Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 899 |
| ensemblid | ENSG00000162063.13 |
| hgncid | 1591 |
| symbol | CCNF |
| name | cyclin F |
| refseq_nuc | NM_001761.3 |
| refseq_prot | NP_001752.2 |
| ensembl_nuc | ENST00000397066.9 |
| ensembl_prot | ENSP00000380256.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 2429447 |
| end | 2458854 |
| strand | + |
| ver | v1.2 |
| region | chr16:2429447-2458854 |
| region5000 | chr16:2424447-2463854 |
| regionname0 | CCNF_chr16_2429447_2458854 |
| regionname5000 | CCNF_chr16_2424447_2463854 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 786 | 270 | 86 | 56 | 76 | 12 | 38 | 53 | CCNF_chr16_2424447_2463854 | CCNF | MGSGG others(781): Show |
chr16 | 2424447 | 2463854 |
| a0002 | 0/0 | 786 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CCNF_chr16_2424447_2463854 | CCNF | MGSGG others(781): Show |
chr16 | 2424447 | 2463854 |
| a0003 | 0/0 | 786 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CCNF_chr16_2424447_2463854 | CCNF | MGSGG others(781): Show |
chr16 | 2424447 | 2463854 |
| a0004 | 0/0 | 786 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | MGSGG others(781): Show |
chr16 | 2424447 | 2463854 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2358 | 264 | 81 | 56 | 75 | 12 | 38 | CCNF_chr16_2424447_2463854 | CCNF | ATGGG others(2353): Show |
chr16 | 2424447 | 2463854 | ||
| a0001c0002 | 0/0 | 2358 | 4 | 4 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | ATGGG others(2353): Show |
chr16 | 2424447 | 2463854 | ||
| a0001c0006 | 0/0 | 2358 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | ATGGG others(2353): Show |
chr16 | 2424447 | 2463854 | ||
| a0001c0007 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | ATGGG others(2353): Show |
chr16 | 2424447 | 2463854 | ||
| a0002c0003 | 0/0 | 2358 | 3 | 0 | 0 | 3 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | ATGGG others(2353): Show |
chr16 | 2424447 | 2463854 | ||
| a0003c0004 | 0/0 | 2358 | 2 | 0 | 0 | 0 | 0 | 2 | CCNF_chr16_2424447_2463854 | CCNF | ATGGG others(2353): Show |
chr16 | 2424447 | 2463854 | ||
| a0004c0005 | 0/0 | 2358 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | ATGGG others(2353): Show |
chr16 | 2424447 | 2463854 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4230 | 233 | 60 | 50 | 72 | 12 | 37 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0001t0002 | 0/0 | 4230 | 13 | 12 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0001t0003 | 0/0 | 4229 | 5 | 0 | 3 | 2 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4224): Show |
chr16 | 2424447 | 2463854 |
| a0001c0001t0004 | 0/0 | 4230 | 4 | 4 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0001t0005 | 0/0 | 4230 | 2 | 2 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0001t0006 | 0/0 | 4230 | 2 | 2 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0001t0008 | 0/0 | 4230 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0001t0009 | 0/0 | 4230 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0001t0010 | 0/0 | 4230 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0001t0011 | 0/0 | 4230 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0001t0012 | 0/0 | 4230 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0002t0001 | 0/0 | 4230 | 2 | 2 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0002t0002 | 0/0 | 4230 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0002t0007 | 0/0 | 4230 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0006t0002 | 0/0 | 4230 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0001c0007t0001 | 0/0 | 4230 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0002c0003t0001 | 0/0 | 4230 | 3 | 0 | 0 | 3 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0003c0004t0001 | 0/0 | 4230 | 2 | 0 | 0 | 0 | 0 | 2 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| a0004c0005t0001 | 0/0 | 4230 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | AGGCG others(4225): Show |
chr16 | 2424447 | 2463854 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0028 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0010g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0001t0012g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0002t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0006t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0001c0007t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0002c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0002c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0003c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0003c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| a0004c0005t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | GBR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | FIN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01070 | hp1 | a0001 | c0001 | t0010 | g0053 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | IBS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01978 | hp2 | a0001 | c0001 | t0009 | g0196 | AMR | PEL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02080 | hp2 | a0004 | c0005 | t0001 | g0149 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CDX | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02630 | hp1 | a0001 | c0002 | t0007 | g0261 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0048 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02698 | hp2 | a0003 | c0004 | t0001 | g0057 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0226 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02738 | hp1 | a0003 | c0004 | t0001 | g0049 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0214 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0174 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0258 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0040 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ESN | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0259 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0243 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18991 | hp1 | a0001 | c0007 | t0001 | g0146 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18994 | hp1 | a0001 | c0001 | t0012 | g0058 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19064 | hp1 | a0002 | c0003 | t0001 | g0035 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19065 | hp1 | a0002 | c0003 | t0001 | g0143 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | YRI | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | YRI | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ASW | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | ASW | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG06807 | hp1 | a0001 | c0006 | t0002 | g0131 | AFR | USA | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | USA | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | USA | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | USA | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0153 | REF | REF | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0028 | REF | REF | CCNF_chr16_2424447_2463854 | CCNF | chr16 | 2424447 | 2463854 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:2433009 | G | A | 1 | a0003 | 2 | HG02698.hp2 HG02738.hp1 |
missense_variant | MODERATE | c.220G>A | p.Ala74Thr | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/17 | 255/4230 | 220/2361 | 74/786 | chr16 | 2433009 | |||
| chr16:2453414 | T | G | 1 | a0004 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1592T>G | p.Leu531Arg | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/17 | 1627/4230 | 1592/2361 | 531/786 | chr16 | 2453414 | |||
| chr16:2455489 | T | A | 1 | a0002 | 3 | NA18964.hp2 NA19064.hp1 NA19065.hp1 |
missense_variant | MODERATE | c.1810T>A | p.Phe604Ile | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/17 | 1845/4230 | 1810/2361 | 604/786 | chr16 | 2455489 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:2437217 | C | T | 1 | a0001c0007 | 1 | NA18991.hp1 | synonymous_variant | LOW | c.435C>T | p.Ala145Ala | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/17 | 470/4230 | 435/2361 | 145/786 | chr16 | 2437217 | |||
| chr16:2449455 | C | T | 1 | a0001c0006 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1392C>T | p.His464His | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 12/17 | 1427/4230 | 1392/2361 | 464/786 | chr16 | 2449455 | |||
| chr16:2456861 | G | A | 1 | a0001c0002 | 4 | HG02451.hp2 HG02630.hp1 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.2202G>A | p.Ser734Ser | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 17/17 | 2237/4230 | 2202/2361 | 734/786 | chr16 | 2456861 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:2429481 | G | C | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(2): Show |
20 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-1G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/17 | 1 | chr16 | 2429481 | ||||||
| chr16:2457311 | G | A | 1 | a0001c0001t0004 | 4 | HG02922.hp2 HG02970.hp1 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*291G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 17/17 | 291 | chr16 | 2457311 | ||||||
| chr16:2457462 | G | A | 1 | a0001c0001t0005 | 2 | HG02647.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*442G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 17/17 | 442 | chr16 | 2457462 | ||||||
| chr16:2457521 | C | T | 1 | a0001c0002t0007 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 17/17 | 501 | chr16 | 2457521 | ||||||
| chr16:2457616 | C | T | 1 | a0001c0001t0012 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*596C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 17/17 | 596 | chr16 | 2457616 | ||||||
| chr16:2457653 | C | T | 1 | a0001c0001t0011 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*633C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 17/17 | 633 | chr16 | 2457653 | ||||||
| chr16:2457669 | A | G | 1 | a0001c0001t0010 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 17/17 | 649 | chr16 | 2457669 | ||||||
| chr16:2457767 | A | G | 1 | a0001c0001t0009 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*747A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 17/17 | 747 | chr16 | 2457767 | ||||||
| chr16:2457897 | C | G | 2 | a0001c0001t0004 a0001c0001t0006 |
6 | HG02896.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*877C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 17/17 | 877 | chr16 | 2457897 | ||||||
| chr16:2458020 | C | A | 1 | a0001c0001t0008 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1000C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 17/17 | 1000 | chr16 | 2458020 | ||||||
| chr16:2458253 | CT | C | 1 | a0001c0001t0003 | 5 | HG01167.hp1 HG01257.hp1 HG01975.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1251delT | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 17/17 | 1251 | INFO_REALIGN_3_PRIME | chr16 | 2458253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:2429506 | G | T | 1 | a0001c0001t0001g0262 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.16+9G>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2429506 | |||||||
| chr16:2429711 | A | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.16+214A>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2429711 | |||||||
| chr16:2429717 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.16+220C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2429717 | |||||||
| chr16:2429772 | AGCGATCC others(20): Show |
A | 19 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0249 others(16): Show |
19 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.16+282_16+308delCG others(25): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 2429772 | ||||||
| chr16:2429785 | TCGGGTCC others(5): Show |
T | 1 | a0001c0001t0001g0162 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.16+292_16+303delGT others(10): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 2429785 | ||||||
| chr16:2429792 | CCGGGGCG others(12): Show |
C | 1 | a0001c0001t0011g0214 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.16+301_16+319delCG others(17): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr16 | 2429792 | ||||||
| chr16:2429998 | C | T | 1 | a0001c0002t0007g0261 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.16+501C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2429998 | |||||||
| chr16:2430079 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 |
3 | HG01081.hp2 HG01496.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.16+582G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2430079 | |||||||
| chr16:2430176 | C | G | 3 | a0001c0001t0002g0260 a0001c0002t0002g0259 a0001c0002t0007g0261 |
3 | HG02630.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.16+679C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2430176 | |||||||
| chr16:2430428 | G | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0060 others(61): Show |
66 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.17-702G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2430428 | |||||||
| chr16:2430442 | G | A | 10 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(7): Show |
10 | HG01069.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.17-688G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2430442 | |||||||
| chr16:2430473 | T | C | 5 | a0001c0001t0002g0246 a0001c0001t0004g0243 a0001c0001t0004g0244 others(2): Show |
5 | HG02559.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.17-657T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2430473 | |||||||
| chr16:2430784 | A | T | 1 | a0001c0001t0001g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.17-346A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2430784 | |||||||
| chr16:2430820 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.17-310C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2430820 | |||||||
| chr16:2430947 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(12): Show |
18 | HG00741.hp1 HG01070.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-183A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2430947 | |||||||
| chr16:2431103 | C | G | 18 | a0001c0001t0002g0246 a0001c0001t0002g0249 a0001c0001t0002g0250 others(15): Show |
18 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-27C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 1/16 | chr16 | 2431103 | |||||||
| chr16:2431406 | C | T | 1 | a0001c0001t0004g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.171+122C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | chr16 | 2431406 | |||||||
| chr16:2431600 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.171+316A>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | chr16 | 2431600 | |||||||
| chr16:2431679 | C | CA | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(6): Show |
9 | HG01109.hp1 HG02615.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+414dupA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 2431679 | ||||||
| chr16:2431679 | CA | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.171+414delA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 2431679 | ||||||
| chr16:2431775 | C | T | 19 | a0001c0001t0002g0246 a0001c0001t0002g0249 a0001c0001t0002g0250 others(16): Show |
19 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.171+491C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | chr16 | 2431775 | |||||||
| chr16:2431836 | C | CT | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.171+564dupT | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 2431836 | ||||||
| chr16:2431836 | C | CTT | 6 | a0001c0001t0002g0246 a0001c0001t0002g0260 a0001c0001t0004g0243 others(3): Show |
6 | HG02559.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+563_171+564dup others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr16 | 2431836 | ||||||
| chr16:2431899 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.171+615C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | chr16 | 2431899 | |||||||
| chr16:2432081 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.171+797C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | chr16 | 2432081 | |||||||
| chr16:2432148 | C | T | 6 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(3): Show |
6 | HG00639.hp2 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.172-813C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | chr16 | 2432148 | |||||||
| chr16:2432163 | C | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0047 |
2 | NA18943.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.172-798C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | chr16 | 2432163 | |||||||
| chr16:2432338 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.172-623C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | chr16 | 2432338 | |||||||
| chr16:2432452 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.172-509T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | chr16 | 2432452 | |||||||
| chr16:2432551 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.172-410G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 2/16 | chr16 | 2432551 | |||||||
| chr16:2433179 | T | C | 10 | a0001c0001t0002g0248 a0001c0001t0002g0250 a0001c0001t0002g0251 others(7): Show |
10 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.278+112T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2433179 | |||||||
| chr16:2433507 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.278+440C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2433507 | |||||||
| chr16:2433607 | A | G | 1 | a0003c0004t0001g0057 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.278+540A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2433607 | |||||||
| chr16:2433618 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0120 |
2 | NA18949.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.278+551C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2433618 | |||||||
| chr16:2433630 | A | T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.278+563A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2433630 | |||||||
| chr16:2433631 | G | T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.278+564G>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2433631 | |||||||
| chr16:2433648 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.278+581G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2433648 | |||||||
| chr16:2433649 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.278+582C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2433649 | |||||||
| chr16:2433743 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.278+676G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2433743 | |||||||
| chr16:2433844 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.278+777G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2433844 | |||||||
| chr16:2433885 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.278+818A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2433885 | |||||||
| chr16:2434169 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.278+1102G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434169 | |||||||
| chr16:2434345 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.278+1278T>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434345 | |||||||
| chr16:2434352 | C | T | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.278+1285C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434352 | |||||||
| chr16:2434546 | G | C | 19 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0249 others(16): Show |
19 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.279-1260G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434546 | |||||||
| chr16:2434565 | C | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | HG02886.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.279-1241C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434565 | |||||||
| chr16:2434597 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.279-1209C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434597 | |||||||
| chr16:2434606 | G | A | 9 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0144 others(6): Show |
9 | HG00438.hp2 HG02040.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.279-1200G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434606 | |||||||
| chr16:2434680 | T | C | 1 | a0001c0001t0005g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.279-1126T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434680 | |||||||
| chr16:2434743 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.279-1063C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434743 | |||||||
| chr16:2434782 | A | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.279-1024A>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434782 | |||||||
| chr16:2434831 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.279-975G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434831 | |||||||
| chr16:2434850 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.279-956T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434850 | |||||||
| chr16:2434976 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.279-830C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2434976 | |||||||
| chr16:2435020 | C | T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.279-786C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435020 | |||||||
| chr16:2435067 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.279-739T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435067 | |||||||
| chr16:2435144 | G | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.279-662G>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435144 | |||||||
| chr16:2435159 | G | C | 1 | a0001c0002t0007g0261 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.279-647G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435159 | |||||||
| chr16:2435167 | T | C | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.279-639T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435167 | |||||||
| chr16:2435191 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.279-615T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435191 | |||||||
| chr16:2435229 | C | T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.279-577C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435229 | |||||||
| chr16:2435249 | C | CA | 7 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
7 | HG01169.hp2 HG02109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.279-545dupA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435249 | ||||||
| chr16:2435261 | AG | A | 4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0137 others(1): Show |
4 | HG02165.hp1 HG02523.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.279-544delG | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435261 | |||||||
| chr16:2435262 | G | A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(205): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.279-544G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435262 | |||||||
| chr16:2435280 | A | G | 16 | a0001c0001t0001g0010 a0001c0001t0001g0136 a0001c0001t0001g0151 others(13): Show |
17 | HG00735.hp2 HG01167.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.279-526A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435280 | |||||||
| chr16:2435303 | C | T | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.279-503C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435303 | |||||||
| chr16:2435424 | A | AT | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.279-373dupT | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435424 | ||||||
| chr16:2435458 | G | A | 10 | a0001c0001t0002g0248 a0001c0001t0002g0250 a0001c0001t0002g0251 others(7): Show |
10 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.279-348G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435458 | |||||||
| chr16:2435510 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.279-296A>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435510 | |||||||
| chr16:2435576 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.279-230C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435576 | |||||||
| chr16:2435588 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.279-218G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435588 | |||||||
| chr16:2435596 | GAT | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(205): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.279-195_279-194del others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435596 | ||||||
| chr16:2435598 | T | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0070 a0001c0001t0001g0117 others(1): Show |
4 | HG01169.hp2 HG02602.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.279-208T>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435598 | |||||||
| chr16:2435600 | T | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(173): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.279-206T>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435600 | |||||||
| chr16:2435602 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.279-204T>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435602 | |||||||
| chr16:2435611 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0117 |
2 | HG01169.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.279-195A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435611 | |||||||
| chr16:2435612 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0117 |
2 | HG01169.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.279-194T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435612 | |||||||
| chr16:2435613 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0117 |
2 | HG01169.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.279-193G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435613 | |||||||
| chr16:2435628 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.279-178C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435628 | |||||||
| chr16:2435640 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.279-166C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435640 | |||||||
| chr16:2435644 | CATATATA others(23): Show |
C | 10 | a0001c0001t0002g0248 a0001c0001t0002g0250 a0001c0001t0002g0251 others(7): Show |
10 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.279-151_279-122del others(30): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435644 | ||||||
| chr16:2435644 | CATATATA others(25): Show |
C | 9 | a0001c0001t0001g0068 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
9 | HG01433.hp1 HG02523.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.279-151_279-120del others(32): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435644 | ||||||
| chr16:2435644 | CATATATA others(27): Show |
C | 51 | a0001c0001t0001g0010 a0001c0001t0001g0063 a0001c0001t0001g0070 others(48): Show |
52 | HG00280.hp2 HG00597.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.279-151_279-118del others(34): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435644 | ||||||
| chr16:2435644 | CATATATA others(29): Show |
C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(131): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.279-151_279-116del others(36): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435644 | ||||||
| chr16:2435644 | CATATATA others(31): Show |
C | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0204 others(2): Show |
5 | HG02809.hp1 HG03579.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.279-151_279-114del others(38): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435644 | ||||||
| chr16:2435644 | CATATATA others(33): Show |
C | 2 | a0001c0001t0002g0246 a0001c0006t0002g0131 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.279-151_279-112del others(40): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435644 | ||||||
| chr16:2435662 | CACACATA others(9): Show |
C | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.279-142_279-127del others(16): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435662 | ||||||
| chr16:2435664 | CACATATA others(7): Show |
C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | NA18941.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.279-140_279-127del others(14): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435664 | ||||||
| chr16:2435664 | CACATATA others(9): Show |
C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0019 others(7): Show |
11 | HG00738.hp1 HG02523.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.279-140_279-125del others(16): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435664 | ||||||
| chr16:2435666 | C | CATAT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0037 others(2): Show |
6 | HG00735.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.279-105_279-102dup others(4): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435666 | ||||||
| chr16:2435666 | C | CATATAT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0002c0003t0001g0035 |
3 | HG02080.hp1 HG02602.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.279-107_279-102dup others(6): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435666 | ||||||
| chr16:2435666 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0036 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.279-111_279-102dup others(10): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435666 | ||||||
| chr16:2435666 | CAT | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0030 others(7): Show |
10 | HG00642.hp2 HG01099.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.279-103_279-102del others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435666 | ||||||
| chr16:2435666 | CATAT | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0047 others(1): Show |
4 | HG00741.hp1 HG01433.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.279-105_279-102del others(4): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr16 | 2435666 | ||||||
| chr16:2435668 | T | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
6 | HG01081.hp2 HG01257.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.279-138T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435668 | |||||||
| chr16:2435676 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0010g0053 |
2 | HG01070.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.279-130T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435676 | |||||||
| chr16:2435678 | T | C | 6 | a0001c0001t0001g0068 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG01433.hp1 HG02523.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.279-128T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435678 | |||||||
| chr16:2435680 | T | C | 50 | a0001c0001t0001g0010 a0001c0001t0001g0063 a0001c0001t0001g0070 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.279-126T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435680 | |||||||
| chr16:2435682 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.279-124T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435682 | |||||||
| chr16:2435682 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(126): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.279-124T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435682 | |||||||
| chr16:2435684 | T | C | 7 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0133 others(4): Show |
7 | HG02132.hp1 HG02165.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.279-122T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435684 | |||||||
| chr16:2435718 | C | G | 2 | a0001c0001t0001g0041 a0001c0001t0006g0040 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.279-88C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435718 | |||||||
| chr16:2435748 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.279-58T>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 3/16 | chr16 | 2435748 | |||||||
| chr16:2435895 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.346+22A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2435895 | |||||||
| chr16:2436102 | C | G | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.346+229C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2436102 | |||||||
| chr16:2436181 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.346+308A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2436181 | |||||||
| chr16:2436189 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.346+316G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2436189 | |||||||
| chr16:2436289 | C | T | 1 | a0001c0001t0012g0058 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.346+416C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2436289 | |||||||
| chr16:2436382 | C | A | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.346+509C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2436382 | |||||||
| chr16:2436463 | T | C | 1 | a0001c0001t0003g0075 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.346+590T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2436463 | |||||||
| chr16:2436494 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.346+621A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2436494 | |||||||
| chr16:2436535 | C | G | 1 | a0002c0003t0001g0039 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.347-594C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2436535 | |||||||
| chr16:2436614 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.347-515C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2436614 | |||||||
| chr16:2436934 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.347-195C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2436934 | |||||||
| chr16:2436997 | A | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.347-132A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2436997 | |||||||
| chr16:2437011 | C | CT | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.347-118_347-117ins others(1): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2437011 | |||||||
| chr16:2437049 | T | A | 1 | a0001c0001t0001g0223 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.347-80T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 4/16 | chr16 | 2437049 | |||||||
| chr16:2437419 | G | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(185): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.540+97G>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | chr16 | 2437419 | |||||||
| chr16:2437437 | G | C | 1 | a0001c0001t0004g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.540+115G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | chr16 | 2437437 | |||||||
| chr16:2437470 | C | G | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.540+148C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | chr16 | 2437470 | |||||||
| chr16:2437483 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.540+161C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | chr16 | 2437483 | |||||||
| chr16:2437542 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.540+220G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | chr16 | 2437542 | |||||||
| chr16:2437545 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.540+223C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | chr16 | 2437545 | |||||||
| chr16:2437667 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.540+345T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | chr16 | 2437667 | |||||||
| chr16:2437792 | A | G | 19 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0249 others(16): Show |
19 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.541-278A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | chr16 | 2437792 | |||||||
| chr16:2437852 | C | CTA | 2 | a0001c0001t0001g0001 a0001c0001t0001g0052 |
5 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-216_541-215dup others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 2437852 | ||||||
| chr16:2437891 | C | G | 1 | a0001c0001t0001g0116 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.541-179C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | chr16 | 2437891 | |||||||
| chr16:2437903 | T | TA | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(186): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.541-148dupA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 2437903 | ||||||
| chr16:2437903 | T | TAA | 13 | a0001c0001t0001g0076 a0001c0001t0002g0248 a0001c0001t0002g0250 others(10): Show |
13 | HG00621.hp2 HG01346.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-149_541-148dup others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr16 | 2437903 | ||||||
| chr16:2438176 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.594+53C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 6/16 | chr16 | 2438176 | |||||||
| chr16:2438210 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.594+87T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 6/16 | chr16 | 2438210 | |||||||
| chr16:2438318 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.594+195C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 6/16 | chr16 | 2438318 | |||||||
| chr16:2438642 | G | GA | 6 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0056 others(3): Show |
6 | HG01109.hp1 HG03942.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.594+534dupA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr16 | 2438642 | ||||||
| chr16:2438692 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.594+569T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 6/16 | chr16 | 2438692 | |||||||
| chr16:2438825 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.595-528C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 6/16 | chr16 | 2438825 | |||||||
| chr16:2438902 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.595-451G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 6/16 | chr16 | 2438902 | |||||||
| chr16:2439071 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.595-282G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 6/16 | chr16 | 2439071 | |||||||
| chr16:2439105 | C | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(188): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.595-248C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 6/16 | chr16 | 2439105 | |||||||
| chr16:2439327 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0242 |
2 | HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.595-26A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 6/16 | chr16 | 2439327 | |||||||
| chr16:2439506 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.699+49G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 7/16 | chr16 | 2439506 | |||||||
| chr16:2439532 | T | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.699+75T>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 7/16 | chr16 | 2439532 | |||||||
| chr16:2439835 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.777+9C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2439835 | |||||||
| chr16:2439907 | T | A | 6 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+81T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2439907 | |||||||
| chr16:2439910 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.777+84G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2439910 | |||||||
| chr16:2439969 | C | T | 10 | a0001c0001t0002g0248 a0001c0001t0002g0250 a0001c0001t0002g0251 others(7): Show |
10 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.777+143C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2439969 | |||||||
| chr16:2440131 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.777+305T>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2440131 | |||||||
| chr16:2440132 | G | C | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.777+306G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2440132 | |||||||
| chr16:2440229 | G | C | 1 | a0001c0001t0001g0062 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.777+403G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2440229 | |||||||
| chr16:2440255 | T | G | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.777+429T>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2440255 | |||||||
| chr16:2440393 | C | T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.777+567C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2440393 | |||||||
| chr16:2440488 | G | C | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.777+662G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2440488 | |||||||
| chr16:2440505 | A | ACC | 4 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(1): Show |
4 | HG01169.hp2 HG02602.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+679_777+680ins others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2440505 | |||||||
| chr16:2440592 | C | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0022 others(5): Show |
9 | HG02523.hp2 NA18941.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.777+766C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2440592 | |||||||
| chr16:2440634 | C | T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.777+808C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2440634 | |||||||
| chr16:2440868 | C | T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.777+1042C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2440868 | |||||||
| chr16:2440922 | C | T | 2 | a0001c0001t0005g0048 a0001c0001t0005g0150 |
2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.777+1096C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2440922 | |||||||
| chr16:2441077 | C | CA | 5 | a0001c0001t0002g0246 a0001c0001t0004g0243 a0001c0001t0004g0244 others(2): Show |
5 | HG02559.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+1258dupA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441077 | ||||||
| chr16:2441174 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.777+1348C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441174 | |||||||
| chr16:2441224 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.777+1398C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441224 | |||||||
| chr16:2441244 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.777+1418A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441244 | |||||||
| chr16:2441264 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.777+1438C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441264 | |||||||
| chr16:2441306 | G | C | 1 | a0001c0001t0005g0048 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.777+1480G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441306 | |||||||
| chr16:2441322 | C | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.777+1496C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441322 | |||||||
| chr16:2441615 | C | A | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.777+1789C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441615 | |||||||
| chr16:2441623 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+1797G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441623 | |||||||
| chr16:2441628 | G | T | 1 | a0001c0001t0001g0068 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.777+1802G>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441628 | |||||||
| chr16:2441746 | A | C | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.778-1903A>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441746 | |||||||
| chr16:2441781 | T | G | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.778-1868T>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441781 | |||||||
| chr16:2441785 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.778-1864G>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441785 | |||||||
| chr16:2441935 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.778-1714A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441935 | |||||||
| chr16:2441936 | A | T | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.778-1713A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441936 | |||||||
| chr16:2441937 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.778-1712T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441937 | |||||||
| chr16:2441937 | T | TTA | 32 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0073 others(29): Show |
34 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.778-1668_778-1667d others(4): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | T | TTATA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0042 others(38): Show |
43 | HG00280.hp2 HG00642.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.778-1670_778-1667d others(6): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | T | TTATATA | 16 | a0001c0001t0001g0062 a0001c0001t0001g0082 a0001c0001t0001g0083 others(13): Show |
16 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.778-1672_778-1667d others(8): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | T | TTATATAT others(1): Show |
11 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0074 others(8): Show |
11 | HG00597.hp2 HG00621.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.778-1674_778-1667d others(10): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | T | TTATATAT others(3): Show |
7 | a0001c0001t0001g0059 a0001c0001t0001g0078 a0001c0001t0001g0079 others(4): Show |
7 | HG01261.hp1 HG02056.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-1676_778-1667d others(12): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.778-1678_778-1667d others(14): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0067 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.778-1680_778-1667d others(16): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTA | T | 12 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0113 others(9): Show |
12 | HG00639.hp1 HG02293.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.778-1668_778-1667d others(4): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTATA | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0029 others(8): Show |
11 | HG01099.hp1 HG02165.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.778-1670_778-1667d others(6): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTATATA | T | 5 | a0001c0001t0001g0125 a0001c0001t0001g0168 a0001c0001t0001g0218 others(2): Show |
5 | HG02040.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-1672_778-1667d others(8): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTATATAT others(1): Show |
T | 11 | a0001c0001t0001g0041 a0001c0001t0001g0121 a0001c0001t0001g0126 others(8): Show |
11 | HG01070.hp1 HG01243.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.778-1674_778-1667d others(10): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTATATAT others(3): Show |
T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(13): Show |
19 | HG00741.hp1 HG01081.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.778-1676_778-1667d others(12): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTATATAT others(5): Show |
T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(28): Show |
34 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.778-1678_778-1667d others(14): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTATATAT others(7): Show |
T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0047 |
2 | HG03927.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.778-1680_778-1667d others(16): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTATATAT others(9): Show |
T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0221 a0001c0001t0002g0256 |
3 | HG01346.hp2 HG02257.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.778-1682_778-1667d others(18): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTATATAT others(11): Show |
T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0136 a0001c0001t0001g0151 others(13): Show |
17 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.778-1684_778-1667d others(20): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTATATAT others(13): Show |
T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0239 a0001c0001t0001g0262 others(1): Show |
4 | HG00639.hp2 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-1686_778-1667d others(22): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTATATAT others(15): Show |
T | 1 | a0001c0001t0001g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.778-1688_778-1667d others(24): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441937 | TTATATAT others(19): Show |
T | 1 | a0001c0001t0001g0076 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.778-1692_778-1667d others(28): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441937 | ||||||
| chr16:2441939 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.778-1710A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441939 | |||||||
| chr16:2441949 | ATATATAT others(31): Show |
A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.778-1698_778-1661d others(40): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441949 | ||||||
| chr16:2441981 | A | ATATATAT others(9): Show |
1 | a0001c0002t0007g0261 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.778-1667_778-1666i others(18): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441981 | ||||||
| chr16:2441981 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.778-1668A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2441981 | |||||||
| chr16:2441990 | TTTTTGTT others(3): Show |
T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.778-1634_778-1625d others(12): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2441990 | ||||||
| chr16:2442028 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.778-1621T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442028 | |||||||
| chr16:2442039 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.778-1610T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442039 | |||||||
| chr16:2442082 | C | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.778-1567C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442082 | |||||||
| chr16:2442359 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.778-1290A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442359 | |||||||
| chr16:2442398 | T | TTATAATA others(215): Show |
1 | a0001c0001t0006g0040 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.778-1033_778-1032i others(224): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442398 | ||||||
| chr16:2442406 | TATAATAT others(215): Show |
T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0129 |
3 | HG02630.hp2 HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.778-1239_778-1018d others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442406 | ||||||
| chr16:2442423 | TAATATTA others(241): Show |
T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.778-1225_778-978de others(1): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442423 | |||||||
| chr16:2442426 | TATTA | T | 10 | a0001c0001t0002g0248 a0001c0001t0002g0250 a0001c0001t0002g0251 others(7): Show |
10 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.778-1222_778-1219d others(6): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442426 | |||||||
| chr16:2442429 | TATTATAT others(222): Show |
T | 1 | a0001c0001t0002g0246 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.778-1217_778-989de others(1): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442429 | ||||||
| chr16:2442430 | AT | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(181): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.778-1217delT | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442430 | ||||||
| chr16:2442431 | T | TA | 3 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0009g0196 |
3 | HG00544.hp2 HG01978.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.778-1218_778-1217i others(3): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442431 | |||||||
| chr16:2442432 | T | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0088 others(6): Show |
9 | HG02572.hp2 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-1217T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442432 | |||||||
| chr16:2442433 | A | T | 9 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0088 others(6): Show |
9 | HG02572.hp2 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-1216A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442433 | |||||||
| chr16:2442434 | T | A | 9 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0088 others(6): Show |
9 | HG02572.hp2 HG02809.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-1215T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442434 | |||||||
| chr16:2442434 | T | TA | 3 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0009g0196 |
3 | HG00544.hp2 HG01978.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.778-1214dupA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442434 | ||||||
| chr16:2442435 | ATATAATA others(174): Show |
A | 3 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 |
3 | HG02922.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.778-1213_778-1033d others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442435 | |||||||
| chr16:2442435 | ATATAATA others(211): Show |
A | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(178): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.778-1213_778-996de others(1): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442435 | |||||||
| chr16:2442437 | ATAATATA others(209): Show |
A | 10 | a0001c0001t0002g0248 a0001c0001t0002g0250 a0001c0001t0002g0251 others(7): Show |
10 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.778-1211_778-996de others(1): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442437 | |||||||
| chr16:2442438 | T | A | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.778-1211T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442438 | |||||||
| chr16:2442439 | A | T | 13 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG00544.hp2 HG01978.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.778-1210A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442439 | |||||||
| chr16:2442453 | TATA | T | 7 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0179 others(4): Show |
7 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-1192_778-1190d others(5): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442453 | ||||||
| chr16:2442453 | TATAATAT others(178): Show |
T | 1 | a0001c0001t0001g0204 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.778-1192_778-1008d others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442453 | ||||||
| chr16:2442455 | TAATATAA others(181): Show |
T | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.778-1192_778-1005d others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442455 | ||||||
| chr16:2442455 | TAATATAA others(220): Show |
T | 1 | a0001c0001t0001g0083 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.778-1192_778-966de others(1): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442455 | ||||||
| chr16:2442461 | A | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0009g0196 |
3 | HG00544.hp2 HG01978.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.778-1188A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442461 | |||||||
| chr16:2442462 | ATATTATT others(217): Show |
A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0009g0196 |
3 | HG00544.hp2 HG01978.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.778-1180_778-957de others(1): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442462 | ||||||
| chr16:2442465 | TTATTATA others(182): Show |
T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0088 |
2 | HG03017.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.778-1180_778-992de others(1): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442465 | ||||||
| chr16:2442466 | TATTATAT others(185): Show |
T | 4 | a0001c0001t0001g0179 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
4 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-1180_778-989de others(1): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442466 | ||||||
| chr16:2442476 | A | T | 1 | a0001c0001t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.778-1173A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442476 | |||||||
| chr16:2442500 | TATTATTA others(191): Show |
T | 1 | a0001c0001t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.778-1143_778-946de others(1): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442500 | ||||||
| chr16:2442531 | A | T | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.778-1118A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442531 | |||||||
| chr16:2442568 | A | T | 1 | a0001c0001t0001g0033 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.778-1081A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442568 | |||||||
| chr16:2442576 | TTATTATA others(27): Show |
T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0002c0003t0001g0035 others(1): Show |
4 | HG02165.hp2 NA18964.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-1032_778-999de others(35): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442576 | ||||||
| chr16:2442594 | A | AAT | 2 | a0003c0004t0001g0049 a0003c0004t0001g0057 |
2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.778-1052_778-1051d others(4): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442594 | ||||||
| chr16:2442599 | T | A | 2 | a0003c0004t0001g0049 a0003c0004t0001g0057 |
2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.778-1050T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442599 | |||||||
| chr16:2442610 | A | ATAT | 19 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(16): Show |
19 | HG00738.hp1 HG01070.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.778-1035_778-1033d others(5): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442610 | ||||||
| chr16:2442610 | A | ATATTATT others(33): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(10): Show |
15 | HG00544.hp1 HG00741.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.778-1033_778-1032i others(42): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442610 | ||||||
| chr16:2442610 | A | ATATTATT others(70): Show |
8 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
8 | HG00735.hp1 HG01109.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.778-1033_778-1032i others(79): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442610 | ||||||
| chr16:2442610 | A | ATATTATT others(107): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0044 others(1): Show |
4 | HG00642.hp2 HG01099.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-1033_778-1032i others(116): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442610 | ||||||
| chr16:2442610 | A | ATATTATT others(144): Show |
1 | a0001c0001t0001g0054 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.778-1033_778-1032i others(153): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442610 | ||||||
| chr16:2442610 | A | ATATTATT others(218): Show |
1 | a0001c0001t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.778-1033_778-1032i others(227): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442610 | ||||||
| chr16:2442621 | A | T | 3 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 |
3 | HG02922.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.778-1028A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442621 | |||||||
| chr16:2442647 | T | A | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.778-1002T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442647 | |||||||
| chr16:2442651 | T | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0129 others(4): Show |
7 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-998T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442651 | |||||||
| chr16:2442652 | A | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0129 others(4): Show |
7 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-997A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442652 | |||||||
| chr16:2442653 | T | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0129 others(4): Show |
7 | HG02630.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-996T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442653 | |||||||
| chr16:2442657 | T | A | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.778-992T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442657 | |||||||
| chr16:2442658 | A | T | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(196): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.778-991A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442658 | |||||||
| chr16:2442659 | A | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0088 |
2 | HG03017.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.778-990A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442659 | |||||||
| chr16:2442671 | A | ATATAATA others(28): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0051 |
2 | NA19005.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.778-974_778-973ins others(35): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442671 | ||||||
| chr16:2442678 | A | T | 19 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0249 others(16): Show |
19 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.778-971A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442678 | |||||||
| chr16:2442680 | ATCATAT | A | 19 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0249 others(16): Show |
19 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.778-967_778-962del others(6): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442680 | ||||||
| chr16:2442682 | C | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.778-967C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442682 | |||||||
| chr16:2442682 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(185): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.778-967C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442682 | |||||||
| chr16:2442683 | ATAT | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(185): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.778-959_778-957del others(3): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442683 | ||||||
| chr16:2442686 | T | A | 1 | a0001c0001t0001g0083 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.778-963T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442686 | |||||||
| chr16:2442697 | TA | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.778-950delA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442697 | ||||||
| chr16:2442710 | A | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0106 a0001c0001t0001g0116 |
3 | NA18984.hp1 NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.778-939A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442710 | |||||||
| chr16:2442711 | T | A | 3 | a0001c0001t0001g0086 a0001c0001t0001g0106 a0001c0001t0001g0116 |
3 | NA18984.hp1 NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.778-938T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442711 | |||||||
| chr16:2442712 | A | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0106 a0001c0001t0001g0116 |
3 | NA18984.hp1 NA18985.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.778-937A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442712 | |||||||
| chr16:2442714 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.778-935G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442714 | |||||||
| chr16:2442733 | CAT | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(188): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.778-912_778-911del others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442733 | ||||||
| chr16:2442751 | T | TTATAA | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.778-895_778-891dup others(5): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442751 | ||||||
| chr16:2442752 | TATA | T | 5 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 others(2): Show |
5 | HG02896.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-890_778-888del others(3): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442752 | ||||||
| chr16:2442766 | ATATATCA others(1): Show |
A | 5 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 others(2): Show |
5 | HG02896.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-882_778-875del others(8): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442766 | |||||||
| chr16:2442772 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.778-877C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442772 | |||||||
| chr16:2442775 | ATATAATA others(15): Show |
A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(188): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.778-865_778-844del others(22): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442775 | ||||||
| chr16:2442780 | ATAT | A | 21 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0249 others(18): Show |
21 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.778-865_778-863del others(3): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442780 | ||||||
| chr16:2442790 | TTATATTC others(12): Show |
T | 16 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0249 others(13): Show |
16 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.778-841_778-823del others(19): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442790 | ||||||
| chr16:2442791 | T | C | 5 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 others(2): Show |
5 | HG02896.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-858T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442791 | |||||||
| chr16:2442794 | ATTC | A | 5 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 others(2): Show |
5 | HG02896.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-853_778-851del others(3): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442794 | ||||||
| chr16:2442808 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.778-841A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442808 | |||||||
| chr16:2442809 | A | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(193): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.778-840A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442809 | |||||||
| chr16:2442880 | A | G | 1 | a0001c0001t0002g0258 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.778-769A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442880 | |||||||
| chr16:2442889 | T | TA | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.778-759dupA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442889 | ||||||
| chr16:2442903 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.778-746T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442903 | |||||||
| chr16:2442915 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-734A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442915 | |||||||
| chr16:2442922 | A | T | 1 | a0001c0001t0001g0027 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.778-727A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442922 | |||||||
| chr16:2442931 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.778-718G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442931 | |||||||
| chr16:2442937 | T | TATATA | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.778-711_778-707dup others(5): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2442937 | ||||||
| chr16:2442943 | T | A | 10 | a0001c0001t0002g0248 a0001c0001t0002g0250 a0001c0001t0002g0251 others(7): Show |
10 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.778-706T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442943 | |||||||
| chr16:2442950 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.778-699A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442950 | |||||||
| chr16:2442959 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.778-690T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442959 | |||||||
| chr16:2442975 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.778-674A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2442975 | |||||||
| chr16:2443009 | AATTAT | A | 6 | a0001c0001t0001g0135 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.778-632_778-628del others(5): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2443009 | ||||||
| chr16:2443098 | T | TA | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.778-551_778-550ins others(1): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443098 | |||||||
| chr16:2443122 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.778-527T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443122 | |||||||
| chr16:2443158 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.778-491A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443158 | |||||||
| chr16:2443160 | T | A | 1 | a0001c0001t0001g0027 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.778-489T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443160 | |||||||
| chr16:2443160 | TATATATA others(11): Show |
T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.778-470_778-453del others(18): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2443160 | ||||||
| chr16:2443161 | A | T | 1 | a0001c0001t0001g0027 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.778-488A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443161 | |||||||
| chr16:2443171 | TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0086 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.778-470_778-457del others(14): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr16 | 2443171 | ||||||
| chr16:2443180 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.778-469T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443180 | |||||||
| chr16:2443189 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.778-460T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443189 | |||||||
| chr16:2443286 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.778-363G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443286 | |||||||
| chr16:2443412 | C | T | 1 | a0001c0001t0004g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.778-237C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443412 | |||||||
| chr16:2443489 | T | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG00642.hp2 HG01099.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-160T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443489 | |||||||
| chr16:2443497 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.778-152G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443497 | |||||||
| chr16:2443622 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.778-27C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 8/16 | chr16 | 2443622 | |||||||
| chr16:2443807 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA18984.hp1 | splice_region_variant&intron_variant | LOW | c.929+7C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2443807 | |||||||
| chr16:2443817 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.929+17G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2443817 | |||||||
| chr16:2443834 | C | T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.929+34C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2443834 | |||||||
| chr16:2443835 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.929+35G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2443835 | |||||||
| chr16:2443838 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.929+38G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2443838 | |||||||
| chr16:2443848 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.929+48G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2443848 | |||||||
| chr16:2443894 | GA | G | 3 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 |
3 | HG02922.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.929+95delA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2443894 | |||||||
| chr16:2443924 | C | CT | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.929+137dupT | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 2443924 | ||||||
| chr16:2444019 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.929+219G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444019 | |||||||
| chr16:2444161 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.929+361C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444161 | |||||||
| chr16:2444163 | C | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(188): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.929+363C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444163 | |||||||
| chr16:2444180 | A | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0036 |
2 | HG02080.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.929+380A>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444180 | |||||||
| chr16:2444201 | G | C | 21 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(18): Show |
21 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.929+401G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444201 | |||||||
| chr16:2444208 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.929+408C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444208 | |||||||
| chr16:2444474 | G | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(189): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.929+674G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444474 | |||||||
| chr16:2444493 | G | C | 1 | a0001c0001t0004g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.929+693G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444493 | |||||||
| chr16:2444504 | A | G | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.929+704A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444504 | |||||||
| chr16:2444552 | C | T | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.929+752C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444552 | |||||||
| chr16:2444602 | C | CT | 5 | a0001c0001t0002g0246 a0001c0001t0004g0243 a0001c0001t0004g0244 others(2): Show |
5 | HG02559.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.929+814dupT | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 2444602 | ||||||
| chr16:2444773 | T | C | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.930-685T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444773 | |||||||
| chr16:2444900 | CT | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.930-544delT | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr16 | 2444900 | ||||||
| chr16:2444983 | C | CCT | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.930-475_930-474ins others(2): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2444983 | |||||||
| chr16:2445130 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.930-328C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2445130 | |||||||
| chr16:2445262 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.930-196C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2445262 | |||||||
| chr16:2445288 | G | A | 5 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0090 others(2): Show |
5 | HG00099.hp1 HG01106.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.930-170G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2445288 | |||||||
| chr16:2445454 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0003g0235 |
2 | HG00735.hp2 HG01167.hp1 |
splice_region_variant&intron_variant | LOW | c.930-4G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 9/16 | chr16 | 2445454 | |||||||
| chr16:2445670 | C | T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1094+48C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2445670 | |||||||
| chr16:2445726 | G | GT | 3 | a0001c0001t0002g0256 a0001c0001t0002g0257 a0001c0001t0002g0258 |
3 | HG01346.hp2 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1094+106dupT | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 2445726 | ||||||
| chr16:2445726 | G | GTT | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(168): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1094+105_1094+106d others(4): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 2445726 | ||||||
| chr16:2445726 | G | GTTT | 33 | a0001c0001t0001g0060 a0001c0001t0001g0067 a0001c0001t0001g0068 others(30): Show |
33 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.1094+106_1094+107i others(5): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 2445726 | ||||||
| chr16:2445726 | G | GTTTT | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0200 others(1): Show |
4 | HG02486.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1094+106_1094+107i others(6): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 2445726 | ||||||
| chr16:2445729 | G | GT | 7 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0036 others(4): Show |
7 | HG00735.hp1 HG01099.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1094+120dupT | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 2445729 | ||||||
| chr16:2445729 | G | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1094+107G>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2445729 | |||||||
| chr16:2445804 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1094+182C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2445804 | |||||||
| chr16:2445928 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1094+306T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2445928 | |||||||
| chr16:2446075 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1094+453G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2446075 | |||||||
| chr16:2446143 | C | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1094+521C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2446143 | |||||||
| chr16:2446222 | AGGCACAG others(30): Show |
A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0242 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1094+605_1094+641d others(39): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 2446222 | ||||||
| chr16:2446424 | C | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1094+802C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2446424 | |||||||
| chr16:2446445 | G | A | 3 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 |
3 | HG02922.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1094+823G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2446445 | |||||||
| chr16:2446573 | C | T | 10 | a0001c0001t0002g0248 a0001c0001t0002g0250 a0001c0001t0002g0251 others(7): Show |
10 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1094+951C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2446573 | |||||||
| chr16:2446657 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0006g0040 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1094+1035C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2446657 | |||||||
| chr16:2446748 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1094+1126T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2446748 | |||||||
| chr16:2446805 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1094+1183A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2446805 | |||||||
| chr16:2446965 | A | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1094+1343A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2446965 | |||||||
| chr16:2447009 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1094+1387C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2447009 | |||||||
| chr16:2447116 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1094+1494C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2447116 | |||||||
| chr16:2447275 | CT | C | 21 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0029 others(18): Show |
21 | HG00099.hp2 HG01069.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.1095-1562delT | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr16 | 2447275 | ||||||
| chr16:2447293 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1095-1562T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2447293 | |||||||
| chr16:2447339 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1095-1516C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2447339 | |||||||
| chr16:2447364 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1095-1491C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2447364 | |||||||
| chr16:2447380 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1095-1475C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2447380 | |||||||
| chr16:2447408 | C | A | 2 | a0001c0001t0001g0228 a0001c0001t0003g0235 |
2 | HG00735.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1095-1447C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2447408 | |||||||
| chr16:2447559 | G | A | 1 | a0001c0001t0001g0001 | 4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1095-1296G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2447559 | |||||||
| chr16:2447569 | G | A | 4 | a0001c0001t0001g0170 a0001c0001t0001g0197 a0001c0001t0001g0203 others(1): Show |
4 | HG00099.hp2 HG00741.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1095-1286G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2447569 | |||||||
| chr16:2447682 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1095-1173C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2447682 | |||||||
| chr16:2447788 | C | G | 1 | a0001c0001t0001g0037 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1095-1067C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2447788 | |||||||
| chr16:2448129 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1095-726G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2448129 | |||||||
| chr16:2448203 | G | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1095-652G>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2448203 | |||||||
| chr16:2448253 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1095-602C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2448253 | |||||||
| chr16:2448331 | C | G | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1095-524C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2448331 | |||||||
| chr16:2448336 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1095-519T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2448336 | |||||||
| chr16:2448723 | C | T | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1095-132C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2448723 | |||||||
| chr16:2448827 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1095-28A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2448827 | |||||||
| chr16:2448848 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(187): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
splice_region_variant&intron_variant | LOW | c.1095-7G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 10/16 | chr16 | 2448848 | |||||||
| chr16:2449010 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1218+32T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 11/16 | chr16 | 2449010 | |||||||
| chr16:2449177 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1219-105C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 11/16 | chr16 | 2449177 | |||||||
| chr16:2449181 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1219-101G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 11/16 | chr16 | 2449181 | |||||||
| chr16:2449244 | C | T | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1219-38C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 11/16 | chr16 | 2449244 | |||||||
| chr16:2449572 | G | A | 1 | a0001c0001t0006g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1399+110G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 12/16 | chr16 | 2449572 | |||||||
| chr16:2449589 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1399+127C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 12/16 | chr16 | 2449589 | |||||||
| chr16:2449785 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1400-43G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 12/16 | chr16 | 2449785 | |||||||
| chr16:2449785 | G | GTCCCCTC others(2): Show |
205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(202): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1400-33_1400-25dup others(9): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 2449785 | ||||||
| chr16:2449785 | G | GTCCCCTC others(20): Show |
2 | a0001c0001t0005g0048 a0001c0001t0005g0150 |
2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1400-26_1400-25ins others(27): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr16 | 2449785 | ||||||
| chr16:2449809 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1400-19G>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 12/16 | chr16 | 2449809 | |||||||
| chr16:2450070 | G | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1487+155G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450070 | |||||||
| chr16:2450242 | G | A | 1 | a0001c0001t0004g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1487+327G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450242 | |||||||
| chr16:2450336 | T | TA | 8 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0022 others(5): Show |
9 | HG01978.hp1 HG02451.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.1487+446dupA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 2450336 | ||||||
| chr16:2450336 | T | TAA | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(165): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1487+445_1487+446d others(4): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 2450336 | ||||||
| chr16:2450336 | T | TAAA | 38 | a0001c0001t0001g0061 a0001c0001t0001g0069 a0001c0001t0001g0073 others(35): Show |
38 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1487+444_1487+446d others(5): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 2450336 | ||||||
| chr16:2450380 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1487+465A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450380 | |||||||
| chr16:2450397 | G | C | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1487+482G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450397 | |||||||
| chr16:2450446 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1487+531G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450446 | |||||||
| chr16:2450509 | CA | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1487+610delA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr16 | 2450509 | ||||||
| chr16:2450568 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1487+653C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450568 | |||||||
| chr16:2450603 | C | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(187): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1487+688C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450603 | |||||||
| chr16:2450645 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1487+730G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450645 | |||||||
| chr16:2450746 | A | G | 5 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0185 others(2): Show |
5 | HG02572.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1487+831A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450746 | |||||||
| chr16:2450824 | C | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1487+909C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450824 | |||||||
| chr16:2450843 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(204): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1487+928A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450843 | |||||||
| chr16:2450913 | C | T | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1487+998C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450913 | |||||||
| chr16:2450966 | C | G | 5 | a0001c0001t0002g0246 a0001c0001t0004g0243 a0001c0001t0004g0244 others(2): Show |
5 | HG02559.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1487+1051C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2450966 | |||||||
| chr16:2451019 | C | T | 20 | a0001c0001t0002g0246 a0001c0001t0002g0248 a0001c0001t0002g0249 others(17): Show |
20 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.1487+1104C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2451019 | |||||||
| chr16:2451024 | C | T | 5 | a0001c0001t0002g0246 a0001c0001t0004g0243 a0001c0001t0004g0244 others(2): Show |
5 | HG02559.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1487+1109C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2451024 | |||||||
| chr16:2451055 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1487+1140G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2451055 | |||||||
| chr16:2451246 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1487+1331G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2451246 | |||||||
| chr16:2451480 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1487+1565C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2451480 | |||||||
| chr16:2451608 | T | C | 7 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(4): Show |
7 | HG02630.hp1 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1488-1602T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2451608 | |||||||
| chr16:2451673 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0136 a0001c0001t0001g0151 others(8): Show |
12 | HG00735.hp2 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1488-1537C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2451673 | |||||||
| chr16:2451831 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1488-1379C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2451831 | |||||||
| chr16:2451917 | C | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0115 |
2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1488-1293C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2451917 | |||||||
| chr16:2452265 | C | T | 6 | a0001c0001t0001g0041 a0001c0001t0002g0246 a0001c0001t0004g0243 others(3): Show |
6 | HG02559.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1488-945C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2452265 | |||||||
| chr16:2452268 | A | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0041 a0001c0001t0002g0246 others(7): Show |
10 | HG00738.hp1 HG02559.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1488-942A>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2452268 | |||||||
| chr16:2452640 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(206): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1488-570T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2452640 | |||||||
| chr16:2452672 | A | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0014 |
2 | HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1488-538A>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2452672 | |||||||
| chr16:2452694 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1488-516G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2452694 | |||||||
| chr16:2452742 | C | T | 3 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 |
3 | HG02922.hp2 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1488-468C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2452742 | |||||||
| chr16:2452776 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1488-434T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2452776 | |||||||
| chr16:2452777 | A | G | 10 | a0001c0001t0002g0248 a0001c0001t0002g0250 a0001c0001t0002g0251 others(7): Show |
10 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1488-433A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2452777 | |||||||
| chr16:2452829 | C | T | 1 | a0001c0001t0004g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1488-381C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2452829 | |||||||
| chr16:2452835 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0242 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1488-375C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2452835 | |||||||
| chr16:2453017 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1488-193T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 13/16 | chr16 | 2453017 | |||||||
| chr16:2453340 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1587+31T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 14/16 | chr16 | 2453340 | |||||||
| chr16:2453360 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0006g0040 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1588-50G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 14/16 | chr16 | 2453360 | |||||||
| chr16:2453367 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1588-43A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 14/16 | chr16 | 2453367 | |||||||
| chr16:2453562 | C | A | 1 | a0001c0001t0002g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1715+25C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2453562 | |||||||
| chr16:2453585 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0006g0040 |
2 | HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1715+48G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2453585 | |||||||
| chr16:2453600 | C | G | 1 | a0001c0001t0001g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1715+63C>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2453600 | |||||||
| chr16:2453778 | CCTGT | C | 5 | a0001c0001t0002g0246 a0001c0001t0004g0243 a0001c0001t0004g0244 others(2): Show |
5 | HG02559.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1715+242_1715+245d others(6): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2453778 | |||||||
| chr16:2453783 | G | A | 5 | a0001c0001t0002g0246 a0001c0001t0004g0243 a0001c0001t0004g0244 others(2): Show |
5 | HG02559.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1715+246G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2453783 | |||||||
| chr16:2453784 | G | C | 5 | a0001c0001t0002g0246 a0001c0001t0004g0243 a0001c0001t0004g0244 others(2): Show |
5 | HG02559.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1715+247G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2453784 | |||||||
| chr16:2453849 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1715+312G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2453849 | |||||||
| chr16:2453850 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0115 |
2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1715+313C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2453850 | |||||||
| chr16:2453985 | T | C | 8 | a0001c0001t0001g0105 a0001c0001t0001g0170 a0001c0001t0001g0190 others(5): Show |
8 | HG00099.hp2 HG00280.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.1715+448T>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2453985 | |||||||
| chr16:2454093 | G | A | 1 | a0001c0001t0012g0058 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1715+556G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2454093 | |||||||
| chr16:2454298 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1715+761G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2454298 | |||||||
| chr16:2454558 | C | A | 2 | a0001c0001t0002g0257 a0001c0001t0002g0258 |
2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1716-837C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2454558 | |||||||
| chr16:2454669 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1716-726G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2454669 | |||||||
| chr16:2454734 | G | A | 1 | a0001c0006t0002g0131 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1716-661G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2454734 | |||||||
| chr16:2454781 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1716-614C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2454781 | |||||||
| chr16:2454789 | G | A | 1 | a0001c0001t0002g0260 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1716-606G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2454789 | |||||||
| chr16:2454824 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1716-571C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2454824 | |||||||
| chr16:2454826 | G | A | 30 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0078 others(27): Show |
31 | HG00639.hp2 HG00735.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1716-569G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2454826 | |||||||
| chr16:2454928 | C | T | 4 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716-467C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2454928 | |||||||
| chr16:2454937 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1716-458G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2454937 | |||||||
| chr16:2455039 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1716-356G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2455039 | |||||||
| chr16:2455057 | C | CA | 58 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0021 others(55): Show |
59 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1716-313dupA | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr16 | 2455057 | ||||||
| chr16:2455069 | A | C | 1 | a0001c0001t0001g0014 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1716-326A>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2455069 | |||||||
| chr16:2455156 | G | T | 4 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716-239G>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2455156 | |||||||
| chr16:2455261 | T | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0047 |
3 | NA18943.hp1 NA19070.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1716-134T>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2455261 | |||||||
| chr16:2455334 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0111 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1716-61G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2455334 | |||||||
| chr16:2455349 | C | T | 4 | a0001c0001t0004g0243 a0001c0001t0004g0244 a0001c0001t0004g0245 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716-46C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 15/16 | chr16 | 2455349 | |||||||
| chr16:2455621 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1885+57C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2455621 | |||||||
| chr16:2455649 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0087 |
2 | NA18959.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1885+85C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2455649 | |||||||
| chr16:2455650 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1885+86G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2455650 | |||||||
| chr16:2455708 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1885+144C>T | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2455708 | |||||||
| chr16:2455865 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1885+301C>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2455865 | |||||||
| chr16:2456022 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(207): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1885+458A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2456022 | |||||||
| chr16:2456124 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1886-421G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2456124 | |||||||
| chr16:2456129 | G | C | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1886-416G>C | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2456129 | |||||||
| chr16:2456192 | CTCACTGC others(10): Show |
C | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1886-341_1886-325d others(19): Show |
CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr16 | 2456192 | ||||||
| chr16:2456289 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1886-256G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2456289 | |||||||
| chr16:2456305 | G | A | 10 | a0001c0001t0002g0250 a0001c0001t0002g0251 a0001c0001t0002g0252 others(7): Show |
10 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1886-240G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2456305 | |||||||
| chr16:2456412 | A | G | 11 | a0001c0001t0002g0248 a0001c0001t0002g0250 a0001c0001t0002g0251 others(8): Show |
11 | HG01346.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1886-133A>G | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2456412 | |||||||
| chr16:2456435 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1886-110G>A | CCNF | ENSG00000162063.13 | transcript | ENST00000397066.9 | protein_coding | 16/16 | chr16 | 2456435 |