Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51692 |
| ensemblid | ENSG00000119203.14 |
| hgncid | 2326 |
| symbol | CPSF3 |
| name | cleavage and polyadenylation specific factor 3 |
| refseq_nuc | NM_016207.4 |
| refseq_prot | NP_057291.1 |
| ensembl_nuc | ENST00000238112.8 |
| ensembl_prot | ENSP00000238112.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 9423654 |
| end | 9473101 |
| strand | + |
| ver | v1.2 |
| region | chr2:9423654-9473101 |
| region5000 | chr2:9418654-9478101 |
| regionname0 | CPSF3_chr2_9423654_9473101 |
| regionname5000 | CPSF3_chr2_9418654_9478101 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 684 | 229 | 86 | 60 | 40 | 10 | 31 | 18 | CPSF3_chr2_9418654_9478101 | CPSF3 | MSAIP others(679): Show |
chr2 | 9418654 | 9478101 |
| a0002 | 0/0 | 684 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | MSAIP others(679): Show |
chr2 | 9418654 | 9478101 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2052 | 203 | 63 | 57 | 40 | 10 | 31 | CPSF3_chr2_9418654_9478101 | CPSF3 | ATGTC others(2047): Show |
chr2 | 9418654 | 9478101 | ||
| a0001c0002 | 0/0 | 2052 | 21 | 18 | 3 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | ATGTC others(2047): Show |
chr2 | 9418654 | 9478101 | ||
| a0001c0003 | 0/0 | 2052 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | ATGTC others(2047): Show |
chr2 | 9418654 | 9478101 | ||
| a0001c0004 | 0/0 | 2052 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | ATGTC others(2047): Show |
chr2 | 9418654 | 9478101 | ||
| a0001c0005 | 0/0 | 2052 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | ATGTC others(2047): Show |
chr2 | 9418654 | 9478101 | ||
| a0002c0006 | 0/0 | 2052 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | ATGTC others(2047): Show |
chr2 | 9418654 | 9478101 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2259 | 202 | 63 | 56 | 40 | 10 | 31 | CPSF3_chr2_9418654_9478101 | CPSF3 | GGAAG others(2254): Show |
chr2 | 9418654 | 9478101 |
| a0001c0001t0002 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | GGAAG others(2254): Show |
chr2 | 9418654 | 9478101 |
| a0001c0002t0001 | 0/0 | 2259 | 21 | 18 | 3 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | GGAAG others(2254): Show |
chr2 | 9418654 | 9478101 |
| a0001c0003t0001 | 0/0 | 2259 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | GGAAG others(2254): Show |
chr2 | 9418654 | 9478101 |
| a0001c0004t0001 | 0/0 | 2259 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | GGAAG others(2254): Show |
chr2 | 9418654 | 9478101 |
| a0001c0005t0001 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | GGAAG others(2254): Show |
chr2 | 9418654 | 9478101 |
| a0002c0006t0001 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | GGAAG others(2254): Show |
chr2 | 9418654 | 9478101 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0002 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0004t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0001c0005t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| a0002c0006t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | IBS | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0164 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0153 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02809 | hp2 | a0001 | c0005 | t0001 | g0178 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0148 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0165 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0212 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0211 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG04204 | hp2 | a0002 | c0006 | t0001 | g0030 | SAS | STU | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0159 | AFR | YRI | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | YRI | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | LWK | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ASW | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | GIH | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | GIH | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | MSL | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | USA | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | LWK | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | LWK | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0188 | REF | REF | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0081 | REF | REF | CPSF3_chr2_9418654_9478101 | CPSF3 | chr2 | 9418654 | 9478101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9471438 | G | A | 1 | a0002 | 1 | HG04204.hp2 | missense_variant&splice_region_variant | MODERATE | c.1952G>A | p.Arg651Gln | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 17/18 | 2072/2259 | 1952/2055 | 651/684 | chr2 | 9471438 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9443562 | G | A | 1 | a0001c0005 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1143G>A | p.Lys381Lys | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/18 | 1263/2259 | 1143/2055 | 381/684 | chr2 | 9443562 | |||
| chr2:9443563 | T | C | 1 | a0001c0003 | 2 | HG02647.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.1144T>C | p.Leu382Leu | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/18 | 1264/2259 | 1144/2055 | 382/684 | chr2 | 9443563 | |||
| chr2:9448209 | T | C | 1 | a0001c0002 | 21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
synonymous_variant | LOW | c.1254T>C | p.His418His | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/18 | 1374/2259 | 1254/2055 | 418/684 | chr2 | 9448209 | |||
| chr2:9455693 | G | A | 1 | a0001c0004 | 2 | HG03195.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.1539G>A | p.Gln513Gln | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 13/18 | 1659/2259 | 1539/2055 | 513/684 | chr2 | 9455693 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9423677 | G | T | 1 | a0001c0001t0002 | 1 | HG00741.hp1 | 5_prime_UTR_variant | MODIFIER | c.-97G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/18 | 97 | chr2 | 9423677 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:9423943 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.50+120C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9423943 | |||||||
| chr2:9424067 | G | GA | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(35): Show |
40 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.50+254dupA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 9424067 | ||||||
| chr2:9424405 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0179 a0001c0001t0001g0180 others(32): Show |
38 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.50+582C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9424405 | |||||||
| chr2:9424537 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.50+714T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9424537 | |||||||
| chr2:9424597 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.50+774T>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9424597 | |||||||
| chr2:9424694 | T | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0179 a0001c0001t0001g0180 others(28): Show |
34 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.50+871T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9424694 | |||||||
| chr2:9424702 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0172 a0001c0001t0001g0173 others(4): Show |
8 | HG02145.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.50+879A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9424702 | |||||||
| chr2:9424744 | C | G | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.50+921C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9424744 | |||||||
| chr2:9424773 | G | T | 1 | a0001c0002t0001g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.50+950G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9424773 | |||||||
| chr2:9424897 | A | G | 1 | a0001c0002t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.50+1074A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9424897 | |||||||
| chr2:9424961 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.50+1138G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9424961 | |||||||
| chr2:9424994 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
106 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.50+1171A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9424994 | |||||||
| chr2:9425005 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.50+1182C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9425005 | |||||||
| chr2:9425039 | G | A | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.50+1216G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9425039 | |||||||
| chr2:9425140 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.50+1317G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9425140 | |||||||
| chr2:9425360 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.50+1537T>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9425360 | |||||||
| chr2:9425407 | AGATGAAT others(9): Show |
A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
132 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.50+1604_50+1619del others(16): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 9425407 | ||||||
| chr2:9425449 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.50+1626G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9425449 | |||||||
| chr2:9425479 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.50+1656T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9425479 | |||||||
| chr2:9425492 | C | T | 4 | a0001c0002t0001g0161 a0001c0002t0001g0162 a0001c0002t0001g0163 others(1): Show |
4 | HG02615.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.50+1669C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9425492 | |||||||
| chr2:9425531 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
11 | HG01106.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.50+1708G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9425531 | |||||||
| chr2:9425724 | G | A | 3 | a0001c0001t0001g0168 a0001c0003t0001g0164 a0001c0003t0001g0165 |
3 | HG02647.hp2 HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.50+1901G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9425724 | |||||||
| chr2:9425746 | GTTTACAT others(16): Show |
G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.50+1944_50+1966del others(23): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 9425746 | ||||||
| chr2:9425877 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.50+2054G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9425877 | |||||||
| chr2:9425969 | G | A | 1 | a0001c0005t0001g0178 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50+2146G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9425969 | |||||||
| chr2:9426011 | C | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.50+2188C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9426011 | |||||||
| chr2:9426017 | T | C | 1 | a0001c0001t0001g0015 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.50+2194T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9426017 | |||||||
| chr2:9426023 | G | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(13): Show |
21 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.50+2200G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9426023 | |||||||
| chr2:9426151 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.50+2328G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9426151 | |||||||
| chr2:9426411 | T | C | 1 | a0001c0002t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.51-2354T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9426411 | |||||||
| chr2:9426663 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.51-2102C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9426663 | |||||||
| chr2:9426672 | C | G | 19 | a0001c0002t0001g0009 a0001c0002t0001g0148 a0001c0002t0001g0149 others(16): Show |
20 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.51-2093C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9426672 | |||||||
| chr2:9426736 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.51-2029T>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9426736 | |||||||
| chr2:9426749 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(35): Show |
40 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.51-2016C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9426749 | |||||||
| chr2:9426784 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.51-1981A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9426784 | |||||||
| chr2:9426875 | C | CAAAA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
125 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(122): Show |
intron_variant | MODIFIER | c.51-1879_51-1876dup others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 9426875 | ||||||
| chr2:9426890 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0179 others(30): Show |
36 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.51-1875G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9426890 | |||||||
| chr2:9427202 | G | A | 2 | a0001c0002t0001g0148 a0001c0002t0001g0149 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.51-1563G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9427202 | |||||||
| chr2:9427211 | T | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.51-1554T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9427211 | |||||||
| chr2:9427315 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(31): Show |
37 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.51-1450T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9427315 | |||||||
| chr2:9427883 | T | A | 1 | a0001c0001t0001g0017 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.51-882T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9427883 | |||||||
| chr2:9427952 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.51-813A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9427952 | |||||||
| chr2:9427985 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.51-780T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9427985 | |||||||
| chr2:9427986 | A | T | 19 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(16): Show |
20 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.51-779A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9427986 | |||||||
| chr2:9427996 | A | AT | 25 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(22): Show |
25 | HG00642.hp1 HG00741.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.51-751dupT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 9427996 | ||||||
| chr2:9427996 | A | T | 1 | a0001c0002t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.51-769A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9427996 | |||||||
| chr2:9427996 | AT | A | 6 | a0001c0001t0001g0144 a0001c0001t0001g0172 a0001c0002t0001g0148 others(3): Show |
6 | HG00639.hp2 HG02615.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.51-751delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 9427996 | ||||||
| chr2:9428060 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.51-705G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428060 | |||||||
| chr2:9428157 | T | TGGCTAAT others(163): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(7): Show |
14 | HG01070.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.51-596_51-595insTT others(168): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 9428157 | ||||||
| chr2:9428157 | T | TGGCTAAT others(163): Show |
5 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
6 | HG01496.hp2 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.51-596_51-595insTT others(168): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 9428157 | ||||||
| chr2:9428157 | T | TGGCTAAT others(164): Show |
5 | a0001c0001t0001g0139 a0001c0001t0001g0143 a0001c0001t0001g0145 others(2): Show |
5 | HG02886.hp2 HG02895.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.51-596_51-595insTT others(169): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 9428157 | ||||||
| chr2:9428198 | G | A | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.51-567G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428198 | |||||||
| chr2:9428200 | G | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(17): Show |
25 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.51-565G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428200 | |||||||
| chr2:9428207 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(17): Show |
25 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.51-558A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428207 | |||||||
| chr2:9428211 | TG | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(17): Show |
25 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.51-551delG | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 9428211 | ||||||
| chr2:9428222 | A | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(17): Show |
25 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.51-543A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428222 | |||||||
| chr2:9428229 | T | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(17): Show |
25 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.51-536T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428229 | |||||||
| chr2:9428230 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.51-535C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428230 | |||||||
| chr2:9428239 | T | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(17): Show |
25 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.51-526T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428239 | |||||||
| chr2:9428243 | T | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(17): Show |
25 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.51-522T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428243 | |||||||
| chr2:9428316 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(35): Show |
40 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.51-449G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428316 | |||||||
| chr2:9428675 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.51-90A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428675 | |||||||
| chr2:9428688 | T | A | 2 | a0001c0004t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.51-77T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 1/17 | chr2 | 9428688 | |||||||
| chr2:9428994 | A | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0179 others(28): Show |
34 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.114+166A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 2/17 | chr2 | 9428994 | |||||||
| chr2:9429072 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.114+244A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 2/17 | chr2 | 9429072 | |||||||
| chr2:9429244 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.114+416G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 2/17 | chr2 | 9429244 | |||||||
| chr2:9429347 | C | A | 2 | a0001c0004t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.114+519C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 2/17 | chr2 | 9429347 | |||||||
| chr2:9429349 | T | C | 2 | a0001c0004t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.114+521T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 2/17 | chr2 | 9429349 | |||||||
| chr2:9429350 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.114+522T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 2/17 | chr2 | 9429350 | |||||||
| chr2:9429451 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
86 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.115-472C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 2/17 | chr2 | 9429451 | |||||||
| chr2:9429663 | C | T | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.115-260C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 2/17 | chr2 | 9429663 | |||||||
| chr2:9429843 | A | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
132 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.115-80A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 2/17 | chr2 | 9429843 | |||||||
| chr2:9430423 | CAGGGAGA others(1): Show |
C | 4 | a0001c0002t0001g0161 a0001c0002t0001g0162 a0001c0002t0001g0163 others(1): Show |
4 | HG02615.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.213-327_213-320del others(8): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 9430423 | ||||||
| chr2:9430733 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.213-19C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 3/17 | chr2 | 9430733 | |||||||
| chr2:9430925 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
132 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.341+45C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9430925 | |||||||
| chr2:9431125 | C | T | 1 | a0001c0002t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.341+245C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431125 | |||||||
| chr2:9431286 | T | C | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.341+406T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431286 | |||||||
| chr2:9431290 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.341+410G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431290 | |||||||
| chr2:9431520 | A | AAT | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
100 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.341+644_341+645dup others(2): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 9431520 | ||||||
| chr2:9431526 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
132 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.341+646C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431526 | |||||||
| chr2:9431529 | A | AT | 10 | a0001c0001t0001g0001 a0001c0001t0001g0133 a0001c0001t0001g0134 others(7): Show |
14 | HG01070.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.341+659dupT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 9431529 | ||||||
| chr2:9431529 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0174 a0001c0001t0002g0063 |
2 | HG00741.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.341+671_341+682del others(12): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 9431529 | ||||||
| chr2:9431530 | T | TA | 4 | a0001c0001t0001g0008 a0001c0001t0001g0130 a0001c0001t0001g0136 others(1): Show |
5 | HG01496.hp2 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.341+650_341+651ins others(1): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431530 | |||||||
| chr2:9431531 | T | A | 27 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(24): Show |
29 | HG00639.hp1 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.341+651T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431531 | |||||||
| chr2:9431533 | T | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.341+653T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431533 | |||||||
| chr2:9431539 | TC | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.341+660delC | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431539 | |||||||
| chr2:9431540 | C | T | 6 | a0001c0001t0001g0131 a0001c0001t0001g0180 a0001c0001t0001g0200 others(3): Show |
6 | HG01175.hp1 HG02280.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+660C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431540 | |||||||
| chr2:9431541 | T | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0209 |
2 | HG01175.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.341+661T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431541 | |||||||
| chr2:9431541 | T | TC | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0002t0001g0160 |
3 | HG02523.hp1 HG02698.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.341+661_341+662ins others(1): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431541 | |||||||
| chr2:9431542 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.341+662T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431542 | |||||||
| chr2:9431543 | T | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.341+663T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431543 | |||||||
| chr2:9431546 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(27): Show |
33 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.341+666T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431546 | |||||||
| chr2:9431547 | T | C | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0209 |
3 | HG01175.hp1 HG02523.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.341+667T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431547 | |||||||
| chr2:9431548 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.341+668T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431548 | |||||||
| chr2:9431551 | TC | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(80): Show |
88 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.341+672delC | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431551 | |||||||
| chr2:9431552 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(35): Show |
44 | HG01070.hp2 HG01109.hp1 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.341+672C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431552 | |||||||
| chr2:9431771 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.342-740G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431771 | |||||||
| chr2:9431808 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.342-703C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431808 | |||||||
| chr2:9431810 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.342-701C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431810 | |||||||
| chr2:9431855 | G | T | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(37): Show |
42 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.342-656G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9431855 | |||||||
| chr2:9432344 | T | TA | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
132 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.342-157dupA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr2 | 9432344 | ||||||
| chr2:9432400 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.342-111T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 4/17 | chr2 | 9432400 | |||||||
| chr2:9432758 | TA | T | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.519+81delA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 9432758 | ||||||
| chr2:9432759 | A | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(35): Show |
40 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.519+71A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9432759 | |||||||
| chr2:9432799 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(35): Show |
40 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.519+111C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9432799 | |||||||
| chr2:9432961 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.519+273T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9432961 | |||||||
| chr2:9432984 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(33): Show |
39 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.519+296A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9432984 | |||||||
| chr2:9433019 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG02523.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.519+331C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9433019 | |||||||
| chr2:9433288 | T | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-583T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9433288 | |||||||
| chr2:9433452 | A | G | 5 | a0001c0002t0001g0148 a0001c0002t0001g0149 a0001c0002t0001g0151 others(2): Show |
5 | HG00639.hp2 HG02615.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-419A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9433452 | |||||||
| chr2:9433537 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(33): Show |
39 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.520-334A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9433537 | |||||||
| chr2:9433665 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.520-206A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9433665 | |||||||
| chr2:9433693 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.520-178G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9433693 | |||||||
| chr2:9433697 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.520-174C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9433697 | |||||||
| chr2:9433853 | G | C | 2 | a0001c0003t0001g0164 a0001c0003t0001g0165 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.520-18G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 5/17 | chr2 | 9433853 | |||||||
| chr2:9433969 | T | C | 4 | a0001c0002t0001g0159 a0001c0002t0001g0161 a0001c0002t0001g0162 others(1): Show |
4 | HG02615.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+9T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9433969 | |||||||
| chr2:9434124 | T | C | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.609+164T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9434124 | |||||||
| chr2:9434316 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 |
4 | HG01496.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.609+356C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9434316 | |||||||
| chr2:9434413 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.609+453T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9434413 | |||||||
| chr2:9434586 | C | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG01099.hp2 HG01123.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.609+626C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9434586 | |||||||
| chr2:9434934 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.609+974T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9434934 | |||||||
| chr2:9435017 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.609+1057A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9435017 | |||||||
| chr2:9435490 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.610-721C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9435490 | |||||||
| chr2:9435491 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.610-720G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9435491 | |||||||
| chr2:9435609 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.610-602G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9435609 | |||||||
| chr2:9435664 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(31): Show |
37 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.610-547G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9435664 | |||||||
| chr2:9435857 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0003t0001g0164 others(1): Show |
4 | HG01358.hp2 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-354G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9435857 | |||||||
| chr2:9435968 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.610-243G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9435968 | |||||||
| chr2:9436133 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.610-78A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 6/17 | chr2 | 9436133 | |||||||
| chr2:9436424 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
132 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.760+63T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9436424 | |||||||
| chr2:9436511 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.760+150C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9436511 | |||||||
| chr2:9436514 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.760+153C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9436514 | |||||||
| chr2:9436628 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.760+267C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9436628 | |||||||
| chr2:9436642 | G | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0179 others(28): Show |
34 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.760+281G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9436642 | |||||||
| chr2:9436699 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 |
4 | HG01496.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.760+338A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9436699 | |||||||
| chr2:9436720 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG01099.hp2 HG01123.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.760+359G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9436720 | |||||||
| chr2:9436774 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.760+415_760+416ins others(21): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9436774 | ||||||
| chr2:9436774 | A | AAAAAAAA others(12): Show |
1 | a0001c0004t0001g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.760+415_760+416ins others(19): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9436774 | ||||||
| chr2:9436774 | A | AAAAAAAA others(12): Show |
1 | a0001c0004t0001g0212 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.760+415_760+416ins others(19): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9436774 | ||||||
| chr2:9436774 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0183 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.760+415_760+416ins others(21): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9436774 | ||||||
| chr2:9436774 | A | AAAAAAAA others(14): Show |
28 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(25): Show |
31 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.760+415_760+416ins others(21): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9436774 | ||||||
| chr2:9436774 | A | AAAAAAAA others(17): Show |
4 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
4 | HG02135.hp2 NA19070.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.760+415_760+416ins others(24): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9436774 | ||||||
| chr2:9436774 | A | AAATAATA others(2): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG01433.hp2 HG03239.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.760+427_760+435dup others(9): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9436774 | ||||||
| chr2:9436774 | A | AAATAATA others(8): Show |
23 | a0001c0001t0001g0049 a0001c0001t0001g0166 a0001c0002t0001g0009 others(20): Show |
24 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.760+421_760+435dup others(15): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9436774 | ||||||
| chr2:9436774 | A | AAATAATA others(14): Show |
32 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0014 others(29): Show |
33 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.760+415_760+435dup others(21): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9436774 | ||||||
| chr2:9436774 | A | AAATAATA others(17): Show |
5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0032 others(2): Show |
5 | HG01074.hp2 HG01934.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.760+435_760+436ins others(24): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9436774 | ||||||
| chr2:9436774 | A | AAATAATA others(20): Show |
1 | a0001c0001t0001g0020 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.760+435_760+436ins others(27): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9436774 | ||||||
| chr2:9436774 | A | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0177 |
2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.760+413A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9436774 | |||||||
| chr2:9437044 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.760+683C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9437044 | |||||||
| chr2:9437124 | C | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(13): Show |
21 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.760+763C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9437124 | |||||||
| chr2:9437130 | GT | G | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.760+770delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9437130 | |||||||
| chr2:9437394 | A | ACT | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.760+1034_760+1035d others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9437394 | ||||||
| chr2:9437427 | A | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0115 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.760+1066A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9437427 | |||||||
| chr2:9437800 | A | T | 2 | a0001c0003t0001g0164 a0001c0003t0001g0165 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.760+1439A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9437800 | |||||||
| chr2:9437941 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.760+1580G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9437941 | |||||||
| chr2:9438084 | A | T | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.760+1723A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9438084 | |||||||
| chr2:9438093 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.760+1732G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9438093 | |||||||
| chr2:9438154 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.760+1793A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9438154 | |||||||
| chr2:9438334 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.760+1973G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9438334 | |||||||
| chr2:9438500 | CT | C | 24 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(21): Show |
25 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.761-1972delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9438500 | ||||||
| chr2:9438596 | A | G | 2 | a0001c0004t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.761-1895A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9438596 | |||||||
| chr2:9438809 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.761-1682G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9438809 | |||||||
| chr2:9439093 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.761-1398C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9439093 | |||||||
| chr2:9439340 | G | T | 1 | a0001c0001t0002g0063 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.761-1151G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9439340 | |||||||
| chr2:9439472 | C | CA | 5 | a0001c0001t0001g0133 a0001c0001t0001g0182 a0001c0001t0001g0196 others(2): Show |
5 | HG01099.hp2 HG01175.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.761-1003dupA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9439472 | ||||||
| chr2:9439472 | C | CAA | 70 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
75 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.761-1004_761-1003d others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9439472 | ||||||
| chr2:9439472 | C | CAAA | 7 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0031 others(4): Show |
7 | HG02647.hp2 HG02976.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.761-1005_761-1003d others(5): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9439472 | ||||||
| chr2:9439479 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.761-1012A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9439479 | |||||||
| chr2:9439548 | C | T | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.761-943C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9439548 | |||||||
| chr2:9439729 | C | T | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.761-762C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9439729 | |||||||
| chr2:9439752 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.761-739G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9439752 | |||||||
| chr2:9440016 | C | CT | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.761-466dupT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9440016 | ||||||
| chr2:9440016 | CT | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(7): Show |
14 | HG01070.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.761-466delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9440016 | ||||||
| chr2:9440194 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.761-297G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9440194 | |||||||
| chr2:9440337 | C | G | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(39): Show |
44 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.761-154C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9440337 | |||||||
| chr2:9440411 | G | GT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
132 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.761-78dupT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 9440411 | ||||||
| chr2:9440470 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.761-21T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 7/17 | chr2 | 9440470 | |||||||
| chr2:9440752 | C | A | 2 | a0001c0004t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.936+86C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 8/17 | chr2 | 9440752 | |||||||
| chr2:9440798 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.936+132T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 8/17 | chr2 | 9440798 | |||||||
| chr2:9440906 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.936+240C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 8/17 | chr2 | 9440906 | |||||||
| chr2:9440927 | T | C | 1 | a0001c0001t0001g0011 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.936+261T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 8/17 | chr2 | 9440927 | |||||||
| chr2:9441090 | A | G | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.936+424A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 8/17 | chr2 | 9441090 | |||||||
| chr2:9441342 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.937-476A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 8/17 | chr2 | 9441342 | |||||||
| chr2:9441432 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.937-386T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 8/17 | chr2 | 9441432 | |||||||
| chr2:9441531 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(17): Show |
22 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.937-287C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 8/17 | chr2 | 9441531 | |||||||
| chr2:9441537 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(33): Show |
39 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.937-281G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 8/17 | chr2 | 9441537 | |||||||
| chr2:9441612 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
86 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.937-206C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 8/17 | chr2 | 9441612 | |||||||
| chr2:9442022 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1095+46C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 9/17 | chr2 | 9442022 | |||||||
| chr2:9442248 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1095+272G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 9/17 | chr2 | 9442248 | |||||||
| chr2:9442713 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(31): Show |
37 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1095+737G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 9/17 | chr2 | 9442713 | |||||||
| chr2:9442744 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1095+768C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 9/17 | chr2 | 9442744 | |||||||
| chr2:9442844 | C | T | 1 | a0001c0002t0001g0158 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1096-671C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 9/17 | chr2 | 9442844 | |||||||
| chr2:9442853 | C | CA | 10 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0035 others(7): Show |
10 | HG00642.hp1 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1096-652dupA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr2 | 9442853 | ||||||
| chr2:9442855 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1096-660A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 9/17 | chr2 | 9442855 | |||||||
| chr2:9442864 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
106 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.1096-651G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 9/17 | chr2 | 9442864 | |||||||
| chr2:9442915 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(31): Show |
37 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1096-600C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 9/17 | chr2 | 9442915 | |||||||
| chr2:9443000 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1096-515A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 9/17 | chr2 | 9443000 | |||||||
| chr2:9443693 | A | AG | 31 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0179 others(28): Show |
34 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.1242+35dupG | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 9443693 | ||||||
| chr2:9443728 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1242+67C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9443728 | |||||||
| chr2:9443793 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1242+132A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9443793 | |||||||
| chr2:9443891 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1242+230A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9443891 | |||||||
| chr2:9444140 | T | TTA | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0166 |
3 | HG03516.hp2 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1242+497_1242+498d others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 9444140 | ||||||
| chr2:9444140 | T | TTATA | 2 | a0001c0001t0001g0012 a0001c0001t0001g0049 |
2 | HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1242+495_1242+498d others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 9444140 | ||||||
| chr2:9444140 | T | TTATATA | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(33): Show |
38 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1242+493_1242+498d others(8): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 9444140 | ||||||
| chr2:9444140 | TTA | T | 16 | a0001c0001t0001g0139 a0001c0002t0001g0009 a0001c0002t0001g0147 others(13): Show |
17 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1242+497_1242+498d others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 9444140 | ||||||
| chr2:9444155 | TATA | T | 3 | a0001c0002t0001g0149 a0001c0002t0001g0151 a0001c0002t0001g0169 |
3 | HG00639.hp2 HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1242+495_1242+497d others(5): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444155 | |||||||
| chr2:9444156 | A | T | 6 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0143 others(3): Show |
6 | HG01099.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1242+495A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444156 | |||||||
| chr2:9444157 | TA | T | 8 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(5): Show |
8 | HG02109.hp2 HG02145.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1242+497delA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444157 | |||||||
| chr2:9444158 | A | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0016 others(51): Show |
58 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1242+497A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444158 | |||||||
| chr2:9444159 | T | TATATATA | 2 | a0001c0001t0001g0031 a0001c0001t0001g0042 |
2 | HG03831.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1242+498_1242+499i others(9): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444159 | |||||||
| chr2:9444160 | T | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(22): Show |
25 | HG00642.hp1 HG01099.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.1242+499T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444160 | |||||||
| chr2:9444161 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1242+500T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444161 | |||||||
| chr2:9444162 | T | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG03098.hp2 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1242+501T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444162 | |||||||
| chr2:9444214 | C | T | 21 | a0001c0001t0001g0135 a0001c0002t0001g0009 a0001c0002t0001g0147 others(18): Show |
22 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1242+553C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444214 | |||||||
| chr2:9444222 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1242+561G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444222 | |||||||
| chr2:9444337 | G | A | 1 | a0002c0006t0001g0030 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1242+676G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444337 | |||||||
| chr2:9444372 | C | T | 1 | a0001c0002t0001g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1242+711C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444372 | |||||||
| chr2:9444394 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0171 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1242+733G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444394 | |||||||
| chr2:9444500 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1242+839G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444500 | |||||||
| chr2:9444649 | G | C | 3 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02886.hp2 HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1242+988G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444649 | |||||||
| chr2:9444659 | GGTTT | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
132 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.1242+1020_1242+102 others(8): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 9444659 | ||||||
| chr2:9444726 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1242+1065G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444726 | |||||||
| chr2:9444791 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1242+1130G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444791 | |||||||
| chr2:9444812 | C | T | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1242+1151C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444812 | |||||||
| chr2:9444882 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1242+1221T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444882 | |||||||
| chr2:9444913 | G | A | 2 | a0001c0004t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1242+1252G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9444913 | |||||||
| chr2:9445071 | C | G | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(35): Show |
40 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1242+1410C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9445071 | |||||||
| chr2:9445248 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1242+1587A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9445248 | |||||||
| chr2:9445280 | G | C | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1242+1619G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9445280 | |||||||
| chr2:9445307 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1242+1646C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9445307 | |||||||
| chr2:9445410 | C | T | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(35): Show |
40 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1242+1749C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9445410 | |||||||
| chr2:9445553 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1242+1892G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9445553 | |||||||
| chr2:9445576 | C | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(31): Show |
37 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1242+1915C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9445576 | |||||||
| chr2:9445701 | T | C | 3 | a0001c0001t0001g0168 a0001c0003t0001g0164 a0001c0003t0001g0165 |
3 | HG02647.hp2 HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1242+2040T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9445701 | |||||||
| chr2:9445723 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0179 others(29): Show |
35 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1242+2062C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9445723 | |||||||
| chr2:9445736 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1242+2075C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9445736 | |||||||
| chr2:9446105 | C | G | 1 | a0001c0002t0001g0157 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1243-2093C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9446105 | |||||||
| chr2:9446107 | A | T | 5 | a0001c0002t0001g0159 a0001c0002t0001g0161 a0001c0002t0001g0162 others(2): Show |
5 | HG02615.hp2 HG03130.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1243-2091A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9446107 | |||||||
| chr2:9446211 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1243-1987G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9446211 | |||||||
| chr2:9446215 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1243-1983T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9446215 | |||||||
| chr2:9446436 | A | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1243-1762A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9446436 | |||||||
| chr2:9446580 | C | CA | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): Show |
90 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.1243-1598dupA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 9446580 | ||||||
| chr2:9446580 | CA | C | 15 | a0001c0001t0001g0139 a0001c0002t0001g0009 a0001c0002t0001g0148 others(12): Show |
16 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1243-1598delA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 9446580 | ||||||
| chr2:9446600 | A | G | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1243-1598A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9446600 | |||||||
| chr2:9446683 | C | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
107 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.1243-1515C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9446683 | |||||||
| chr2:9446714 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1243-1484G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9446714 | |||||||
| chr2:9446747 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1243-1451A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9446747 | |||||||
| chr2:9446754 | C | CA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(17): Show |
25 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1243-1434dupA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 9446754 | ||||||
| chr2:9447051 | G | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(31): Show |
37 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1243-1147G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9447051 | |||||||
| chr2:9447305 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0179 others(28): Show |
34 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.1243-893C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9447305 | |||||||
| chr2:9447818 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1243-380C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9447818 | |||||||
| chr2:9447822 | A | C | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1243-376A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9447822 | |||||||
| chr2:9447873 | A | G | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1243-325A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9447873 | |||||||
| chr2:9447962 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(33): Show |
39 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.1243-236A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 10/17 | chr2 | 9447962 | |||||||
| chr2:9448408 | ACTT | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG01433.hp2 HG03239.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395+62_1395+64del others(3): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9448408 | ||||||
| chr2:9448422 | T | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(17): Show |
25 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1395+72T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9448422 | |||||||
| chr2:9448560 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1395+210T>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9448560 | |||||||
| chr2:9448560 | T | TTG | 19 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(16): Show |
20 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1395+225_1395+226d others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9448560 | ||||||
| chr2:9448560 | TTG | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0052 others(13): Show |
18 | HG00423.hp1 HG01106.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.1395+225_1395+226d others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9448560 | ||||||
| chr2:9448562 | G | T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0050 others(34): Show |
40 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.1395+212G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9448562 | |||||||
| chr2:9448643 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1395+293G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9448643 | |||||||
| chr2:9448661 | A | T | 3 | a0001c0001t0001g0168 a0001c0003t0001g0164 a0001c0003t0001g0165 |
3 | HG02647.hp2 HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1395+311A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9448661 | |||||||
| chr2:9448700 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1395+350G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9448700 | |||||||
| chr2:9448713 | C | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(17): Show |
25 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1395+363C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9448713 | |||||||
| chr2:9448833 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1395+483G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9448833 | |||||||
| chr2:9448899 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1395+549A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9448899 | |||||||
| chr2:9449344 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1395+994C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9449344 | |||||||
| chr2:9449376 | C | T | 6 | a0001c0001t0001g0064 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG02040.hp1 NA18747.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395+1026C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9449376 | |||||||
| chr2:9449387 | A | G | 21 | a0001c0001t0001g0210 a0001c0002t0001g0009 a0001c0002t0001g0147 others(18): Show |
22 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1395+1037A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9449387 | |||||||
| chr2:9449490 | C | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0067 a0001c0001t0001g0101 others(1): Show |
5 | HG01358.hp1 HG01943.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1395+1140C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9449490 | |||||||
| chr2:9449558 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1395+1208G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9449558 | |||||||
| chr2:9449620 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1395+1270T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9449620 | |||||||
| chr2:9449743 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1395+1393A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9449743 | |||||||
| chr2:9450146 | A | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
86 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.1395+1796A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9450146 | |||||||
| chr2:9450147 | A | AT | 6 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0099 others(3): Show |
6 | HG00423.hp1 HG00738.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395+1820dupT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9450147 | ||||||
| chr2:9450147 | AT | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0037 others(11): Show |
18 | HG01099.hp2 HG01109.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1395+1820delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9450147 | ||||||
| chr2:9450177 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0213 |
2 | HG01167.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1395+1827A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9450177 | |||||||
| chr2:9450308 | C | A | 1 | a0001c0002t0001g0148 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1395+1958C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9450308 | |||||||
| chr2:9450399 | C | T | 20 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0148 others(17): Show |
21 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1395+2049C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9450399 | |||||||
| chr2:9450445 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | NA19070.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1395+2095G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9450445 | |||||||
| chr2:9450558 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1395+2208C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9450558 | |||||||
| chr2:9450596 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1395+2246T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9450596 | |||||||
| chr2:9450672 | C | T | 16 | a0001c0002t0001g0009 a0001c0002t0001g0147 a0001c0002t0001g0150 others(13): Show |
17 | HG00738.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1396-2241C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9450672 | |||||||
| chr2:9450926 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
127 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.1396-1987A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9450926 | |||||||
| chr2:9451082 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1396-1831A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451082 | |||||||
| chr2:9451148 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0047 others(52): Show |
59 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1396-1765G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451148 | |||||||
| chr2:9451182 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1396-1731T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451182 | |||||||
| chr2:9451376 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1396-1537G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451376 | |||||||
| chr2:9451395 | C | T | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1396-1518C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451395 | |||||||
| chr2:9451538 | C | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0124 |
2 | HG00741.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1396-1375C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451538 | |||||||
| chr2:9451645 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1396-1268C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451645 | |||||||
| chr2:9451674 | G | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(16): Show |
24 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.1396-1239G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451674 | |||||||
| chr2:9451716 | C | CT | 54 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0021 others(51): Show |
59 | HG00099.hp2 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1396-1178dupT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9451716 | ||||||
| chr2:9451716 | C | CTT | 20 | a0001c0001t0001g0023 a0001c0001t0001g0096 a0001c0001t0001g0098 others(17): Show |
20 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1396-1179_1396-117 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9451716 | ||||||
| chr2:9451716 | CT | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(37): Show |
42 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1396-1178delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9451716 | ||||||
| chr2:9451778 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1396-1135G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451778 | |||||||
| chr2:9451790 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(115): Show |
129 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.1396-1123C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451790 | |||||||
| chr2:9451844 | G | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 |
4 | HG01496.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-1069G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451844 | |||||||
| chr2:9451872 | A | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 |
4 | HG01496.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1396-1041A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451872 | |||||||
| chr2:9451940 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1396-973T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451940 | |||||||
| chr2:9451944 | G | A | 5 | a0001c0001t0001g0168 a0001c0002t0001g0009 a0001c0002t0001g0160 others(2): Show |
6 | HG01884.hp1 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-969G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9451944 | |||||||
| chr2:9452012 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1396-901G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9452012 | |||||||
| chr2:9452186 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1396-727G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9452186 | |||||||
| chr2:9452190 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01934.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1396-723A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9452190 | |||||||
| chr2:9452325 | CA | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0106 others(11): Show |
15 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1396-570delA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9452325 | ||||||
| chr2:9452325 | CAA | C | 13 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(10): Show |
13 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1396-571_1396-570d others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9452325 | ||||||
| chr2:9452325 | CAAAAAAA | C | 5 | a0001c0001t0001g0168 a0001c0002t0001g0009 a0001c0002t0001g0160 others(2): Show |
6 | HG01884.hp1 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-576_1396-570d others(9): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9452325 | ||||||
| chr2:9452325 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1396-582_1396-570d others(15): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9452325 | ||||||
| chr2:9452416 | T | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(13): Show |
21 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.1396-497T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9452416 | |||||||
| chr2:9452459 | T | G | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1396-454T>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9452459 | |||||||
| chr2:9452600 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1396-313G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9452600 | |||||||
| chr2:9452645 | C | T | 13 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(10): Show |
13 | HG00738.hp1 HG01109.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1396-268C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9452645 | |||||||
| chr2:9452878 | A | G | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | HG02055.hp1 HG03516.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1396-35A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | chr2 | 9452878 | |||||||
| chr2:9452898 | A | AT | 8 | a0001c0001t0001g0023 a0001c0001t0001g0073 a0001c0001t0001g0074 others(5): Show |
8 | HG00639.hp2 HG01123.hp1 HG01361.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1396-5dupT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 9452898 | ||||||
| chr2:9453185 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1504+164C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9453185 | |||||||
| chr2:9453205 | T | G | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1504+184T>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9453205 | |||||||
| chr2:9453754 | G | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(33): Show |
38 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1504+733G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9453754 | |||||||
| chr2:9453839 | T | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
90 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.1504+818T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9453839 | |||||||
| chr2:9453943 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
104 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1504+922T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9453943 | |||||||
| chr2:9453957 | T | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
104 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1504+936T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9453957 | |||||||
| chr2:9454223 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1504+1202C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9454223 | |||||||
| chr2:9454229 | A | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(16): Show |
24 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.1504+1208A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9454229 | |||||||
| chr2:9454478 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1505-1181A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9454478 | |||||||
| chr2:9454539 | C | CT | 13 | a0001c0001t0001g0053 a0001c0001t0001g0070 a0001c0001t0001g0072 others(10): Show |
13 | HG00099.hp1 HG01071.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1505-1099dupT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 9454539 | ||||||
| chr2:9454539 | CT | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(97): Show |
110 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.1505-1099delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 9454539 | ||||||
| chr2:9454539 | CTT | C | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG01070.hp2 HG01175.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1505-1100_1505-109 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 9454539 | ||||||
| chr2:9454539 | CTTT | C | 5 | a0001c0001t0001g0168 a0001c0002t0001g0009 a0001c0002t0001g0160 others(2): Show |
6 | HG01884.hp1 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505-1101_1505-109 others(7): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 9454539 | ||||||
| chr2:9454631 | A | G | 1 | a0001c0002t0001g0155 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1505-1028A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9454631 | |||||||
| chr2:9454635 | C | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(33): Show |
38 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1505-1024C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9454635 | |||||||
| chr2:9454638 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1505-1021G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9454638 | |||||||
| chr2:9454655 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1505-1004C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9454655 | |||||||
| chr2:9454690 | G | A | 1 | a0001c0002t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1505-969G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9454690 | |||||||
| chr2:9454754 | C | G | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1505-905C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9454754 | |||||||
| chr2:9454823 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1505-836C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9454823 | |||||||
| chr2:9455016 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
104 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1505-643T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9455016 | |||||||
| chr2:9455135 | CT | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0050 others(38): Show |
45 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1505-507delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 9455135 | ||||||
| chr2:9455205 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1505-454C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9455205 | |||||||
| chr2:9455261 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1505-398G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9455261 | |||||||
| chr2:9455285 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1505-374G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9455285 | |||||||
| chr2:9455289 | C | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(15): Show |
23 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.1505-370C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9455289 | |||||||
| chr2:9455364 | G | C | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1505-295G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9455364 | |||||||
| chr2:9455386 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1505-273G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9455386 | |||||||
| chr2:9455397 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1505-262G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9455397 | |||||||
| chr2:9455425 | C | T | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1505-234C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9455425 | |||||||
| chr2:9455640 | C | A | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1505-19C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 12/17 | chr2 | 9455640 | |||||||
| chr2:9456001 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1603+244A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 13/17 | chr2 | 9456001 | |||||||
| chr2:9456205 | GC | G | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1603+450delC | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 9456205 | ||||||
| chr2:9456257 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(7): Show |
14 | HG01070.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1603+500G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 13/17 | chr2 | 9456257 | |||||||
| chr2:9456491 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1604-442C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 13/17 | chr2 | 9456491 | |||||||
| chr2:9456525 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1604-408A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 13/17 | chr2 | 9456525 | |||||||
| chr2:9456572 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1604-361C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 13/17 | chr2 | 9456572 | |||||||
| chr2:9456780 | G | A | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1604-153G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 13/17 | chr2 | 9456780 | |||||||
| chr2:9457042 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
5 | HG01433.hp2 HG03239.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1698+15T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9457042 | |||||||
| chr2:9457147 | A | ATG | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(68): Show |
75 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1698+163_1698+164d others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 9457147 | ||||||
| chr2:9457147 | A | ATGTG | 41 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(38): Show |
46 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1698+161_1698+164d others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 9457147 | ||||||
| chr2:9457147 | A | ATGTGTG | 9 | a0001c0001t0001g0072 a0001c0001t0001g0079 a0001c0001t0001g0080 others(6): Show |
9 | HG00099.hp1 HG00741.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1698+159_1698+164d others(8): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 9457147 | ||||||
| chr2:9457147 | A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0088 a0001c0001t0001g0143 a0001c0002t0001g0149 others(2): Show |
5 | HG02615.hp1 HG03195.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1698+157_1698+164d others(10): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 9457147 | ||||||
| chr2:9457147 | ATG | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(25): Show |
35 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.1698+163_1698+164d others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 9457147 | ||||||
| chr2:9457147 | ATGTG | A | 9 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
10 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1698+161_1698+164d others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 9457147 | ||||||
| chr2:9457147 | ATGTGTG | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0168 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1698+159_1698+164d others(8): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 9457147 | ||||||
| chr2:9457147 | ATGTGTGT others(3): Show |
A | 5 | a0001c0001t0001g0210 a0001c0002t0001g0159 a0001c0002t0001g0161 others(2): Show |
5 | HG02615.hp2 HG03130.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1698+155_1698+164d others(12): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 9457147 | ||||||
| chr2:9457147 | ATGTGTGT others(7): Show |
A | 9 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(6): Show |
9 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1698+151_1698+164d others(16): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr2 | 9457147 | ||||||
| chr2:9457330 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1698+303T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9457330 | |||||||
| chr2:9457582 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
104 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1698+555A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9457582 | |||||||
| chr2:9457587 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1698+560G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9457587 | |||||||
| chr2:9457605 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1698+578G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9457605 | |||||||
| chr2:9457778 | A | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1698+751A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9457778 | |||||||
| chr2:9457785 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1698+758C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9457785 | |||||||
| chr2:9458008 | G | A | 1 | a0001c0002t0001g0148 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1698+981G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9458008 | |||||||
| chr2:9458055 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0180 a0001c0001t0001g0181 others(2): Show |
5 | HG02257.hp2 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1698+1028C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9458055 | |||||||
| chr2:9458278 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0105 a0001c0001t0001g0111 |
3 | HG00558.hp2 HG02135.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1698+1251C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9458278 | |||||||
| chr2:9459010 | G | T | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1699-521G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9459010 | |||||||
| chr2:9459093 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
104 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1699-438T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9459093 | |||||||
| chr2:9459223 | A | T | 1 | a0001c0002t0001g0155 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1699-308A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9459223 | |||||||
| chr2:9459310 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1699-221T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9459310 | |||||||
| chr2:9459435 | A | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(16): Show |
24 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.1699-96A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 14/17 | chr2 | 9459435 | |||||||
| chr2:9459638 | C | CT | 58 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(55): Show |
61 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1786+48dupT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9459638 | ||||||
| chr2:9459638 | C | CTT | 18 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0128 others(15): Show |
18 | HG00738.hp1 HG01099.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.1786+47_1786+48dup others(2): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9459638 | ||||||
| chr2:9459638 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1786+36_1786+48dup others(13): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9459638 | ||||||
| chr2:9459638 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1786+35_1786+48dup others(14): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9459638 | ||||||
| chr2:9459638 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1786+33_1786+48dup others(16): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9459638 | ||||||
| chr2:9459638 | CT | C | 8 | a0001c0001t0001g0106 a0001c0001t0001g0109 a0001c0001t0001g0119 others(5): Show |
8 | HG02257.hp2 HG02280.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1786+48delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9459638 | ||||||
| chr2:9459638 | CTT | C | 5 | a0001c0001t0001g0168 a0001c0002t0001g0009 a0001c0002t0001g0160 others(2): Show |
6 | HG01884.hp1 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786+47_1786+48del others(2): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9459638 | ||||||
| chr2:9459638 | CTTTTT | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1786+44_1786+48del others(5): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9459638 | ||||||
| chr2:9459638 | CTTTTTTT others(3): Show |
C | 2 | a0001c0002t0001g0150 a0001c0002t0001g0156 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1786+39_1786+48del others(10): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9459638 | ||||||
| chr2:9459719 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
104 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1786+101A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9459719 | |||||||
| chr2:9459736 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
104 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1786+118A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9459736 | |||||||
| chr2:9459750 | A | G | 1 | a0001c0002t0001g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1786+132A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9459750 | |||||||
| chr2:9459895 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0025 others(6): Show |
9 | HG01074.hp2 HG01099.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1786+277G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9459895 | |||||||
| chr2:9460214 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1786+596G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9460214 | |||||||
| chr2:9460226 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1786+608G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9460226 | |||||||
| chr2:9460346 | G | A | 5 | a0001c0001t0001g0168 a0001c0002t0001g0009 a0001c0002t0001g0160 others(2): Show |
6 | HG01884.hp1 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1786+728G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9460346 | |||||||
| chr2:9460352 | A | C | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1786+734A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9460352 | |||||||
| chr2:9460493 | G | A | 2 | a0001c0002t0001g0150 a0001c0002t0001g0156 |
2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1786+875G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9460493 | |||||||
| chr2:9460843 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1786+1225A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9460843 | |||||||
| chr2:9460844 | T | C | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1786+1226T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9460844 | |||||||
| chr2:9461253 | G | T | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1786+1635G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9461253 | |||||||
| chr2:9461288 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(16): Show |
24 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.1786+1670C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9461288 | |||||||
| chr2:9461289 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1786+1671G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9461289 | |||||||
| chr2:9461310 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1786+1692C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9461310 | |||||||
| chr2:9461532 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1786+1914G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9461532 | |||||||
| chr2:9461652 | A | C | 3 | a0001c0001t0001g0050 a0001c0004t0001g0211 a0001c0004t0001g0212 |
3 | HG03139.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1786+2034A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9461652 | |||||||
| chr2:9461728 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1786+2110G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9461728 | |||||||
| chr2:9461743 | C | CT | 9 | a0001c0001t0001g0131 a0001c0001t0001g0142 a0001c0001t0001g0144 others(6): Show |
10 | HG01070.hp2 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1786+2149dupT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9461743 | ||||||
| chr2:9461743 | C | CTT | 14 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(11): Show |
19 | HG01109.hp1 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1786+2148_1786+214 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9461743 | ||||||
| chr2:9461743 | CT | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(36): Show |
42 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1786+2149delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9461743 | ||||||
| chr2:9461743 | CTT | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(35): Show |
40 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1786+2148_1786+214 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9461743 | ||||||
| chr2:9461767 | TA | T | 12 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(9): Show |
12 | HG00738.hp1 HG01109.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1786+2152delA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9461767 | ||||||
| chr2:9461906 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0204 |
2 | HG02135.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1786+2288C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9461906 | |||||||
| chr2:9461995 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1786+2377C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9461995 | |||||||
| chr2:9462050 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1786+2432G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9462050 | |||||||
| chr2:9462119 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0111 |
2 | HG00558.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1786+2501G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9462119 | |||||||
| chr2:9462166 | T | G | 1 | a0001c0001t0002g0063 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1786+2548T>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9462166 | |||||||
| chr2:9462178 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
90 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.1786+2560C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9462178 | |||||||
| chr2:9462537 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1786+2919C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9462537 | |||||||
| chr2:9462548 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1786+2930G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9462548 | |||||||
| chr2:9462618 | C | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0050 others(35): Show |
41 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1786+3000C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9462618 | |||||||
| chr2:9462618 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1786+3000C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9462618 | |||||||
| chr2:9462619 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1786+3001G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9462619 | |||||||
| chr2:9462685 | G | A | 2 | a0001c0004t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1786+3067G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9462685 | |||||||
| chr2:9462869 | G | A | 1 | a0001c0003t0001g0164 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1786+3251G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9462869 | |||||||
| chr2:9463115 | G | C | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1786+3497G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9463115 | |||||||
| chr2:9463535 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(114): Show |
128 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.1786+3917T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9463535 | |||||||
| chr2:9463656 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1786+4038G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9463656 | |||||||
| chr2:9463692 | C | A | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1787-4015C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9463692 | |||||||
| chr2:9463705 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1787-4002A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9463705 | |||||||
| chr2:9463719 | T | C | 4 | a0001c0002t0001g0009 a0001c0002t0001g0160 a0001c0003t0001g0164 others(1): Show |
5 | HG01884.hp1 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1787-3988T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9463719 | |||||||
| chr2:9463744 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1787-3963G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9463744 | |||||||
| chr2:9463815 | G | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
90 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.1787-3892G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9463815 | |||||||
| chr2:9464024 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1787-3683C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9464024 | |||||||
| chr2:9464069 | A | ATG | 13 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(10): Show |
13 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1787-3616_1787-361 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9464069 | ||||||
| chr2:9464355 | T | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1787-3352T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9464355 | |||||||
| chr2:9464357 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1787-3350T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9464357 | |||||||
| chr2:9464524 | T | C | 1 | a0001c0001t0001g0006 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1787-3183T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9464524 | |||||||
| chr2:9464647 | A | G | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1787-3060A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9464647 | |||||||
| chr2:9464685 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1787-3022G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9464685 | |||||||
| chr2:9465118 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(7): Show |
14 | HG01070.hp2 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1787-2589A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9465118 | |||||||
| chr2:9465403 | C | T | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1787-2304C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9465403 | |||||||
| chr2:9465431 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1787-2276G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9465431 | |||||||
| chr2:9465542 | T | TAC | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG02055.hp1 HG03516.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1787-2144_1787-214 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9465542 | ||||||
| chr2:9465542 | TAC | T | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1787-2144_1787-214 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9465542 | ||||||
| chr2:9465563 | ACG | A | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(36): Show |
41 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1787-2135_1787-213 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9465563 | ||||||
| chr2:9465565 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0047 others(41): Show |
48 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.1787-2142G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9465565 | |||||||
| chr2:9465567 | G | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0014 others(35): Show |
39 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.1787-2140G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9465567 | |||||||
| chr2:9465568 | C | T | 1 | a0001c0002t0001g0148 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1787-2139C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9465568 | |||||||
| chr2:9465569 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1787-2138G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9465569 | |||||||
| chr2:9465865 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1787-1842A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9465865 | |||||||
| chr2:9465882 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1787-1825G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9465882 | |||||||
| chr2:9466043 | C | T | 1 | a0001c0002t0001g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1787-1664C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466043 | |||||||
| chr2:9466180 | GCA | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
90 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.1787-1517_1787-151 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466180 | ||||||
| chr2:9466181 | C | T | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1787-1526C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466181 | |||||||
| chr2:9466196 | TCA | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(27): Show |
36 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.1787-1501_1787-150 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466196 | ||||||
| chr2:9466198 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1787-1509A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466198 | |||||||
| chr2:9466200 | ACACACAC others(3): Show |
A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0105 a0001c0001t0001g0111 |
3 | HG00558.hp2 HG02135.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1787-1497_1787-148 others(14): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466200 | ||||||
| chr2:9466212 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0172 a0001c0001t0001g0173 others(4): Show |
8 | HG02145.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1787-1495A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466212 | |||||||
| chr2:9466214 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0172 a0001c0001t0001g0173 others(4): Show |
8 | HG02145.hp2 HG02257.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1787-1493A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466214 | |||||||
| chr2:9466217 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1787-1490C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466217 | |||||||
| chr2:9466222 | G | GCA | 4 | a0001c0001t0001g0168 a0001c0002t0001g0009 a0001c0002t0001g0160 others(1): Show |
5 | HG01884.hp1 HG02486.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1787-1475_1787-147 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466222 | ||||||
| chr2:9466226 | ACACACAC others(41): Show |
A | 2 | a0001c0004t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1787-1467_1787-142 others(52): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466226 | ||||||
| chr2:9466235 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1787-1472T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466235 | |||||||
| chr2:9466242 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1787-1465A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466242 | |||||||
| chr2:9466248 | GCGCACAC others(17): Show |
G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0050 others(33): Show |
40 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.1787-1448_1787-142 others(28): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466248 | ||||||
| chr2:9466249 | CGCACACA others(11): Show |
C | 1 | a0001c0002t0001g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1787-1457_1787-144 others(22): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466249 | |||||||
| chr2:9466250 | G | A | 4 | a0001c0001t0001g0023 a0001c0002t0001g0148 a0001c0002t0001g0151 others(1): Show |
4 | HG00639.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1457G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466250 | |||||||
| chr2:9466254 | A | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(38): Show |
43 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1787-1453A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466254 | |||||||
| chr2:9466258 | G | A | 4 | a0001c0001t0001g0023 a0001c0002t0001g0148 a0001c0002t0001g0151 others(1): Show |
4 | HG00639.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1449G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466258 | |||||||
| chr2:9466260 | A | G | 4 | a0001c0001t0001g0023 a0001c0002t0001g0148 a0001c0002t0001g0151 others(1): Show |
4 | HG00639.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1447A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466260 | |||||||
| chr2:9466260 | ACACAAAG others(7): Show |
A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(38): Show |
43 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1787-1442_1787-142 others(18): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466260 | ||||||
| chr2:9466261 | C | T | 4 | a0001c0001t0001g0023 a0001c0002t0001g0148 a0001c0002t0001g0151 others(1): Show |
4 | HG00639.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1446C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466261 | |||||||
| chr2:9466262 | A | G | 4 | a0001c0001t0001g0023 a0001c0002t0001g0148 a0001c0002t0001g0151 others(1): Show |
4 | HG00639.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1445A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466262 | |||||||
| chr2:9466264 | A | G | 4 | a0001c0001t0001g0023 a0001c0002t0001g0148 a0001c0002t0001g0151 others(1): Show |
4 | HG00639.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1443A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466264 | |||||||
| chr2:9466265 | A | C | 4 | a0001c0001t0001g0023 a0001c0002t0001g0148 a0001c0002t0001g0151 others(1): Show |
4 | HG00639.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1442A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466265 | |||||||
| chr2:9466266 | A | G | 4 | a0001c0001t0001g0023 a0001c0002t0001g0148 a0001c0002t0001g0151 others(1): Show |
4 | HG00639.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1441A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466266 | |||||||
| chr2:9466267 | G | C | 4 | a0001c0001t0001g0023 a0001c0002t0001g0148 a0001c0002t0001g0151 others(1): Show |
4 | HG00639.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1440G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466267 | |||||||
| chr2:9466274 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0050 others(33): Show |
40 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.1787-1433G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466274 | |||||||
| chr2:9466274 | G | GCA | 18 | a0001c0001t0001g0023 a0001c0002t0001g0147 a0001c0002t0001g0148 others(15): Show |
18 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1787-1427_1787-142 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466274 | ||||||
| chr2:9466282 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0098 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1787-1425G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466282 | |||||||
| chr2:9466285 | C | T | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1787-1422C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466285 | |||||||
| chr2:9466288 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1787-1419A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466288 | |||||||
| chr2:9466299 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
104 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1787-1408T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466299 | |||||||
| chr2:9466310 | ACT | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0050 others(33): Show |
39 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1787-1396_1787-139 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466310 | |||||||
| chr2:9466313 | GAC | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(33): Show |
38 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1787-1393_1787-139 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466313 | |||||||
| chr2:9466322 | A | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(33): Show |
38 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1787-1385A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466322 | |||||||
| chr2:9466323 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1787-1384C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466323 | |||||||
| chr2:9466326 | AGACG | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(33): Show |
38 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1787-1380_1787-137 others(8): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466326 | |||||||
| chr2:9466335 | C | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(33): Show |
38 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1787-1372C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466335 | |||||||
| chr2:9466336 | A | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(33): Show |
38 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1787-1371A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466336 | |||||||
| chr2:9466336 | A | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0047 others(45): Show |
52 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1787-1371A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466336 | |||||||
| chr2:9466338 | A | ACACAGGC others(3): Show |
13 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(10): Show |
13 | HG00738.hp1 HG01109.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1787-1366_1787-136 others(14): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466338 | ||||||
| chr2:9466340 | A | ACG | 2 | a0001c0001t0001g0070 a0001c0001t0001g0104 |
2 | HG03927.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1787-1355_1787-135 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466340 | ||||||
| chr2:9466340 | ACG | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(13): Show |
21 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.1787-1355_1787-135 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466340 | ||||||
| chr2:9466340 | ACGCG | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(31): Show |
36 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1787-1357_1787-135 others(8): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466340 | ||||||
| chr2:9466342 | G | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0047 others(60): Show |
67 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.1787-1365G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466342 | |||||||
| chr2:9466344 | G | A | 1 | a0001c0002t0001g0155 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1787-1363G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466344 | |||||||
| chr2:9466344 | G | GACCACA | 48 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0047 others(45): Show |
52 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1787-1363_1787-136 others(10): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466344 | |||||||
| chr2:9466346 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0210 a0001c0002t0001g0148 others(3): Show |
6 | HG00639.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1787-1361G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466346 | |||||||
| chr2:9466352 | G | A | 5 | a0001c0001t0001g0078 a0001c0001t0001g0093 a0001c0001t0001g0116 others(2): Show |
5 | HG00423.hp2 HG02040.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.1787-1355G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466352 | |||||||
| chr2:9466352 | G | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02886.hp2 HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1787-1355G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466352 | |||||||
| chr2:9466352 | GCA | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0172 |
2 | HG02523.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1787-1345_1787-134 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466352 | ||||||
| chr2:9466354 | A | G | 15 | a0001c0001t0001g0053 a0001c0002t0001g0147 a0001c0002t0001g0150 others(12): Show |
15 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1787-1353A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466354 | |||||||
| chr2:9466354 | A | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(13): Show |
21 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.1787-1353A>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466354 | |||||||
| chr2:9466356 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1787-1351A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466356 | |||||||
| chr2:9466370 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1787-1337A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466370 | |||||||
| chr2:9466372 | C | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(16): Show |
24 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.1787-1335C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466372 | |||||||
| chr2:9466380 | TCGCACAC others(3): Show |
T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(31): Show |
36 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.1787-1317_1787-130 others(14): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466380 | ||||||
| chr2:9466386 | ACACGCGC others(9): Show |
A | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1787-1307_1787-129 others(20): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466386 | ||||||
| chr2:9466390 | G | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0044 |
2 | HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.1787-1317G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466390 | |||||||
| chr2:9466396 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1787-1311A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466396 | |||||||
| chr2:9466406 | G | A | 2 | a0001c0004t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1787-1301G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466406 | |||||||
| chr2:9466408 | GCA | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 |
4 | HG01496.hp2 HG02717.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1787-1293_1787-129 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466408 | ||||||
| chr2:9466408 | GCACACAC others(11): Show |
G | 2 | a0001c0004t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1787-1293_1787-127 others(22): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466408 | ||||||
| chr2:9466414 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1787-1293A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466414 | |||||||
| chr2:9466416 | GCACACGC others(3): Show |
G | 1 | a0001c0001t0001g0119 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1787-1275_1787-126 others(14): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466416 | ||||||
| chr2:9466418 | ACACGCGC others(9): Show |
A | 5 | a0001c0001t0001g0168 a0001c0002t0001g0009 a0001c0002t0001g0160 others(2): Show |
6 | HG01884.hp1 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1787-1285_1787-127 others(20): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466418 | ||||||
| chr2:9466422 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1787-1285G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466422 | |||||||
| chr2:9466427 | C | G | 1 | a0001c0001t0001g0103 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1787-1280C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466427 | |||||||
| chr2:9466434 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG01361.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1787-1273G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466434 | |||||||
| chr2:9466434 | GCA | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1787-1264_1787-126 others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466434 | ||||||
| chr2:9466436 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1787-1271A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9466436 | |||||||
| chr2:9466595 | C | CTAAA | 15 | a0001c0001t0001g0168 a0001c0002t0001g0147 a0001c0002t0001g0150 others(12): Show |
15 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1787-1094_1787-109 others(8): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr2 | 9466595 | ||||||
| chr2:9467199 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1787-508T>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9467199 | |||||||
| chr2:9467499 | T | A | 1 | a0001c0001t0001g0024 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1787-208T>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9467499 | |||||||
| chr2:9467620 | C | G | 1 | a0001c0002t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1787-87C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 15/17 | chr2 | 9467620 | |||||||
| chr2:9467851 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1856+75C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9467851 | |||||||
| chr2:9468305 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(2): Show |
5 | HG02055.hp1 HG03516.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1856+529C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9468305 | |||||||
| chr2:9468616 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
104 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.1856+840G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9468616 | |||||||
| chr2:9468619 | C | CT | 8 | a0001c0001t0001g0054 a0001c0001t0001g0080 a0001c0001t0001g0085 others(5): Show |
8 | HG01106.hp1 HG01257.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1856+868dupT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 9468619 | ||||||
| chr2:9468619 | CT | C | 16 | a0001c0001t0001g0079 a0001c0001t0001g0136 a0001c0001t0001g0144 others(13): Show |
16 | HG00738.hp1 HG01109.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.1856+868delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 9468619 | ||||||
| chr2:9468619 | CTT | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0130 others(13): Show |
21 | HG01070.hp2 HG01109.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.1856+867_1856+868d others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 9468619 | ||||||
| chr2:9468619 | CTTTT | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(10): Show |
15 | HG01255.hp2 HG01433.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1856+865_1856+868d others(6): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 9468619 | ||||||
| chr2:9468619 | CTTTTT | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0014 others(37): Show |
41 | HG00642.hp1 HG00642.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1856+864_1856+868d others(7): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 9468619 | ||||||
| chr2:9468619 | CTTTTTT | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0050 others(27): Show |
33 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1856+863_1856+868d others(8): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 9468619 | ||||||
| chr2:9468758 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1856+982G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9468758 | |||||||
| chr2:9468858 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1856+1082C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9468858 | |||||||
| chr2:9469003 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1856+1227A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9469003 | |||||||
| chr2:9469097 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1856+1321A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9469097 | |||||||
| chr2:9469336 | A | G | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1856+1560A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9469336 | |||||||
| chr2:9469389 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1856+1613C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9469389 | |||||||
| chr2:9469433 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1856+1657G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9469433 | |||||||
| chr2:9469490 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1856+1714G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9469490 | |||||||
| chr2:9469921 | A | G | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1857-1422A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9469921 | |||||||
| chr2:9470190 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1857-1153C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470190 | |||||||
| chr2:9470679 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1857-664G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470679 | |||||||
| chr2:9470692 | G | A | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1857-651G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470692 | |||||||
| chr2:9470825 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 |
3 | HG02055.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1857-518G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470825 | |||||||
| chr2:9470834 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1857-509A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470834 | |||||||
| chr2:9470894 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-449T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470894 | |||||||
| chr2:9470895 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-448C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470895 | |||||||
| chr2:9470898 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-445G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470898 | |||||||
| chr2:9470899 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-444G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470899 | |||||||
| chr2:9470900 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-443C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470900 | |||||||
| chr2:9470907 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-436G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470907 | |||||||
| chr2:9470911 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-432C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470911 | |||||||
| chr2:9470914 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-429G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470914 | |||||||
| chr2:9470930 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-413C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470930 | |||||||
| chr2:9470937 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-406G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470937 | |||||||
| chr2:9470938 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-405G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470938 | |||||||
| chr2:9470940 | ATGGTGAC others(5): Show |
A | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-402_1857-391d others(14): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470940 | |||||||
| chr2:9470963 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-380C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470963 | |||||||
| chr2:9470965 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-378A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470965 | |||||||
| chr2:9470989 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-354G>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9470989 | |||||||
| chr2:9471021 | C | T | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1857-322C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471021 | |||||||
| chr2:9471034 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-309T>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471034 | |||||||
| chr2:9471035 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-308G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471035 | |||||||
| chr2:9471038 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-305A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471038 | |||||||
| chr2:9471039 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-304C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471039 | |||||||
| chr2:9471070 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-273T>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471070 | |||||||
| chr2:9471074 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-269T>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471074 | |||||||
| chr2:9471075 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-268G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471075 | |||||||
| chr2:9471077 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-266G>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471077 | |||||||
| chr2:9471087 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-256A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471087 | |||||||
| chr2:9471089 | C | T | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1857-254C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471089 | |||||||
| chr2:9471094 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1857-249A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471094 | |||||||
| chr2:9471138 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1857-205C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471138 | |||||||
| chr2:9471179 | G | A | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1857-164G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471179 | |||||||
| chr2:9471193 | C | A | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1857-150C>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471193 | |||||||
| chr2:9471213 | C | CA | 16 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0002t0001g0147 others(13): Show |
16 | HG00738.hp1 HG01109.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1857-119dupA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr2 | 9471213 | ||||||
| chr2:9471241 | A | G | 5 | a0001c0002t0001g0159 a0001c0002t0001g0161 a0001c0002t0001g0162 others(2): Show |
5 | HG02615.hp2 HG03130.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857-102A>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 16/17 | chr2 | 9471241 | |||||||
| chr2:9471462 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0057 |
4 | HG01243.hp1 HG01346.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1953+23G>A | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 17/17 | chr2 | 9471462 | |||||||
| chr2:9471611 | C | T | 2 | a0001c0001t0001g0168 a0001c0002t0001g0147 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1953+172C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 17/17 | chr2 | 9471611 | |||||||
| chr2:9471647 | C | T | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1953+208C>T | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 17/17 | chr2 | 9471647 | |||||||
| chr2:9471877 | C | G | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1953+438C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 17/17 | chr2 | 9471877 | |||||||
| chr2:9472006 | C | CA | 45 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0047 others(42): Show |
48 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1953+584dupA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 9472006 | ||||||
| chr2:9472006 | C | CAA | 47 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(44): Show |
49 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.1953+583_1953+584d others(4): Show |
CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 9472006 | ||||||
| chr2:9472227 | C | G | 14 | a0001c0002t0001g0147 a0001c0002t0001g0150 a0001c0002t0001g0152 others(11): Show |
14 | HG00738.hp1 HG01109.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1954-689C>G | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 17/17 | chr2 | 9472227 | |||||||
| chr2:9472319 | CA | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
99 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.1954-580delA | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 9472319 | ||||||
| chr2:9472545 | AT | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0192 a0001c0001t0001g0207 |
3 | HG01515.hp1 HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1954-369delT | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 9472545 | ||||||
| chr2:9472772 | A | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(114): Show |
128 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.1954-144A>C | CPSF3 | ENSG00000119203.14 | transcript | ENST00000238112.8 | protein_coding | 17/17 | chr2 | 9472772 |