114262736 | G | A | 1 | a0001c0001t0001g0036 | 2 | NA18957.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1377-143G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114262736 | |||||||
| chr13:114262748 | A | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1377-131A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 15/17 | chr13 | 114262748 | |||||||
| chr13:114263076 | A | G | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1512+62A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114263076 | |||||||
| chr13:114263298 | G | C | 8 | a0001c0002t0002g0008 a0001c0002t0002g0023 a0001c0002t0002g0047 others(5): Show |
16 | HG00639.hp1 HG01243.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1512+284G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114263298 | |||||||
| chr13:114263466 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1512+452A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114263466 | |||||||
| chr13:114263642 | A | G | 3 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 |
3 | HG01109.hp1 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1512+628A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114263642 | |||||||
| chr13:114263687 | G | A | 88 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(85): Show |
149 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.1512+673G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114263687 | |||||||
| chr13:114263767 | T | G | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1512+753T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114263767 | |||||||
| chr13:114263940 | C | A | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1512+926C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114263940 | |||||||
| chr13:114264056 | A | G | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1512+1042A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264056 | |||||||
| chr13:114264062 | G | A | 1 | a0001c0001t0001g0036 | 2 | NA18957.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1512+1048G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264062 | |||||||
| chr13:114264088 | A | T | 73 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(70): Show |
121 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.1513-1062A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264088 | |||||||
| chr13:114264109 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1513-1041T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264109 | |||||||
| chr13:114264219 | T | C | 1 | a0001c0005t0006g0078 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1513-931T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264219 | |||||||
| chr13:114264302 | C | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1513-848C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264302 | |||||||
| chr13:114264303 | A | G | 80 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(77): Show |
136 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.1513-847A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264303 | |||||||
| chr13:114264323 | A | G | 89 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(86): Show |
150 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(147): Show |
intron_variant | MODIFIER | c.1513-827A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264323 | |||||||
| chr13:114264328 | A | G | 1 | a0001c0009t0001g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1513-822A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264328 | |||||||
| chr13:114264381 | A | C | 1 | a0001c0002t0002g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1513-769A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264381 | |||||||
| chr13:114264431 | A | G | 1 | a0001c0008t0002g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1513-719A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264431 | |||||||
| chr13:114264445 | C | T | 1 | a0001c0003t0001g0181 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1513-705C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264445 | |||||||
| chr13:114264511 | G | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0156 a0001c0001t0001g0165 |
7 | NA18945.hp2 NA18953.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1513-639G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264511 | |||||||
| chr13:114264525 | AT | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(35): Show |
72 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1513-623delT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr13 | 114264525 | ||||||
| chr13:114264526 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1513-624T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264526 | |||||||
| chr13:114264545 | C | T | 6 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1513-605C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264545 | |||||||
| chr13:114264553 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1513-597T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264553 | |||||||
| chr13:114264902 | C | G | 1 | a0001c0004t0003g0072 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1513-248C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264902 | |||||||
| chr13:114264912 | T | C | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1513-238T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264912 | |||||||
| chr13:114264929 | T | C | 1 | a0001c0002t0002g0056 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1513-221T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114264929 | |||||||
| chr13:114265007 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1513-143A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114265007 | |||||||
| chr13:114265015 | T | C | 6 | a0001c0002t0009g0024 a0001c0005t0005g0005 a0001c0005t0006g0020 others(3): Show |
14 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1513-135T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114265015 | |||||||
| chr13:114265036 | A | G | 2 | a0001c0001t0001g0126 a0001c0002t0011g0076 |
2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1513-114A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 16/17 | chr13 | 114265036 | |||||||
| chr13:114265277 | A | C | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1603+37A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114265277 | |||||||
| chr13:114265818 | A | AT | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+592dupT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114265818 | ||||||
| chr13:114265818 | AT | A | 74 | a0001c0002t0002g0004 a0001c0002t0002g0008 a0001c0002t0002g0009 others(71): Show |
122 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.1603+592delT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114265818 | ||||||
| chr13:114265877 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1603+637G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114265877 | |||||||
| chr13:114265926 | C | T | 6 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+686C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114265926 | |||||||
| chr13:114265976 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+736T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114265976 | |||||||
| chr13:114266268 | C | T | 1 | a0001c0009t0001g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1603+1028C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114266268 | |||||||
| chr13:114266382 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+1142T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114266382 | |||||||
| chr13:114266466 | A | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(39): Show |
76 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1603+1226A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114266466 | |||||||
| chr13:114266698 | CT | C | 9 | a0001c0002t0002g0059 a0001c0002t0002g0060 a0001c0002t0009g0024 others(6): Show |
17 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1603+1471delT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114266698 | ||||||
| chr13:114266717 | G | A | 2 | a0001c0002t0002g0046 a0001c0002t0002g0212 |
3 | HG02486.hp2 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1603+1477G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114266717 | |||||||
| chr13:114266782 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0139 |
3 | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1603+1542C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114266782 | |||||||
| chr13:114266852 | C | T | 8 | a0001c0002t0002g0067 a0001c0003t0001g0022 a0001c0003t0001g0042 others(5): Show |
11 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1603+1612C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114266852 | |||||||
| chr13:114266954 | C | T | 1 | a0001c0002t0002g0204 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1603+1714C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114266954 | |||||||
| chr13:114267017 | G | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0166 |
8 | HG01123.hp2 HG01975.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1603+1777G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267017 | |||||||
| chr13:114267127 | A | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+1887A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267127 | |||||||
| chr13:114267253 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(144): Show |
247 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.1603+2013T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267253 | |||||||
| chr13:114267333 | A | G | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1603+2093A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267333 | |||||||
| chr13:114267342 | C | CA | 73 | a0001c0001t0001g0080 a0001c0002t0002g0004 a0001c0002t0002g0008 others(70): Show |
120 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(117): Show |
intron_variant | MODIFIER | c.1603+2111dupA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114267342 | ||||||
| chr13:114267351 | A | AG | 2 | a0001c0002t0002g0047 a0001c0002t0002g0209 |
3 | HG01243.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1603+2111_1603+211 others(5): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267351 | |||||||
| chr13:114267373 | C | T | 6 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+2133C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267373 | |||||||
| chr13:114267425 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1603+2185C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267425 | |||||||
| chr13:114267482 | C | CAG | 148 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(145): Show |
248 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.1603+2243_1603+224 others(6): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114267482 | ||||||
| chr13:114267498 | A | C | 4 | a0001c0002t0002g0018 a0001c0002t0002g0031 a0001c0002t0002g0032 others(1): Show |
8 | HG03491.hp2 HG03704.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+2258A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267498 | |||||||
| chr13:114267528 | T | G | 3 | a0001c0005t0006g0020 a0001c0005t0006g0078 a0001c0005t0006g0079 |
5 | HG01496.hp2 HG02109.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1603+2288T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267528 | |||||||
| chr13:114267536 | C | A | 3 | a0001c0002t0002g0025 a0001c0002t0002g0026 a0001c0002t0002g0054 |
5 | HG00735.hp1 HG00738.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603+2296C>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267536 | |||||||
| chr13:114267541 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1603+2301A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267541 | |||||||
| chr13:114267563 | G | C | 6 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1603+2323G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267563 | |||||||
| chr13:114267711 | G | A | 1 | a0001c0008t0002g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1603+2471G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267711 | |||||||
| chr13:114267717 | A | T | 1 | a0001c0003t0001g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1603+2477A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267717 | |||||||
| chr13:114267767 | G | GAGAGGAA others(24): Show |
5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+2529_1603+253 others(35): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114267767 | ||||||
| chr13:114267777 | C | CCAGCCTG | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+2538_1603+253 others(11): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114267777 | ||||||
| chr13:114267788 | TG | T | 3 | a0001c0002t0002g0027 a0001c0002t0002g0059 a0001c0002t0002g0061 |
4 | NA18968.hp2 NA18982.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603+2550delG | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114267788 | ||||||
| chr13:114267793 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1603+2553G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267793 | |||||||
| chr13:114267817 | A | G | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1603+2577A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267817 | |||||||
| chr13:114267888 | T | G | 43 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(40): Show |
77 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1603+2648T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267888 | |||||||
| chr13:114267942 | A | G | 1 | a0001c0002t0002g0063 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1603+2702A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267942 | |||||||
| chr13:114267971 | G | A | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1603+2731G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114267971 | |||||||
| chr13:114268117 | C | T | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1603+2877C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268117 | |||||||
| chr13:114268121 | T | C | 1 | a0001c0002t0002g0065 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1603+2881T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268121 | |||||||
| chr13:114268134 | AG | A | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+2902delG | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114268134 | ||||||
| chr13:114268143 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1603+2903A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268143 | |||||||
| chr13:114268159 | G | A | 1 | a0001c0002t0002g0023 | 3 | HG02572.hp1 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1603+2919G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268159 | |||||||
| chr13:114268202 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1603+2962A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268202 | |||||||
| chr13:114268237 | G | T | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1603+2997G>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268237 | |||||||
| chr13:114268325 | T | C | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1603+3085T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268325 | |||||||
| chr13:114268388 | A | T | 1 | a0001c0003t0001g0178 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1603+3148A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268388 | |||||||
| chr13:114268403 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1603+3163T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268403 | |||||||
| chr13:114268411 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+3171T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268411 | |||||||
| chr13:114268503 | A | G | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1603+3263A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268503 | |||||||
| chr13:114268529 | A | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+3289A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268529 | |||||||
| chr13:114268617 | C | G | 1 | a0001c0001t0001g0162 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1603+3377C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268617 | |||||||
| chr13:114268618 | G | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603+3378G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268618 | |||||||
| chr13:114268861 | A | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-3323A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114268861 | |||||||
| chr13:114269020 | A | C | 3 | a0001c0003t0001g0181 a0001c0003t0001g0182 a0001c0003t0001g0183 |
3 | HG01109.hp1 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1604-3164A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269020 | |||||||
| chr13:114269056 | C | CAAT | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-3128_1604-312 others(7): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269056 | |||||||
| chr13:114269255 | C | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-2929C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269255 | |||||||
| chr13:114269381 | G | GGGCTGTA others(12): Show |
5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-2796_1604-279 others(23): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114269381 | ||||||
| chr13:114269489 | G | A | 6 | a0001c0003t0001g0022 a0001c0003t0001g0042 a0001c0003t0001g0179 others(3): Show |
9 | HG00408.hp2 HG00621.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1604-2695G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269489 | |||||||
| chr13:114269595 | G | A | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-2589G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269595 | |||||||
| chr13:114269708 | T | TTTATTA | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-2473_1604-246 others(10): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114269708 | ||||||
| chr13:114269714 | A | AT | 3 | a0001c0002t0002g0027 a0001c0002t0002g0059 a0001c0002t0002g0061 |
4 | NA18968.hp2 NA18982.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1604-2464dupT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114269714 | ||||||
| chr13:114269744 | A | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-2440A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269744 | |||||||
| chr13:114269766 | G | A | 1 | a0001c0002t0009g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1604-2418G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269766 | |||||||
| chr13:114269789 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1604-2395C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269789 | |||||||
| chr13:114269939 | C | T | 1 | a0001c0008t0002g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1604-2245C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269939 | |||||||
| chr13:114269952 | C | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-2232C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269952 | |||||||
| chr13:114269953 | G | C | 1 | a0001c0002t0002g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1604-2231G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269953 | |||||||
| chr13:114269963 | C | T | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-2221C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269963 | |||||||
| chr13:114269993 | A | G | 1 | a0001c0001t0014g0115 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1604-2191A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114269993 | |||||||
| chr13:114270033 | G | A | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-2151G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270033 | |||||||
| chr13:114270039 | G | A | 1 | a0001c0002t0002g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1604-2145G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270039 | |||||||
| chr13:114270060 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1604-2124A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270060 | |||||||
| chr13:114270133 | A | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-2051A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270133 | |||||||
| chr13:114270220 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-1964T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270220 | |||||||
| chr13:114270229 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1604-1955T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270229 | |||||||
| chr13:114270365 | C | T | 2 | a0001c0002t0002g0195 a0001c0002t0002g0196 |
2 | HG00733.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1604-1819C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270365 | |||||||
| chr13:114270496 | C | T | 1 | a0001c0005t0006g0077 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1604-1688C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270496 | |||||||
| chr13:114270573 | G | A | 6 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1604-1611G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270573 | |||||||
| chr13:114270578 | G | GGGT | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-1605_1604-160 others(7): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114270578 | ||||||
| chr13:114270596 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-1588T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270596 | |||||||
| chr13:114270819 | T | C | 1 | a0001c0002t0002g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1604-1365T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270819 | |||||||
| chr13:114270869 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1604-1315A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270869 | |||||||
| chr13:114270894 | A | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(36): Show |
73 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1604-1290A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270894 | |||||||
| chr13:114270914 | C | CT | 27 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0033 others(24): Show |
41 | HG00140.hp2 HG00733.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.1604-1245dupT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114270914 | ||||||
| chr13:114270914 | C | CTT | 4 | a0001c0001t0001g0015 a0001c0001t0001g0124 a0001c0001t0001g0131 others(1): Show |
7 | NA18940.hp2 NA18947.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1604-1246_1604-124 others(6): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114270914 | ||||||
| chr13:114270914 | CT | C | 29 | a0001c0001t0001g0035 a0001c0001t0001g0082 a0001c0001t0001g0088 others(26): Show |
38 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1604-1245delT | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114270914 | ||||||
| chr13:114270914 | CTT | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-1246_1604-124 others(6): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114270914 | ||||||
| chr13:114270917 | T | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-1267T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270917 | |||||||
| chr13:114270925 | T | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-1259T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114270925 | |||||||
| chr13:114271071 | G | A | 6 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1604-1113G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271071 | |||||||
| chr13:114271075 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG01496.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1604-1109C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271075 | |||||||
| chr13:114271078 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-1106T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271078 | |||||||
| chr13:114271110 | A | C | 1 | a0001c0001t0001g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1604-1074A>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271110 | |||||||
| chr13:114271111 | C | G | 1 | a0001c0001t0001g0100 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1604-1073C>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271111 | |||||||
| chr13:114271125 | ATTAGCCA others(553): Show |
A | 1 | a0001c0001t0001g0036 | 2 | NA18957.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1604-1028_1604-469 others(3): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114271125 | ||||||
| chr13:114271164 | A | G | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-1020A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271164 | |||||||
| chr13:114271168 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0136 |
2 | HG00558.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1604-1016G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271168 | |||||||
| chr13:114271173 | G | A | 1 | a0001c0002t0002g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1604-1011G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271173 | |||||||
| chr13:114271222 | A | G | 1 | a0001c0002t0002g0050 | 2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1604-962A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271222 | |||||||
| chr13:114271290 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-894T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271290 | |||||||
| chr13:114271292 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-892T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271292 | |||||||
| chr13:114271380 | T | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-804T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271380 | |||||||
| chr13:114271483 | C | CTT | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-693_1604-692d others(4): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114271483 | ||||||
| chr13:114271527 | T | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01099.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1604-657T>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271527 | |||||||
| chr13:114271538 | T | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(174): Show |
292 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.1604-646T>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271538 | |||||||
| chr13:114271544 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1604-640G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271544 | |||||||
| chr13:114271651 | A | ATT | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-523_1604-522d others(4): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114271651 | ||||||
| chr13:114271670 | A | T | 6 | a0001c0003t0004g0021 a0001c0003t0004g0144 a0001c0003t0004g0145 others(3): Show |
8 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1604-514A>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271670 | |||||||
| chr13:114271728 | G | A | 1 | a0001c0002t0011g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1604-456G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271728 | |||||||
| chr13:114271790 | A | G | 1 | a0001c0009t0001g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1604-394A>G | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271790 | |||||||
| chr13:114271796 | T | TA | 1 | a0001c0003t0004g0021 | 3 | HG00735.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1604-387dupA | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr13 | 114271796 | ||||||
| chr13:114271878 | CTG | C | 1 | a0001c0002t0008g0019 | 3 | HG02258.hp2 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1604-305_1604-304d others(4): Show |
CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271878 | |||||||
| chr13:114271891 | T | C | 9 | a0001c0004t0003g0010 a0001c0004t0003g0030 a0001c0004t0003g0052 others(6): Show |
14 | HG00642.hp1 HG01361.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1604-293T>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271891 | |||||||
| chr13:114271902 | C | T | 1 | a0001c0002t0002g0053 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1604-282C>T | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114271902 | |||||||
| chr13:114272002 | G | C | 5 | a0001c0005t0005g0005 a0001c0005t0006g0020 a0001c0005t0006g0077 others(2): Show |
12 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1604-182G>C | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114272002 | |||||||
| chr13:114272138 | G | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(139): Show |
236 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1604-46G>A | CDC16 | ENSG00000130177.16 | transcript | ENST00000356221.8 | protein_coding | 17/17 | chr13 | 114272138 |