Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55653 |
|---|---|
| ensemblid | ENSG00000124243.19 |
| hgncid | 14367 |
| symbol | BCAS4 |
| name | breast carcinoma amplified sequence 4 |
| refseq_nuc | NM_198799.4 |
| refseq_prot | NP_942094.3 |
| ensembl_nuc | ENST00000371608.8 |
| ensembl_prot | ENSP00000360669.3 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 50795061 |
| end | 50877177 |
| strand | + |
| ver | v1.2 |
| region | chr20:50795061-50877177 |
| region5000 | chr20:50790061-50882177 |
| regionname0 | BCAS4_chr20_50795061_50877177 |
| regionname5000 | BCAS4_chr20_50790061_50882177 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 173 | 211 | 72 | 53 | 62 | 5 | 17 | 38 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0002 | 0/0 | 173 | 51 | 8 | 8 | 21 | 1 | 13 | 13 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0003 | 0/0 | 173 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0004 | 0/0 | 173 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0005 | 0/0 | 173 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0006 | 0/0 | 173 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 522 | 190 | 54 | 51 | 61 | 5 | 17 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| c0002 | 0/0 | 522 | 51 | 8 | 8 | 21 | 1 | 13 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| c0003 | 0/0 | 522 | 11 | 9 | 2 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| c0004 | 0/0 | 522 | 9 | 8 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| c0005 | 0/0 | 522 | 5 | 4 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| c0006 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| c0007 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| c0008 | 0/0 | 522 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| c0009 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 593 | 112 | 20 | 33 | 36 | 4 | 17 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| t0002 | 0/0 | 593 | 95 | 34 | 12 | 36 | 2 | 11 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| t0003 | 0/0 | 593 | 29 | 12 | 9 | 8 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| t0004 | 0/0 | 593 | 16 | 7 | 2 | 6 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| t0005 | 0/0 | 593 | 9 | 6 | 3 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| t0006 | 0/0 | 593 | 4 | 3 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| t0007 | 0/0 | 593 | 2 | 0 | 2 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| t0008 | 0/0 | 593 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| t0009 | 0/0 | 593 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| t0010 | 0/0 | 593 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 522 | 190 | 54 | 51 | 61 | 5 | 17 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0003 | 0/0 | 522 | 11 | 9 | 2 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0004 | 0/0 | 522 | 9 | 8 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0008 | 0/0 | 522 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0002c0002 | 0/0 | 522 | 51 | 8 | 8 | 21 | 1 | 13 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0003c0005 | 0/0 | 522 | 5 | 4 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0004c0006 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0005c0007 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0006c0009 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1114 | 72 | 7 | 27 | 22 | 3 | 11 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0001t0002 | 0/0 | 1114 | 75 | 27 | 10 | 31 | 2 | 5 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0001t0003 | 0/0 | 1114 | 18 | 7 | 7 | 4 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0001t0004 | 0/0 | 1114 | 11 | 5 | 2 | 4 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0001t0005 | 0/0 | 1114 | 8 | 5 | 3 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0001t0006 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0001t0007 | 0/0 | 1114 | 2 | 0 | 2 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0001t0008 | 0/0 | 1114 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0001t0009 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0001t0010 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0003t0001 | 0/0 | 1114 | 11 | 9 | 2 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0004t0001 | 0/0 | 1114 | 2 | 1 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0004t0002 | 0/0 | 1114 | 3 | 3 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0004t0003 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0004t0004 | 0/0 | 1114 | 2 | 2 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0004t0005 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0001c0008t0001 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0002c0002t0001 | 0/0 | 1114 | 24 | 2 | 4 | 11 | 1 | 6 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0002c0002t0002 | 0/0 | 1114 | 14 | 2 | 2 | 4 | 0 | 6 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0002c0002t0003 | 0/0 | 1114 | 10 | 4 | 2 | 4 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0002c0002t0004 | 0/0 | 1114 | 3 | 0 | 0 | 2 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0003c0005t0002 | 0/0 | 1114 | 2 | 2 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0003c0005t0006 | 0/0 | 1114 | 3 | 2 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0004c0006t0001 | 0/0 | 1114 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0005c0007t0002 | 0/0 | 1114 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| a0006c0009t0001 | 0/0 | 1114 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | copy fasta | chr20 | 50790061 | 50882177 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0007g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0007g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0001t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0003t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0004t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0004t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0004t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0004t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0004t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0004t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0004t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0004t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0001c0008t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0002c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0003c0005t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0003c0005t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0003c0005t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0003c0005t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0003c0005t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0004c0006t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0005c0007t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| a0006c0009t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0155 | EUR | GBR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0083 | EUR | GBR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | CHS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | CHS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | CHS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | CHS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00621 | hp1 | a0001 | c0004 | t0001 | g0011 | EAS | CHS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0221 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0265 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0262 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0207 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0115 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0081 | AMR | PUR | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0068 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0095 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01361 | hp2 | a0003 | c0005 | t0006 | g0085 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0070 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0218 | EUR | IBS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01891 | hp2 | a0001 | c0004 | t0002 | g0015 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0054 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0098 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02027 | hp2 | a0002 | c0002 | t0003 | g0050 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02055 | hp2 | a0003 | c0005 | t0002 | g0128 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02132 | hp2 | a0002 | c0002 | t0003 | g0066 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02145 | hp1 | a0001 | c0004 | t0002 | g0009 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02148 | hp1 | a0002 | c0002 | t0003 | g0058 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | CDX | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | CDX | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02257 | hp1 | a0001 | c0004 | t0002 | g0016 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02258 | hp2 | a0002 | c0002 | t0003 | g0035 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0005 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PEL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0206 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0049 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0133 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0208 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0108 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0003 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0020 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02717 | hp1 | a0002 | c0002 | t0003 | g0038 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0026 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0187 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02886 | hp1 | a0003 | c0005 | t0006 | g0082 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02895 | hp2 | a0001 | c0004 | t0003 | g0008 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ESN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ESN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02976 | hp1 | a0001 | c0004 | t0005 | g0014 | AFR | ESN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0130 | AFR | ESN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03041 | hp2 | a0003 | c0005 | t0002 | g0078 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03098 | hp1 | a0001 | c0004 | t0004 | g0007 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03098 | hp2 | a0003 | c0005 | t0006 | g0084 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03139 | hp2 | a0001 | c0008 | t0001 | g0006 | AFR | ESN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ESN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0094 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0077 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03239 | hp2 | a0002 | c0002 | t0004 | g0043 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03486 | hp1 | a0001 | c0004 | t0004 | g0013 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ESN | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0255 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | GWD | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03579 | hp1 | a0002 | c0002 | t0003 | g0036 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03704 | hp1 | a0001 | c0001 | t0008 | g0258 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0067 | SAS | BEB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0021 | SAS | BEB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0033 | SAS | BEB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | STU | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0042 | SAS | STU | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | YRI | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | YRI | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | YRI | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0250 | AFR | YRI | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18968 | hp2 | a0005 | c0007 | t0002 | g0150 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0061 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18973 | hp1 | a0006 | c0009 | t0001 | g0010 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18983 | hp1 | a0004 | c0006 | t0001 | g0171 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19009 | hp1 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | LWK | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0057 | AFR | LWK | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | LWK | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | LWK | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19066 | hp1 | a0002 | c0002 | t0003 | g0045 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19068 | hp2 | a0002 | c0002 | t0004 | g0260 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | YRI | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | YRI | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | ASW | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | ASW | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0064 | SAS | GIH | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | GIH | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0096 | AFR | ACB | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | MSL | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | USA | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0214 | AFR | USA | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | USA | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | USA | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | LWK | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | LWK | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0110 | REF | REF | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0156 | REF | REF | BCAS4_chr20_50790061_50882177 | BCAS4 | chr20 | 50790061 | 50882177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:50795161
|
G | T | 1 | a0002 | 51 | HG00099.hp2 HG00408.hp1 HG01123.hp1 others(48): Show |
missense_variant | MODERATE | c.78G>T | p.Glu26Asp | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/5 | 101/1114 | 78/522 | 26/173 | chr20 | 50795161 | ||
| chr20:50830349
|
G | A | 1 | a0004 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.233G>A | p.Arg78His | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/5 | 256/1114 | 233/522 | 78/173 | chr20 | 50830349 | ||
| chr20:50841889
|
T | A | 1 | a0003 | 5 | HG01361.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
missense_variant | MODERATE | c.388T>A | p.Ser130Thr | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/5 | 411/1114 | 388/522 | 130/173 | chr20 | 50841889 | ||
| chr20:50841890
|
C | A | 1 | a0003 | 5 | HG01361.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
missense_variant | MODERATE | c.389C>A | p.Ser130Tyr | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/5 | 412/1114 | 389/522 | 130/173 | chr20 | 50841890 | ||
| chr20:50876538
|
C | T | 1 | a0005 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.452C>T | p.Thr151Met | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 475/1114 | 452/522 | 151/173 | chr20 | 50876538 | ||
| chr20:50876598
|
G | A | 1 | a0006 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.512G>A | p.Arg171Gln | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 535/1114 | 512/522 | 171/173 | chr20 | 50876598 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:50795152
|
G | T | 3 | a0001c0004a0001c0008a0006c0009 | 11 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(8): Show |
synonymous_variant | LOW | c.69G>T | p.Leu23Leu | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/5 | 92/1114 | 69/522 | 23/173 | chr20 | 50795152 | ||
| chr20:50876539
|
G | A | 2 | a0001c0003a0001c0008 | 12 | HG01243.hp2 HG01358.hp1 HG02280.hp2 others(9): Show |
synonymous_variant | LOW | c.453G>A | p.Thr151Thr | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 476/1114 | 453/522 | 151/173 | chr20 | 50876539 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:50876634
|
G | A | 7 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(4): Show | 42 | HG00408.hp2 HG00642.hp1 HG01106.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*26G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 26 | chr20 | 50876634 | |||||
| chr20:50876658
|
A | G | 7 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(4): Show | 42 | HG00408.hp2 HG00642.hp1 HG01106.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*50A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 50 | chr20 | 50876658 | |||||
| chr20:50876717
|
A | T | 2 | a0001c0001t0006a0003c0005t0006 | 4 | HG01361.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*109A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 109 | chr20 | 50876717 | |||||
| chr20:50876904
|
T | C | 3 | a0001c0001t0004a0001c0004t0004a0002c0002t0004 | 16 | HG00423.hp2 HG00558.hp2 HG01167.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*296T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 296 | chr20 | 50876904 | |||||
| chr20:50876930
|
C | T | 1 | a0001c0001t0010 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 322 | chr20 | 50876930 | |||||
| chr20:50876937
|
G | A | 2 | a0001c0001t0005a0001c0004t0005 | 9 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*329G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 329 | chr20 | 50876937 | |||||
| chr20:50876981
|
G | A | 1 | a0001c0001t0007 | 2 | HG01071.hp1 HG01099.hp2 |
3_prime_UTR_variant | MODIFIER | c.*373G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 373 | chr20 | 50876981 | |||||
| chr20:50877049
|
C | T | 1 | a0001c0001t0009 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*441C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 441 | chr20 | 50877049 | |||||
| chr20:50877072
|
G | A | 8 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(5): Show | 99 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*464G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 464 | chr20 | 50877072 | |||||
| chr20:50877129
|
C | T | 1 | a0001c0001t0008 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 5/5 | 521 | chr20 | 50877129 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:50795325
|
G | C | 17 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0003g0002others(14): Show | 17 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.90+152G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50795325 | ||||||
| chr20:50795326
|
C | A | 2 | a0001c0001t0001g0001a0001c0001t0003g0002 | 2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.90+153C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50795326 | ||||||
| chr20:50795344
|
C | A | 1 | a0002c0002t0002g0018 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.90+171C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50795344 | ||||||
| chr20:50795379
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.90+206C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50795379 | ||||||
| chr20:50795441
|
C | G | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.90+268C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50795441 | ||||||
| chr20:50795552
|
G | GGGCAGCC others(4): Show |
72 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0002g0017others(69): Show | 72 | HG00408.hp1 HG00621.hp1 HG01123.hp1 others(69): Show |
intron_variant | MODIFIER | c.90+382_90+383insAG others(9): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50795552 | |||||
| chr20:50795558
|
C | T | 14 | a0001c0001t0002g0017a0001c0003t0001g0004a0001c0003t0001g0005others(11): Show | 14 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+385C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50795558 | ||||||
| chr20:50795568
|
C | T | 11 | a0001c0004t0001g0011a0001c0004t0001g0012a0001c0004t0002g0009others(8): Show | 11 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+395C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50795568 | ||||||
| chr20:50795790
|
C | A | 16 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0003g0002others(13): Show | 16 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.90+617C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50795790 | ||||||
| chr20:50796084
|
A | T | 1 | a0001c0001t0002g0269 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.90+911A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796084 | ||||||
| chr20:50796368
|
C | CA | 16 | a0001c0001t0001g0075a0001c0001t0002g0017a0001c0001t0002g0074others(13): Show | 16 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.90+1206dupA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796368 | |||||
| chr20:50796396
|
C | CAT | 8 | a0001c0001t0001g0267a0001c0003t0001g0004a0001c0003t0001g0005others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.90+1237_90+1238dup others(2): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796396 | |||||
| chr20:50796403
|
A | G | 1 | a0001c0001t0002g0268 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.90+1230A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796403 | ||||||
| chr20:50796452
|
C | CATAT | 3 | a0001c0001t0001g0022a0001c0001t0002g0086a0001c0001t0002g0097 | 3 | HG00639.hp2 HG03195.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.90+1312_90+1315dup others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796452 | |||||
| chr20:50796452
|
C | CATATAT | 5 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0091others(2): Show | 5 | HG01255.hp1 HG01361.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+1310_90+1315dup others(6): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796452 | |||||
| chr20:50796452
|
CAT | C | 44 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0001g0234others(41): Show | 44 | HG01106.hp2 HG01346.hp1 HG01358.hp2 others(41): Show |
intron_variant | MODIFIER | c.90+1314_90+1315del others(2): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796452 | |||||
| chr20:50796452
|
CATAT | C | 11 | a0001c0001t0001g0228a0001c0001t0001g0246a0001c0001t0002g0229others(8): Show | 11 | HG01070.hp1 HG01099.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+1312_90+1315del others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796452 | |||||
| chr20:50796452
|
CATATATA others(7): Show |
C | 1 | a0001c0001t0002g0071 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.90+1302_90+1315del others(14): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796452 | |||||
| chr20:50796452
|
CATATATA others(11): Show |
C | 1 | a0001c0001t0007g0262 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.90+1298_90+1315del others(18): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796452 | |||||
| chr20:50796465
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0266 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.90+1294_90+1316del others(23): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796465 | |||||
| chr20:50796470
|
TATATATA others(10): Show |
T | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0007g0265 | 3 | HG01071.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.90+1298_90+1314del others(17): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796470 | ||||||
| chr20:50796472
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0002g0072 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.90+1300_90+1312del others(13): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796472 | ||||||
| chr20:50796473
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0003g0002 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.90+1302_90+1322del others(21): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796473 | |||||
| chr20:50796475
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.90+1304_90+1317del others(14): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796475 | |||||
| chr20:50796475
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.90+1304_90+1320del others(17): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796475 | |||||
| chr20:50796477
|
ATATATAT others(8): Show |
A | 3 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242 | 3 | HG03579.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.90+1306_90+1320del others(15): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796477 | |||||
| chr20:50796478
|
T | C | 1 | a0001c0001t0002g0076 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.90+1305T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796478 | ||||||
| chr20:50796478
|
TATA | T | 14 | a0001c0001t0001g0249a0001c0001t0001g0251a0001c0001t0001g0252others(11): Show | 14 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+1306_90+1308del others(3): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796478 | ||||||
| chr20:50796478
|
TATATA | T | 3 | a0001c0001t0001g0245a0001c0001t0002g0244a0001c0001t0003g0243 | 3 | HG02083.hp2 NA18968.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.90+1306_90+1310del others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796478 | ||||||
| chr20:50796479
|
ATATATAT others(8): Show |
A | 1 | a0001c0004t0001g0011 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.90+1308_90+1322del others(15): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796479 | |||||
| chr20:50796479
|
ATATATAT others(9): Show |
A | 4 | a0001c0004t0002g0015a0001c0004t0002g0016a0001c0004t0004g0013others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+1308_90+1323del others(16): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796479 | |||||
| chr20:50796480
|
TA | T | 4 | a0001c0001t0001g0238a0001c0001t0003g0065a0001c0001t0003g0239others(1): Show | 4 | HG01981.hp2 HG02055.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+1308delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796480 | ||||||
| chr20:50796480
|
TATA | T | 5 | a0001c0001t0002g0232a0002c0002t0001g0055a0002c0002t0001g0056others(2): Show | 5 | HG01496.hp1 HG01943.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.90+1308_90+1310del others(3): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796480 | ||||||
| chr20:50796481
|
A | T | 4 | a0001c0001t0002g0261a0002c0002t0001g0067a0002c0002t0002g0070others(1): Show | 4 | HG01433.hp2 HG03831.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+1308A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796481 | ||||||
| chr20:50796481
|
ATATATAT others(6): Show |
A | 1 | a0006c0009t0001g0010 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.90+1310_90+1322del others(13): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796481 | |||||
| chr20:50796481
|
ATATATAT others(8): Show |
A | 1 | a0001c0004t0002g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.90+1310_90+1324del others(15): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796481 | |||||
| chr20:50796482
|
TA | T | 11 | a0001c0001t0002g0220a0001c0001t0003g0219a0001c0001t0003g0222others(8): Show | 11 | HG00408.hp1 HG00642.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.90+1310delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796482 | ||||||
| chr20:50796482
|
TATA | T | 5 | a0001c0001t0005g0206a0001c0001t0005g0207a0001c0003t0001g0208others(2): Show | 5 | HG01167.hp2 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.90+1310_90+1312del others(3): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796482 | ||||||
| chr20:50796483
|
A | T | 42 | a0001c0001t0001g0234a0001c0001t0001g0237a0001c0001t0001g0238others(39): Show | 42 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.90+1310A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796483 | ||||||
| chr20:50796483
|
ATATATTT others(8): Show |
A | 2 | a0001c0004t0003g0008a0001c0004t0004g0007 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.90+1312_90+1326del others(15): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796483 | |||||
| chr20:50796485
|
A | ATT | 5 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0009g0026others(2): Show | 5 | HG02818.hp1 HG03195.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.90+1313_90+1314ins others(2): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796485 | |||||
| chr20:50796485
|
A | ATTT | 4 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0004g0195others(1): Show | 4 | HG02132.hp1 NA18963.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+1313_90+1314ins others(3): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796485 | |||||
| chr20:50796485
|
A | ATTTTT | 3 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0002g0197 | 3 | HG00423.hp1 HG02071.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.90+1313_90+1314ins others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796485 | |||||
| chr20:50796485
|
A | T | 93 | a0001c0001t0001g0075a0001c0001t0001g0205a0001c0001t0001g0212others(90): Show | 93 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.90+1312A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796485 | ||||||
| chr20:50796485
|
ATATTTTT others(5): Show |
A | 1 | a0001c0004t0001g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.90+1314_90+1325del others(12): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796485 | |||||
| chr20:50796485
|
ATATTTTT others(7): Show |
A | 1 | a0001c0008t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.90+1314_90+1327del others(14): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796485 | |||||
| chr20:50796487
|
A | ATATAT | 7 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0104others(4): Show | 7 | HG00621.hp2 HG01346.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+1315_90+1316ins others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796487 | |||||
| chr20:50796487
|
A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.90+1315_90+1316ins others(12): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796487 | |||||
| chr20:50796487
|
A | ATATATAT others(7): Show |
1 | a0001c0003t0001g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.90+1315_90+1316ins others(14): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796487 | |||||
| chr20:50796487
|
A | ATATATAT others(7): Show |
1 | a0002c0002t0001g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.90+1315_90+1316ins others(14): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796487 | |||||
| chr20:50796487
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0093 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.90+1315_90+1316ins others(11): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796487 | |||||
| chr20:50796487
|
A | ATATATAT others(6): Show |
2 | a0001c0003t0001g0094a0001c0003t0001g0095 | 2 | HG01358.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.90+1315_90+1316ins others(13): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796487 | |||||
| chr20:50796487
|
A | ATATATTT others(2): Show |
5 | a0001c0001t0001g0107a0001c0001t0001g0267a0001c0001t0002g0105others(2): Show | 5 | HG02647.hp2 HG02738.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+1315_90+1316ins others(9): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796487 | |||||
| chr20:50796487
|
A | ATATTT | 18 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0113others(15): Show | 18 | HG00558.hp1 HG00738.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.90+1315_90+1316ins others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796487 | |||||
| chr20:50796487
|
A | ATTTTT | 8 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0179others(5): Show | 8 | HG00280.hp2 HG01496.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.90+1336_90+1340dup others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796487 | |||||
| chr20:50796487
|
A | T | 130 | a0001c0001t0001g0075a0001c0001t0001g0188a0001c0001t0001g0196others(127): Show | 130 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.90+1314A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796487 | ||||||
| chr20:50796488
|
T | TA | 4 | a0001c0001t0001g0109a0001c0001t0006g0077a0001c0003t0001g0096others(1): Show | 4 | HG02015.hp2 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+1315_90+1316ins others(1): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796488 | ||||||
| chr20:50796488
|
T | TATA | 3 | a0001c0003t0001g0004a0003c0005t0002g0078a0003c0005t0006g0085 | 3 | HG01361.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.90+1315_90+1316ins others(3): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796488 | ||||||
| chr20:50796488
|
T | TATATA | 3 | a0001c0001t0001g0087a0001c0001t0003g0073a0002c0002t0002g0021 | 3 | HG02273.hp2 HG02293.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.90+1315_90+1316ins others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796488 | ||||||
| chr20:50796488
|
T | TATATATA others(4): Show |
1 | a0002c0002t0002g0020 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.90+1315_90+1316ins others(11): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796488 | ||||||
| chr20:50796489
|
T | A | 3 | a0001c0001t0002g0086a0001c0003t0001g0108a0003c0005t0006g0084 | 3 | HG02647.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.90+1316T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796489 | ||||||
| chr20:50796490
|
T | A | 8 | a0001c0001t0006g0077a0001c0003t0001g0004a0001c0003t0001g0005others(5): Show | 8 | HG01361.hp2 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.90+1317T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796490 | ||||||
| chr20:50796491
|
T | A | 1 | a0003c0005t0006g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.90+1318T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796491 | ||||||
| chr20:50796492
|
T | A | 6 | a0001c0001t0006g0077a0001c0003t0001g0004a0001c0003t0001g0005others(3): Show | 6 | HG02055.hp2 HG02280.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+1319T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796492 | ||||||
| chr20:50796493
|
T | A | 1 | a0003c0005t0006g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.90+1320T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796493 | ||||||
| chr20:50796494
|
T | A | 4 | a0001c0001t0006g0077a0003c0005t0002g0078a0003c0005t0002g0128others(1): Show | 4 | HG02055.hp2 HG02886.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.90+1321T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796494 | ||||||
| chr20:50796496
|
T | A | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.90+1323T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796496 | ||||||
| chr20:50796513
|
T | G | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.90+1340T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796513 | ||||||
| chr20:50796635
|
C | T | 69 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(66): Show | 69 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.90+1462C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796635 | ||||||
| chr20:50796638
|
G | A | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.90+1465G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796638 | ||||||
| chr20:50796640
|
G | A | 1 | a0002c0002t0001g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.90+1467G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796640 | ||||||
| chr20:50796677
|
G | A | 49 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0003g0065others(46): Show | 49 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(46): Show |
intron_variant | MODIFIER | c.90+1504G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796677 | ||||||
| chr20:50796759
|
G | C | 69 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(66): Show | 69 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.90+1586G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796759 | ||||||
| chr20:50796765
|
A | G | 11 | a0001c0004t0001g0011a0001c0004t0001g0012a0001c0004t0002g0009others(8): Show | 11 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+1592A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796765 | ||||||
| chr20:50796837
|
A | AT | 69 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(66): Show | 69 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.90+1677dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50796837 | |||||
| chr20:50796955
|
C | T | 14 | a0001c0001t0002g0017a0001c0003t0001g0004a0001c0003t0001g0005others(11): Show | 14 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+1782C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796955 | ||||||
| chr20:50796978
|
G | T | 2 | a0001c0001t0001g0001a0001c0001t0003g0002 | 2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.90+1805G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50796978 | ||||||
| chr20:50797277
|
A | T | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.90+2104A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50797277 | ||||||
| chr20:50797638
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0003g0002 | 2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.90+2465T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50797638 | ||||||
| chr20:50797678
|
T | G | 2 | a0001c0001t0003g0065a0001c0001t0004g0040 | 2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.90+2505T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50797678 | ||||||
| chr20:50797769
|
G | A | 2 | a0002c0002t0002g0041a0002c0002t0002g0046 | 2 | HG00408.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.90+2596G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50797769 | ||||||
| chr20:50797775
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.90+2602C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50797775 | ||||||
| chr20:50797815
|
G | A | 17 | a0002c0002t0001g0019a0002c0002t0001g0024a0002c0002t0001g0025others(14): Show | 17 | HG00408.hp1 HG01123.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.90+2642G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50797815 | ||||||
| chr20:50797822
|
C | T | 14 | a0001c0001t0002g0017a0001c0003t0001g0004a0001c0003t0001g0005others(11): Show | 14 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+2649C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50797822 | ||||||
| chr20:50797911
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.90+2738C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50797911 | ||||||
| chr20:50797956
|
T | A | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.90+2783T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50797956 | ||||||
| chr20:50797959
|
G | C | 64 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0002g0071others(61): Show | 64 | HG00408.hp1 HG00621.hp1 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.90+2786G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50797959 | ||||||
| chr20:50798066
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.90+2893C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798066 | ||||||
| chr20:50798141
|
C | T | 1 | a0002c0002t0003g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.90+2968C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798141 | ||||||
| chr20:50798205
|
A | C | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.90+3032A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798205 | ||||||
| chr20:50798296
|
A | AAAAC | 7 | a0001c0001t0001g0205a0001c0001t0002g0076a0001c0001t0002g0183others(4): Show | 7 | HG00423.hp2 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.90+3139_90+3142dup others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50798296 | |||||
| chr20:50798320
|
A | C | 1 | a0001c0001t0002g0182 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.90+3147A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798320 | ||||||
| chr20:50798399
|
A | G | 48 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0003g0065others(45): Show | 48 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(45): Show |
intron_variant | MODIFIER | c.90+3226A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798399 | ||||||
| chr20:50798407
|
CTTACG | C | 14 | a0001c0001t0002g0017a0001c0003t0001g0004a0001c0003t0001g0005others(11): Show | 14 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3235_90+3239del others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798407 | ||||||
| chr20:50798409
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0003g0002 | 2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.90+3236T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798409 | ||||||
| chr20:50798523
|
A | C | 2 | a0002c0002t0001g0019a0002c0002t0001g0028 | 2 | NA18950.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.90+3350A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798523 | ||||||
| chr20:50798538
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0002g0071others(61): Show | 64 | HG00408.hp1 HG00621.hp1 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.90+3365C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798538 | ||||||
| chr20:50798684
|
C | G | 14 | a0001c0001t0002g0017a0001c0003t0001g0004a0001c0003t0001g0005others(11): Show | 14 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3511C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798684 | ||||||
| chr20:50798780
|
C | T | 14 | a0001c0001t0002g0017a0001c0003t0001g0004a0001c0003t0001g0005others(11): Show | 14 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3607C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798780 | ||||||
| chr20:50798891
|
A | G | 1 | a0001c0001t0009g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.90+3718A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798891 | ||||||
| chr20:50798916
|
T | C | 16 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0003g0002others(13): Show | 16 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.90+3743T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798916 | ||||||
| chr20:50798944
|
C | A | 14 | a0001c0001t0002g0017a0001c0003t0001g0004a0001c0003t0001g0005others(11): Show | 14 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+3771C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798944 | ||||||
| chr20:50798953
|
T | C | 5 | a0003c0005t0002g0078a0003c0005t0002g0128a0003c0005t0006g0082others(2): Show | 5 | HG01361.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+3780T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50798953 | ||||||
| chr20:50799038
|
G | A | 6 | a0001c0001t0006g0077a0003c0005t0002g0078a0003c0005t0002g0128others(3): Show | 6 | HG01361.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+3865G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799038 | ||||||
| chr20:50799042
|
A | C | 3 | a0001c0001t0002g0127a0001c0001t0002g0169a0001c0001t0002g0170 | 3 | NA18950.hp1 NA18975.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.90+3869A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799042 | ||||||
| chr20:50799082
|
C | T | 11 | a0001c0004t0001g0011a0001c0004t0001g0012a0001c0004t0002g0009others(8): Show | 11 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+3909C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799082 | ||||||
| chr20:50799084
|
A | G | 1 | a0001c0001t0003g0203 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.90+3911A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799084 | ||||||
| chr20:50799285
|
G | A | 1 | a0002c0002t0003g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.90+4112G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799285 | ||||||
| chr20:50799358
|
C | T | 12 | a0001c0001t0002g0017a0001c0004t0001g0011a0001c0004t0001g0012others(9): Show | 12 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.90+4185C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799358 | ||||||
| chr20:50799506
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0002g0071others(61): Show | 64 | HG00408.hp1 HG00621.hp1 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.90+4333A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799506 | ||||||
| chr20:50799557
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.90+4384G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799557 | ||||||
| chr20:50799628
|
G | A | 1 | a0001c0001t0001g0110 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.90+4455G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799628 | ||||||
| chr20:50799664
|
C | T | 1 | a0001c0001t0004g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.90+4491C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799664 | ||||||
| chr20:50799666
|
T | C | 1 | a0001c0004t0001g0011 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.90+4493T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799666 | ||||||
| chr20:50799702
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.90+4529G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799702 | ||||||
| chr20:50799795
|
C | T | 6 | a0002c0002t0001g0042a0002c0002t0001g0048a0002c0002t0001g0059others(3): Show | 6 | HG01123.hp1 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+4622C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799795 | ||||||
| chr20:50799830
|
C | T | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.90+4657C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799830 | ||||||
| chr20:50799969
|
C | A | 2 | a0001c0001t0001g0001a0001c0001t0003g0002 | 2 | HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.90+4796C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50799969 | ||||||
| chr20:50800046
|
C | T | 11 | a0001c0004t0001g0011a0001c0004t0001g0012a0001c0004t0002g0009others(8): Show | 11 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+4873C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800046 | ||||||
| chr20:50800072
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.90+4899A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800072 | ||||||
| chr20:50800149
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0002g0071others(61): Show | 64 | HG00408.hp1 HG00621.hp1 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.90+4976T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800149 | ||||||
| chr20:50800256
|
G | T | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.90+5083G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800256 | ||||||
| chr20:50800520
|
A | G | 2 | a0002c0002t0001g0033a0002c0002t0001g0039 | 2 | HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.90+5347A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800520 | ||||||
| chr20:50800527
|
C | T | 1 | a0001c0003t0001g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.90+5354C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800527 | ||||||
| chr20:50800559
|
C | CT | 73 | a0001c0001t0001g0075a0001c0001t0001g0104a0001c0001t0001g0107others(70): Show | 73 | HG00280.hp2 HG00609.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.90+5407dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50800559 | |||||
| chr20:50800559
|
CT | C | 7 | a0001c0001t0001g0131a0001c0001t0002g0017a0001c0001t0002g0184others(4): Show | 7 | HG02976.hp2 HG03041.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.90+5407delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50800559 | |||||
| chr20:50800559
|
CTT | C | 41 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(38): Show | 41 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.90+5406_90+5407del others(2): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50800559 | |||||
| chr20:50800559
|
CTTT | C | 5 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0003g0065others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.90+5405_90+5407del others(3): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50800559 | |||||
| chr20:50800588
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0002g0071others(61): Show | 64 | HG00408.hp1 HG00621.hp1 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.90+5415C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800588 | ||||||
| chr20:50800623
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0164 | 2 | NA19074.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.90+5450G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800623 | ||||||
| chr20:50800723
|
G | A | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.90+5550G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800723 | ||||||
| chr20:50800781
|
C | G | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.90+5608C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800781 | ||||||
| chr20:50800813
|
C | T | 44 | a0001c0001t0003g0163a0002c0002t0001g0019a0002c0002t0001g0023others(41): Show | 44 | HG00408.hp1 HG00408.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.90+5640C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800813 | ||||||
| chr20:50800851
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.90+5678C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50800851 | ||||||
| chr20:50801142
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.90+5969G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801142 | ||||||
| chr20:50801148
|
C | T | 1 | a0002c0002t0001g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.90+5975C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801148 | ||||||
| chr20:50801208
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0002g0071others(61): Show | 64 | HG00408.hp1 HG00621.hp1 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.90+6035T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801208 | ||||||
| chr20:50801225
|
G | C | 1 | a0001c0004t0002g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.90+6052G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801225 | ||||||
| chr20:50801287
|
G | A | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.90+6114G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801287 | ||||||
| chr20:50801293
|
G | T | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.90+6120G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801293 | ||||||
| chr20:50801580
|
A | G | 6 | a0001c0001t0006g0077a0003c0005t0002g0078a0003c0005t0002g0128others(3): Show | 6 | HG01361.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+6407A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801580 | ||||||
| chr20:50801728
|
G | A | 1 | a0001c0003t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.90+6555G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801728 | ||||||
| chr20:50801862
|
A | G | 11 | a0001c0004t0001g0011a0001c0004t0001g0012a0001c0004t0002g0009others(8): Show | 11 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+6689A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801862 | ||||||
| chr20:50801864
|
C | A | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.90+6691C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801864 | ||||||
| chr20:50801893
|
A | T | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.90+6720A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801893 | ||||||
| chr20:50801904
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0002g0071a0001c0001t0002g0072others(6): Show | 9 | HG02280.hp2 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.90+6731C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801904 | ||||||
| chr20:50801990
|
G | A | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.90+6817G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801990 | ||||||
| chr20:50801995
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0002g0071a0001c0001t0002g0072others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+6822G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50801995 | ||||||
| chr20:50802228
|
C | T | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.90+7055C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50802228 | ||||||
| chr20:50802306
|
G | T | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.90+7133G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50802306 | ||||||
| chr20:50802327
|
C | T | 11 | a0001c0004t0001g0011a0001c0004t0001g0012a0001c0004t0002g0009others(8): Show | 11 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+7154C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50802327 | ||||||
| chr20:50802378
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.90+7205G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50802378 | ||||||
| chr20:50802496
|
T | C | 1 | a0001c0001t0003g0002 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.90+7323T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50802496 | ||||||
| chr20:50803079
|
G | T | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.90+7906G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50803079 | ||||||
| chr20:50803136
|
G | A | 1 | a0001c0001t0003g0002 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.90+7963G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50803136 | ||||||
| chr20:50803233
|
G | A | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.90+8060G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50803233 | ||||||
| chr20:50803246
|
A | C | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.90+8073A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50803246 | ||||||
| chr20:50803249
|
G | A | 12 | a0001c0001t0002g0017a0001c0004t0001g0011a0001c0004t0001g0012others(9): Show | 12 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.90+8076G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50803249 | ||||||
| chr20:50803340
|
T | G | 1 | a0001c0003t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.90+8167T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50803340 | ||||||
| chr20:50803579
|
A | C | 44 | a0001c0001t0002g0270a0002c0002t0001g0019a0002c0002t0001g0023others(41): Show | 44 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(41): Show |
intron_variant | MODIFIER | c.90+8406A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50803579 | ||||||
| chr20:50803801
|
C | CA | 19 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0267others(16): Show | 19 | HG00741.hp2 HG01975.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.90+8647dupA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50803801 | |||||
| chr20:50803801
|
C | CAA | 12 | a0001c0004t0001g0011a0001c0004t0001g0012a0001c0004t0002g0009others(9): Show | 12 | HG00621.hp1 HG01891.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.90+8646_90+8647dup others(2): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50803801 | |||||
| chr20:50803801
|
CA | C | 16 | a0001c0001t0001g0091a0001c0001t0001g0109a0001c0001t0001g0125others(13): Show | 16 | HG00423.hp2 HG00639.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.90+8647delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50803801 | |||||
| chr20:50803819
|
A | G | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.90+8646A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50803819 | ||||||
| chr20:50803959
|
G | C | 11 | a0001c0004t0001g0011a0001c0004t0001g0012a0001c0004t0002g0009others(8): Show | 11 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+8786G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50803959 | ||||||
| chr20:50803997
|
T | A | 7 | a0001c0001t0001g0001a0001c0001t0002g0071a0001c0001t0002g0072others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+8824T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50803997 | ||||||
| chr20:50804132
|
G | A | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.90+8959G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50804132 | ||||||
| chr20:50804239
|
A | G | 11 | a0001c0004t0001g0011a0001c0004t0001g0012a0001c0004t0002g0009others(8): Show | 11 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+9066A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50804239 | ||||||
| chr20:50804510
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0002g0071a0001c0001t0002g0072others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+9337G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50804510 | ||||||
| chr20:50804633
|
G | A | 7 | a0001c0001t0002g0111a0001c0001t0002g0137a0001c0001t0002g0138others(4): Show | 7 | HG00558.hp2 HG01952.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+9460G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50804633 | ||||||
| chr20:50804651
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.90+9478A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50804651 | ||||||
| chr20:50804987
|
G | A | 71 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(68): Show | 71 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.90+9814G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50804987 | ||||||
| chr20:50805024
|
A | G | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.90+9851A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50805024 | ||||||
| chr20:50805155
|
G | A | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.90+9982G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50805155 | ||||||
| chr20:50805234
|
C | T | 3 | a0001c0001t0002g0270a0001c0004t0001g0011a0006c0009t0001g0010 | 3 | HG00621.hp1 HG06807.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.90+10061C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50805234 | ||||||
| chr20:50805284
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(139): Show | 142 | HG00408.hp1 HG00609.hp1 HG00621.hp1 others(139): Show |
intron_variant | MODIFIER | c.90+10111A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50805284 | ||||||
| chr20:50805515
|
C | T | 1 | a0002c0002t0001g0060 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.90+10342C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50805515 | ||||||
| chr20:50805520
|
G | T | 1 | a0002c0002t0004g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.90+10347G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50805520 | ||||||
| chr20:50805891
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0002g0071others(62): Show | 65 | HG00408.hp1 HG00621.hp1 HG01123.hp1 others(62): Show |
intron_variant | MODIFIER | c.90+10718T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50805891 | ||||||
| chr20:50805896
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0002g0071a0001c0001t0002g0072others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+10723G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50805896 | ||||||
| chr20:50805901
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0002g0071others(62): Show | 65 | HG00408.hp1 HG00621.hp1 HG01123.hp1 others(62): Show |
intron_variant | MODIFIER | c.90+10728T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50805901 | ||||||
| chr20:50805976
|
C | CAA | 42 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(39): Show | 42 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.90+10817_90+10818d others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50805976 | |||||
| chr20:50805976
|
CA | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0205a0001c0001t0002g0071others(7): Show | 10 | HG01884.hp2 HG01943.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.90+10818delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50805976 | |||||
| chr20:50806064
|
T | C | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.90+10891T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50806064 | ||||||
| chr20:50806113
|
T | TAAATGGA others(30): Show |
1 | a0001c0001t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.90+10942_90+10978d others(39): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50806113 | |||||
| chr20:50806305
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0002g0071a0001c0001t0002g0072others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+11132G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50806305 | ||||||
| chr20:50806620
|
G | C | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.90+11447G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50806620 | ||||||
| chr20:50806647
|
C | T | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.90+11474C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50806647 | ||||||
| chr20:50806704
|
A | T | 7 | a0001c0001t0001g0001a0001c0001t0002g0071a0001c0001t0002g0072others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.91-11507A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50806704 | ||||||
| chr20:50806728
|
AGTAGGTA others(15): Show |
A | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.91-11482_91-11461d others(24): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50806728 | ||||||
| chr20:50806751
|
T | A | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.91-11460T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50806751 | ||||||
| chr20:50806772
|
G | A | 1 | a0001c0004t0002g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.91-11439G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50806772 | ||||||
| chr20:50806862
|
C | CT | 21 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0160others(18): Show | 21 | HG00408.hp2 HG01106.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.91-11322dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50806862 | |||||
| chr20:50806862
|
CT | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0173a0001c0001t0001g0175others(71): Show | 74 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.91-11322delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50806862 | |||||
| chr20:50806862
|
CTT | C | 10 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0003g0002others(7): Show | 10 | HG02257.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.91-11323_91-11322d others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50806862 | |||||
| chr20:50806862
|
CTTT | C | 12 | a0001c0001t0002g0017a0001c0001t0002g0270a0001c0004t0001g0011others(9): Show | 12 | HG00621.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.91-11324_91-11322d others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50806862 | |||||
| chr20:50806862
|
CTTTT | C | 41 | a0001c0004t0003g0008a0002c0002t0001g0019a0002c0002t0001g0023others(38): Show | 41 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.91-11325_91-11322d others(6): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50806862 | |||||
| chr20:50807098
|
C | T | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.91-11113C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50807098 | ||||||
| chr20:50807152
|
G | A | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.91-11059G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50807152 | ||||||
| chr20:50807193
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.91-11018G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50807193 | ||||||
| chr20:50807279
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.91-10932C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50807279 | ||||||
| chr20:50807308
|
C | T | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.91-10903C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50807308 | ||||||
| chr20:50807433
|
A | T | 1 | a0002c0002t0001g0023 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.91-10778A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50807433 | ||||||
| chr20:50807625
|
A | C | 18 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0002g0174others(15): Show | 18 | HG01106.hp2 HG01167.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.91-10586A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50807625 | ||||||
| chr20:50807902
|
C | CT | 47 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0002g0138others(44): Show | 47 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(44): Show |
intron_variant | MODIFIER | c.91-10290dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50807902 | |||||
| chr20:50807902
|
CT | C | 8 | a0001c0001t0002g0137a0001c0003t0001g0004a0001c0003t0001g0005others(5): Show | 8 | HG01891.hp2 HG02135.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.91-10290delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50807902 | |||||
| chr20:50807905
|
T | G | 6 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0003g0223others(3): Show | 6 | HG01167.hp2 HG01261.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-10306T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50807905 | ||||||
| chr20:50808027
|
C | T | 87 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(84): Show | 87 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.91-10184C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50808027 | ||||||
| chr20:50808057
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0140 | 2 | HG01074.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.91-10154G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50808057 | ||||||
| chr20:50808101
|
A | G | 1 | a0002c0002t0003g0053 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.91-10110A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50808101 | ||||||
| chr20:50808114
|
A | G | 69 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(66): Show | 69 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.91-10097A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50808114 | ||||||
| chr20:50808125
|
G | A | 1 | a0002c0002t0003g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.91-10086G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50808125 | ||||||
| chr20:50808196
|
G | A | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.91-10015G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50808196 | ||||||
| chr20:50808211
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(134): Show | 137 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.91-10000T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50808211 | ||||||
| chr20:50808263
|
C | G | 1 | a0002c0002t0002g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.91-9948C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50808263 | ||||||
| chr20:50808519
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(134): Show | 137 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.91-9692G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50808519 | ||||||
| chr20:50808848
|
C | T | 1 | a0001c0004t0002g0016 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.91-9363C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50808848 | ||||||
| chr20:50808965
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.91-9246G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50808965 | ||||||
| chr20:50809023
|
G | A | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0176others(2): Show | 5 | HG00099.hp2 HG01070.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-9188G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809023 | ||||||
| chr20:50809153
|
G | T | 1 | a0001c0001t0001g0245 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91-9058G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809153 | ||||||
| chr20:50809206
|
AT | A | 79 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(76): Show | 79 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.91-8993delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50809206 | |||||
| chr20:50809218
|
T | A | 6 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0003g0002others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-8993T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809218 | ||||||
| chr20:50809255
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0164 | 2 | NA19074.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.91-8956G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809255 | ||||||
| chr20:50809271
|
G | A | 44 | a0001c0001t0001g0075a0002c0002t0001g0019a0002c0002t0001g0023others(41): Show | 44 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(41): Show |
intron_variant | MODIFIER | c.91-8940G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809271 | ||||||
| chr20:50809460
|
C | T | 46 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0002g0270others(43): Show | 46 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.91-8751C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809460 | ||||||
| chr20:50809550
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0126 | 2 | NA18964.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.91-8661A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809550 | ||||||
| chr20:50809564
|
C | T | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.91-8647C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809564 | ||||||
| chr20:50809568
|
G | A | 43 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(40): Show | 43 | HG00408.hp1 HG01123.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.91-8643G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809568 | ||||||
| chr20:50809747
|
T | C | 15 | a0001c0001t0001g0198a0001c0001t0006g0077a0001c0003t0001g0004others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.91-8464T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809747 | ||||||
| chr20:50809779
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.91-8432T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809779 | ||||||
| chr20:50809826
|
G | C | 1 | a0001c0001t0001g0259 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.91-8385G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809826 | ||||||
| chr20:50809924
|
C | T | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.91-8287C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50809924 | ||||||
| chr20:50810182
|
A | G | 3 | a0002c0002t0001g0063a0002c0002t0002g0062a0002c0002t0002g0064 | 3 | HG03490.hp1 HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.91-8029A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810182 | ||||||
| chr20:50810331
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.91-7880C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810331 | ||||||
| chr20:50810400
|
G | A | 15 | a0001c0001t0001g0198a0001c0001t0006g0077a0001c0003t0001g0004others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.91-7811G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810400 | ||||||
| chr20:50810415
|
G | T | 6 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0003g0002others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-7796G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810415 | ||||||
| chr20:50810451
|
G | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(140): Show | 143 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.91-7760G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810451 | ||||||
| chr20:50810523
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.91-7688G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810523 | ||||||
| chr20:50810585
|
T | G | 1 | a0001c0001t0003g0002 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.91-7626T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810585 | ||||||
| chr20:50810589
|
G | GT | 56 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0120others(53): Show | 56 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.91-7606dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50810589 | |||||
| chr20:50810589
|
GT | G | 67 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(64): Show | 67 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.91-7606delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50810589 | |||||
| chr20:50810627
|
G | A | 6 | a0001c0001t0001g0087a0001c0001t0001g0114a0001c0001t0001g0125others(3): Show | 6 | HG01074.hp1 HG01975.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-7584G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810627 | ||||||
| chr20:50810715
|
C | T | 77 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(74): Show | 77 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.91-7496C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810715 | ||||||
| chr20:50810757
|
A | C | 15 | a0001c0001t0001g0198a0001c0001t0006g0077a0001c0003t0001g0004others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.91-7454A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810757 | ||||||
| chr20:50810886
|
G | A | 5 | a0003c0005t0002g0078a0003c0005t0002g0128a0003c0005t0006g0082others(2): Show | 5 | HG01361.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-7325G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810886 | ||||||
| chr20:50810891
|
T | C | 12 | a0001c0001t0001g0198a0001c0004t0001g0011a0001c0004t0001g0012others(9): Show | 12 | HG00423.hp1 HG00621.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-7320T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50810891 | ||||||
| chr20:50811076
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.91-7135C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50811076 | ||||||
| chr20:50811079
|
C | T | 1 | a0001c0004t0002g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.91-7132C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50811079 | ||||||
| chr20:50811167
|
A | C | 15 | a0001c0001t0001g0198a0001c0001t0006g0077a0001c0003t0001g0004others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.91-7044A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50811167 | ||||||
| chr20:50811405
|
T | C | 5 | a0001c0004t0001g0012a0001c0004t0002g0015a0001c0004t0002g0016others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-6806T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50811405 | ||||||
| chr20:50811875
|
A | G | 77 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(74): Show | 77 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.91-6336A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50811875 | ||||||
| chr20:50812024
|
T | C | 5 | a0003c0005t0002g0078a0003c0005t0002g0128a0003c0005t0006g0082others(2): Show | 5 | HG01361.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-6187T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812024 | ||||||
| chr20:50812102
|
A | G | 3 | a0001c0001t0006g0077a0001c0003t0001g0004a0001c0003t0001g0005 | 3 | HG02280.hp2 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.91-6109A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812102 | ||||||
| chr20:50812121
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.91-6090G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812121 | ||||||
| chr20:50812142
|
A | T | 84 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(81): Show | 84 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.91-6069A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812142 | ||||||
| chr20:50812155
|
T | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(137): Show | 140 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.91-6056T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812155 | ||||||
| chr20:50812294
|
G | A | 1 | a0001c0001t0003g0002 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.91-5917G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812294 | ||||||
| chr20:50812307
|
T | C | 1 | a0001c0001t0005g0207 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.91-5904T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812307 | ||||||
| chr20:50812308
|
AT | A | 4 | a0002c0002t0001g0048a0002c0002t0001g0059a0002c0002t0003g0054others(1): Show | 4 | HG01123.hp1 HG01346.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-5897delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50812308 | |||||
| chr20:50812323
|
C | T | 6 | a0001c0001t0002g0192a0001c0001t0002g0213a0001c0001t0002g0215others(3): Show | 6 | HG02922.hp2 HG03195.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.91-5888C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812323 | ||||||
| chr20:50812325
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.91-5886G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812325 | ||||||
| chr20:50812376
|
G | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0140 | 2 | HG01074.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.91-5835G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812376 | ||||||
| chr20:50812376
|
GC | G | 36 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0006g0077others(33): Show | 36 | HG01123.hp1 HG01346.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.91-5828delC | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50812376 | |||||
| chr20:50812382
|
C | A | 1 | a0001c0001t0001g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.91-5829C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812382 | ||||||
| chr20:50812382
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.91-5829C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812382 | ||||||
| chr20:50812399
|
A | G | 1 | a0002c0002t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.91-5812A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812399 | ||||||
| chr20:50812420
|
T | C | 1 | a0001c0001t0001g0143 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.91-5791T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812420 | ||||||
| chr20:50812449
|
TA | T | 12 | a0001c0003t0001g0004a0001c0003t0001g0005a0001c0004t0001g0012others(9): Show | 12 | HG01123.hp1 HG01346.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-5759delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50812449 | |||||
| chr20:50812450
|
A | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(117): Show | 120 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.91-5761A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812450 | ||||||
| chr20:50812477
|
C | T | 3 | a0002c0002t0001g0019a0002c0002t0001g0028a0002c0002t0003g0053 | 3 | NA18950.hp2 NA19009.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.91-5734C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812477 | ||||||
| chr20:50812536
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.91-5675C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812536 | ||||||
| chr20:50812542
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91-5669C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812542 | ||||||
| chr20:50812597
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.91-5614G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812597 | ||||||
| chr20:50812602
|
G | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0188 | 2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.91-5609G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812602 | ||||||
| chr20:50812877
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.91-5334G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812877 | ||||||
| chr20:50812946
|
G | T | 3 | a0001c0003t0001g0004a0001c0003t0001g0005a0002c0002t0003g0038 | 3 | HG02280.hp2 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.91-5265G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812946 | ||||||
| chr20:50812976
|
C | T | 5 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0003g0065others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-5235C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50812976 | ||||||
| chr20:50813110
|
T | C | 92 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(89): Show | 92 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.91-5101T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50813110 | ||||||
| chr20:50813266
|
G | A | 32 | a0001c0001t0003g0239a0001c0001t0006g0077a0002c0002t0001g0023others(29): Show | 32 | HG00408.hp1 HG01123.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.91-4945G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50813266 | ||||||
| chr20:50813359
|
T | C | 3 | a0002c0002t0001g0019a0002c0002t0001g0028a0002c0002t0003g0053 | 3 | NA18950.hp2 NA19009.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.91-4852T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50813359 | ||||||
| chr20:50813671
|
G | A | 2 | a0001c0001t0001g0167a0001c0001t0001g0188 | 2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.91-4540G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50813671 | ||||||
| chr20:50813674
|
C | CT | 28 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0143others(25): Show | 28 | HG00408.hp1 HG00558.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.91-4512dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50813674 | |||||
| chr20:50813674
|
C | CTT | 11 | a0001c0001t0001g0198a0001c0001t0001g0212a0001c0001t0003g0223others(8): Show | 11 | HG00423.hp1 HG01167.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.91-4513_91-4512dup others(2): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50813674 | |||||
| chr20:50813674
|
C | CTTT | 61 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0228others(58): Show | 61 | HG00609.hp1 HG00621.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.91-4514_91-4512dup others(3): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50813674 | |||||
| chr20:50813674
|
C | CTTTT | 21 | a0001c0001t0001g0075a0001c0001t0001g0237a0001c0001t0001g0256others(18): Show | 21 | HG00735.hp1 HG01358.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.91-4515_91-4512dup others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50813674 | |||||
| chr20:50813674
|
CT | C | 9 | a0001c0001t0001g0144a0001c0001t0002g0017a0001c0001t0002g0141others(6): Show | 9 | HG01074.hp1 HG01167.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.91-4512delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50813674 | |||||
| chr20:50813755
|
G | T | 37 | a0001c0001t0001g0001a0001c0001t0003g0239a0001c0001t0006g0077others(34): Show | 37 | HG00408.hp1 HG01123.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.91-4456G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50813755 | ||||||
| chr20:50813800
|
A | G | 1 | a0001c0001t0002g0076 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.91-4411A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50813800 | ||||||
| chr20:50813891
|
A | G | 3 | a0001c0003t0001g0004a0001c0003t0001g0005a0002c0002t0003g0038 | 3 | HG02280.hp2 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.91-4320A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50813891 | ||||||
| chr20:50814109
|
G | A | 1 | a0002c0002t0003g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.91-4102G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814109 | ||||||
| chr20:50814157
|
A | C | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91-4054A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814157 | ||||||
| chr20:50814221
|
G | A | 85 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(82): Show | 85 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.91-3990G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814221 | ||||||
| chr20:50814231
|
G | T | 1 | a0001c0001t0001g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.91-3980G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814231 | ||||||
| chr20:50814251
|
C | A | 5 | a0001c0001t0001g0198a0001c0001t0002g0225a0001c0001t0002g0226others(2): Show | 5 | HG00423.hp1 HG00621.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-3960C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814251 | ||||||
| chr20:50814378
|
T | C | 86 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(83): Show | 86 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.91-3833T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814378 | ||||||
| chr20:50814388
|
T | G | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.91-3823T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814388 | ||||||
| chr20:50814447
|
C | T | 5 | a0003c0005t0002g0078a0003c0005t0002g0128a0003c0005t0006g0082others(2): Show | 5 | HG01361.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-3764C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814447 | ||||||
| chr20:50814524
|
A | T | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.91-3687A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814524 | ||||||
| chr20:50814635
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0003g0239a0001c0001t0006g0077others(39): Show | 42 | HG00408.hp1 HG01123.hp1 HG01346.hp1 others(39): Show |
intron_variant | MODIFIER | c.91-3576C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814635 | ||||||
| chr20:50814677
|
A | C | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91-3534A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814677 | ||||||
| chr20:50814726
|
GAA | G | 5 | a0001c0004t0001g0012a0001c0004t0002g0015a0001c0004t0002g0016others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-3483_91-3482del others(2): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50814726 | |||||
| chr20:50814730
|
T | G | 5 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0003g0065others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-3481T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814730 | ||||||
| chr20:50814840
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.91-3371G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814840 | ||||||
| chr20:50814979
|
G | A | 4 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0229others(1): Show | 4 | NA18966.hp1 NA18968.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.91-3232G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50814979 | ||||||
| chr20:50815208
|
G | C | 1 | a0001c0001t0004g0235 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.91-3003G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50815208 | ||||||
| chr20:50815347
|
A | C | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91-2864A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50815347 | ||||||
| chr20:50815376
|
G | T | 85 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(82): Show | 85 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.91-2835G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50815376 | ||||||
| chr20:50815377
|
T | G | 85 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(82): Show | 85 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.91-2834T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50815377 | ||||||
| chr20:50815614
|
G | A | 1 | a0001c0001t0002g0213 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.91-2597G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50815614 | ||||||
| chr20:50815846
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.91-2365C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50815846 | ||||||
| chr20:50815866
|
C | T | 78 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(75): Show | 78 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.91-2345C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50815866 | ||||||
| chr20:50816021
|
C | A | 3 | a0001c0001t0001g0131a0001c0001t0001g0134a0001c0001t0001g0145 | 3 | HG01192.hp2 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.91-2190C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50816021 | ||||||
| chr20:50816137
|
T | TGCCTCAG others(592): Show |
28 | a0001c0001t0001g0001a0001c0001t0003g0239a0001c0001t0006g0077others(25): Show | 28 | HG00408.hp1 HG01123.hp1 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.91-2059_91-1461dup others(599): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50816137 | |||||
| chr20:50816199
|
T | C | 7 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0002g0174others(4): Show | 7 | HG01167.hp2 HG01261.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.91-2012T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50816199 | ||||||
| chr20:50816305
|
C | T | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91-1906C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50816305 | ||||||
| chr20:50816308
|
G | A | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91-1903G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50816308 | ||||||
| chr20:50816312
|
C | T | 5 | a0001c0001t0001g0198a0001c0001t0002g0225a0001c0001t0002g0226others(2): Show | 5 | HG00423.hp1 HG00621.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-1899C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50816312 | ||||||
| chr20:50816719
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.91-1492C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50816719 | ||||||
| chr20:50816791
|
A | AT | 32 | a0001c0001t0001g0022a0001c0001t0001g0092a0001c0001t0001g0114others(29): Show | 32 | HG00423.hp2 HG00735.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.91-1389dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50816791 | |||||
| chr20:50816791
|
A | ATTTTTT | 18 | a0002c0002t0001g0019a0002c0002t0001g0023a0002c0002t0001g0024others(15): Show | 18 | HG00408.hp1 HG01943.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.91-1394_91-1389dup others(6): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50816791 | |||||
| chr20:50816791
|
A | ATTTTTTT | 15 | a0001c0001t0001g0001a0001c0001t0003g0239a0002c0002t0001g0025others(12): Show | 15 | HG01123.hp1 HG01346.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.91-1395_91-1389dup others(7): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50816791 | |||||
| chr20:50816791
|
AT | A | 18 | a0001c0001t0001g0126a0001c0001t0001g0147a0001c0001t0001g0205others(15): Show | 18 | HG00609.hp2 HG01167.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.91-1389delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50816791 | |||||
| chr20:50816791
|
ATT | A | 22 | a0001c0001t0001g0075a0001c0001t0001g0251a0001c0001t0001g0256others(19): Show | 22 | HG00735.hp1 HG01256.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.91-1390_91-1389del others(2): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50816791 | |||||
| chr20:50816791
|
ATTT | A | 64 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0198others(61): Show | 64 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.91-1391_91-1389del others(3): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50816791 | |||||
| chr20:50816791
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.91-1401_91-1389del others(13): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50816791 | |||||
| chr20:50816791
|
ATTTTTTT others(10): Show |
A | 1 | a0002c0002t0003g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.91-1405_91-1389del others(17): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50816791 | |||||
| chr20:50816897
|
C | T | 2 | a0001c0001t0002g0194a0001c0001t0002g0197 | 2 | HG02071.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.91-1314C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50816897 | ||||||
| chr20:50817047
|
C | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0028 | 2 | NA18950.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.91-1164C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817047 | ||||||
| chr20:50817048
|
G | T | 6 | a0001c0001t0001g0228a0001c0001t0001g0246a0001c0001t0001g0253others(3): Show | 6 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.91-1163G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817048 | ||||||
| chr20:50817103
|
A | AT | 7 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0270others(4): Show | 7 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.91-1093dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50817103 | |||||
| chr20:50817156
|
T | A | 3 | a0001c0001t0002g0270a0002c0002t0001g0019a0002c0002t0001g0028 | 3 | HG06807.hp1 NA18950.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.91-1055T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817156 | ||||||
| chr20:50817190
|
G | T | 11 | a0001c0001t0001g0157a0001c0001t0001g0205a0001c0001t0002g0076others(8): Show | 11 | HG00423.hp2 HG00738.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.91-1021G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817190 | ||||||
| chr20:50817239
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.91-972T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817239 | ||||||
| chr20:50817253
|
A | G | 2 | a0001c0001t0002g0103a0001c0001t0002g0268 | 2 | HG00609.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.91-958A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817253 | ||||||
| chr20:50817285
|
T | C | 3 | a0001c0003t0001g0004a0001c0003t0001g0005a0002c0002t0003g0038 | 3 | HG02280.hp2 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.91-926T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817285 | ||||||
| chr20:50817412
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.91-799C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817412 | ||||||
| chr20:50817468
|
T | C | 2 | a0001c0001t0002g0132a0001c0001t0002g0164 | 2 | NA19074.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.91-743T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817468 | ||||||
| chr20:50817610
|
C | T | 5 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0003g0065others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-601C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817610 | ||||||
| chr20:50817626
|
T | A | 1 | a0002c0002t0001g0056 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.91-585T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817626 | ||||||
| chr20:50817707
|
C | T | 5 | a0001c0001t0001g0234a0001c0004t0002g0009a0001c0004t0003g0008others(2): Show | 5 | HG02145.hp1 HG02895.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.91-504C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817707 | ||||||
| chr20:50817718
|
A | T | 1 | a0002c0002t0001g0056 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.91-493A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817718 | ||||||
| chr20:50817989
|
A | G | 88 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(85): Show | 88 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.91-222A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50817989 | ||||||
| chr20:50818084
|
G | A | 1 | a0001c0004t0001g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.91-127G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50818084 | ||||||
| chr20:50818091
|
G | A | 5 | a0001c0001t0001g0198a0001c0001t0002g0225a0001c0001t0002g0226others(2): Show | 5 | HG00423.hp1 HG00621.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.91-120G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | chr20 | 50818091 | ||||||
| chr20:50818132
|
TA | T | 90 | a0001c0001t0001g0075a0001c0001t0001g0113a0001c0001t0001g0117others(87): Show | 90 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.91-63delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr20 | 50818132 | |||||
| chr20:50818292
|
T | TGCCTGGA others(14): Show |
85 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(82): Show | 85 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.162+14_162+34dupTG others(19): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr20 | 50818292 | |||||
| chr20:50818400
|
G | A | 1 | a0001c0001t0002g0180 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.162+118G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50818400 | ||||||
| chr20:50818439
|
C | CCT | 11 | a0001c0001t0001g0001a0001c0001t0001g0198a0001c0001t0002g0225others(8): Show | 11 | HG00423.hp1 HG00621.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+171_162+172dup others(2): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr20 | 50818439 | |||||
| chr20:50818660
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.162+378T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50818660 | ||||||
| chr20:50818729
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.162+447G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50818729 | ||||||
| chr20:50818788
|
C | G | 85 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(82): Show | 85 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.162+506C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50818788 | ||||||
| chr20:50818810
|
A | T | 1 | a0002c0002t0002g0041 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.162+528A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50818810 | ||||||
| chr20:50818949
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(134): Show | 137 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.162+667A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50818949 | ||||||
| chr20:50818951
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(134): Show | 137 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.162+669A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50818951 | ||||||
| chr20:50818953
|
C | T | 3 | a0001c0003t0001g0004a0001c0003t0001g0005a0002c0002t0003g0038 | 3 | HG02280.hp2 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.162+671C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50818953 | ||||||
| chr20:50818954
|
G | A | 5 | a0001c0004t0001g0012a0001c0004t0002g0015a0001c0004t0002g0016others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+672G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50818954 | ||||||
| chr20:50819054
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.162+772G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819054 | ||||||
| chr20:50819062
|
A | T | 1 | a0001c0001t0003g0002 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162+780A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819062 | ||||||
| chr20:50819072
|
A | G | 3 | a0002c0002t0001g0019a0002c0002t0001g0028a0002c0002t0003g0053 | 3 | NA18950.hp2 NA19009.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.162+790A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819072 | ||||||
| chr20:50819108
|
G | A | 29 | a0001c0001t0001g0001a0001c0001t0003g0239a0001c0001t0006g0077others(26): Show | 29 | HG00408.hp1 HG01123.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.162+826G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819108 | ||||||
| chr20:50819162
|
G | A | 1 | a0002c0002t0001g0031 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.162+880G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819162 | ||||||
| chr20:50819182
|
C | CA | 7 | a0001c0001t0003g0243a0001c0003t0001g0004a0001c0003t0001g0005others(4): Show | 7 | HG02280.hp2 HG02717.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+910dupA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr20 | 50819182 | |||||
| chr20:50819193
|
G | A | 77 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(74): Show | 77 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.162+911G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819193 | ||||||
| chr20:50819367
|
A | G | 78 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(75): Show | 78 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.162+1085A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819367 | ||||||
| chr20:50819369
|
T | C | 78 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(75): Show | 78 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.162+1087T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819369 | ||||||
| chr20:50819505
|
A | G | 1 | a0001c0003t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.162+1223A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819505 | ||||||
| chr20:50819545
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.162+1263G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819545 | ||||||
| chr20:50819586
|
A | G | 78 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(75): Show | 78 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.162+1304A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819586 | ||||||
| chr20:50819597
|
G | A | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.162+1315G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819597 | ||||||
| chr20:50819634
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.162+1352C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819634 | ||||||
| chr20:50819650
|
G | T | 1 | a0002c0002t0002g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.162+1368G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819650 | ||||||
| chr20:50819749
|
C | T | 3 | a0001c0001t0005g0221a0001c0001t0005g0250a0001c0001t0005g0255 | 3 | HG00642.hp1 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.162+1467C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819749 | ||||||
| chr20:50819787
|
TGTCTTTC others(9): Show |
T | 37 | a0001c0001t0001g0001a0001c0001t0003g0239a0001c0001t0006g0077others(34): Show | 37 | HG00408.hp1 HG01123.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.162+1529_162+1544d others(18): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr20 | 50819787 | |||||
| chr20:50819804
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0002g0090a0001c0001t0002g0097others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+1522G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819804 | ||||||
| chr20:50819811
|
TGTCTTTC others(1): Show |
T | 6 | a0001c0001t0003g0002a0003c0005t0002g0078a0003c0005t0002g0128others(3): Show | 6 | HG01361.hp2 HG02055.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+1538_162+1545d others(10): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr20 | 50819811 | |||||
| chr20:50819868
|
C | T | 1 | a0002c0002t0002g0020 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.162+1586C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819868 | ||||||
| chr20:50819906
|
C | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0075others(248): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.162+1624C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50819906 | ||||||
| chr20:50820054
|
GCTGGT | G | 78 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(75): Show | 78 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.162+1775_162+1779d others(7): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr20 | 50820054 | |||||
| chr20:50820114
|
A | G | 4 | a0001c0001t0002g0074a0001c0001t0002g0211a0001c0001t0003g0227others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+1832A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50820114 | ||||||
| chr20:50820177
|
G | A | 2 | a0002c0002t0002g0041a0002c0002t0002g0046 | 2 | HG00408.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.162+1895G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50820177 | ||||||
| chr20:50820413
|
A | G | 2 | a0001c0001t0001g0252a0001c0001t0003g0254 | 2 | HG00609.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.162+2131A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50820413 | ||||||
| chr20:50820531
|
A | G | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.162+2249A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50820531 | ||||||
| chr20:50820622
|
C | T | 1 | a0002c0002t0001g0024 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.162+2340C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50820622 | ||||||
| chr20:50820688
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.162+2406A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50820688 | ||||||
| chr20:50820905
|
GA | G | 5 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0003g0065others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+2629delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr20 | 50820905 | |||||
| chr20:50821035
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0003g0239a0001c0001t0006g0077others(33): Show | 36 | HG00408.hp1 HG01123.hp1 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.162+2753C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50821035 | ||||||
| chr20:50821472
|
C | T | 10 | a0001c0001t0001g0198a0001c0001t0002g0225a0001c0001t0002g0226others(7): Show | 10 | HG00423.hp1 HG00621.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+3190C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50821472 | ||||||
| chr20:50821491
|
C | G | 10 | a0001c0001t0001g0198a0001c0001t0002g0225a0001c0001t0002g0226others(7): Show | 10 | HG00423.hp1 HG00621.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.162+3209C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50821491 | ||||||
| chr20:50821520
|
G | C | 5 | a0001c0001t0003g0239a0002c0002t0001g0055a0002c0002t0001g0056others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+3238G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50821520 | ||||||
| chr20:50821580
|
G | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.162+3298G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50821580 | ||||||
| chr20:50822636
|
G | GT | 13 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0198others(10): Show | 13 | HG00423.hp1 HG00735.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.162+4370dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr20 | 50822636 | |||||
| chr20:50822738
|
C | T | 6 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0003g0223others(3): Show | 6 | HG01167.hp2 HG01261.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+4456C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50822738 | ||||||
| chr20:50822783
|
C | T | 5 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0003g0065others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+4501C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50822783 | ||||||
| chr20:50822784
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.162+4502G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50822784 | ||||||
| chr20:50822842
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(134): Show | 137 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.162+4560G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50822842 | ||||||
| chr20:50823066
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.162+4784G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50823066 | ||||||
| chr20:50823078
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.162+4796G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50823078 | ||||||
| chr20:50823110
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162+4828C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50823110 | ||||||
| chr20:50823271
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.162+4989C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50823271 | ||||||
| chr20:50823272
|
G | A | 1 | a0001c0001t0002g0170 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.162+4990G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50823272 | ||||||
| chr20:50823316
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0140 | 2 | HG01074.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.162+5034G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50823316 | ||||||
| chr20:50823342
|
C | T | 3 | a0002c0002t0001g0019a0002c0002t0001g0028a0002c0002t0003g0053 | 3 | NA18950.hp2 NA19009.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.162+5060C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50823342 | ||||||
| chr20:50823608
|
G | T | 7 | a0001c0001t0001g0179a0001c0001t0002g0124a0001c0001t0002g0138others(4): Show | 7 | HG00558.hp2 HG01952.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+5326G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50823608 | ||||||
| chr20:50823630
|
TG | T | 3 | a0002c0002t0001g0019a0002c0002t0001g0028a0002c0002t0003g0053 | 3 | NA18950.hp2 NA19009.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.162+5351delG | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr20 | 50823630 | |||||
| chr20:50823717
|
C | G | 1 | a0001c0004t0002g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.162+5435C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50823717 | ||||||
| chr20:50823717
|
C | T | 2 | a0001c0001t0002g0071a0001c0001t0002g0072 | 2 | HG02572.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.162+5435C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50823717 | ||||||
| chr20:50823889
|
G | A | 1 | a0002c0002t0003g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.162+5607G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50823889 | ||||||
| chr20:50824018
|
A | G | 3 | a0001c0003t0001g0004a0001c0003t0001g0005a0002c0002t0003g0038 | 3 | HG02280.hp2 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.162+5736A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824018 | ||||||
| chr20:50824126
|
G | A | 5 | a0001c0004t0001g0012a0001c0004t0002g0015a0001c0004t0002g0016others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.162+5844G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824126 | ||||||
| chr20:50824167
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.162+5885G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824167 | ||||||
| chr20:50824240
|
G | C | 3 | a0001c0001t0001g0168a0001c0001t0002g0119a0005c0007t0002g0150 | 3 | HG02523.hp1 NA18968.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.162+5958G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824240 | ||||||
| chr20:50824544
|
G | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(132): Show | 135 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.163-5735G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824544 | ||||||
| chr20:50824550
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163-5729T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824550 | ||||||
| chr20:50824573
|
C | T | 5 | a0001c0004t0001g0012a0001c0004t0002g0015a0001c0004t0002g0016others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-5706C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824573 | ||||||
| chr20:50824579
|
A | T | 79 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(76): Show | 79 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.163-5700A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824579 | ||||||
| chr20:50824725
|
G | A | 5 | a0001c0004t0001g0012a0001c0004t0002g0015a0001c0004t0002g0016others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-5554G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824725 | ||||||
| chr20:50824738
|
G | A | 3 | a0001c0003t0001g0004a0001c0003t0001g0005a0002c0002t0003g0038 | 3 | HG02280.hp2 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.163-5541G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824738 | ||||||
| chr20:50824825
|
C | T | 89 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(86): Show | 89 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.163-5454C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824825 | ||||||
| chr20:50824914
|
T | C | 29 | a0001c0001t0001g0001a0001c0001t0003g0239a0001c0001t0006g0077others(26): Show | 29 | HG00408.hp1 HG01123.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.163-5365T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50824914 | ||||||
| chr20:50825103
|
A | G | 37 | a0001c0001t0001g0001a0001c0001t0003g0239a0001c0001t0006g0077others(34): Show | 37 | HG00408.hp1 HG01123.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.163-5176A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50825103 | ||||||
| chr20:50825329
|
A | G | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163-4950A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50825329 | ||||||
| chr20:50825333
|
C | T | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.163-4946C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50825333 | ||||||
| chr20:50825388
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.163-4891T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50825388 | ||||||
| chr20:50825469
|
C | G | 1 | a0001c0001t0007g0265 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.163-4810C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50825469 | ||||||
| chr20:50825651
|
A | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(134): Show | 137 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.163-4628A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50825651 | ||||||
| chr20:50825711
|
T | C | 1 | a0001c0001t0002g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.163-4568T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50825711 | ||||||
| chr20:50825741
|
G | A | 1 | a0001c0001t0004g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.163-4538G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50825741 | ||||||
| chr20:50825812
|
G | T | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163-4467G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50825812 | ||||||
| chr20:50825941
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(133): Show | 136 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(133): Show |
intron_variant | MODIFIER | c.163-4338A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50825941 | ||||||
| chr20:50826025
|
A | G | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163-4254A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50826025 | ||||||
| chr20:50826118
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0173others(132): Show | 135 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.163-4161C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50826118 | ||||||
| chr20:50826187
|
T | G | 1 | a0002c0002t0003g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.163-4092T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50826187 | ||||||
| chr20:50826388
|
C | T | 3 | a0001c0003t0001g0004a0001c0003t0001g0005a0002c0002t0003g0038 | 3 | HG02280.hp2 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.163-3891C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50826388 | ||||||
| chr20:50826686
|
A | G | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.163-3593A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50826686 | ||||||
| chr20:50826995
|
G | A | 2 | a0001c0001t0001g0120a0002c0002t0001g0042 | 2 | HG00558.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.163-3284G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50826995 | ||||||
| chr20:50827015
|
C | CA | 10 | a0001c0001t0001g0198a0001c0001t0002g0225a0001c0001t0002g0226others(7): Show | 10 | HG00423.hp1 HG00621.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-3261dupA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr20 | 50827015 | |||||
| chr20:50827027
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.163-3252C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827027 | ||||||
| chr20:50827102
|
T | G | 1 | a0002c0002t0003g0053 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.163-3177T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827102 | ||||||
| chr20:50827311
|
T | C | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163-2968T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827311 | ||||||
| chr20:50827425
|
C | T | 85 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(82): Show | 85 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.163-2854C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827425 | ||||||
| chr20:50827559
|
T | C | 36 | a0001c0001t0001g0102a0001c0001t0001g0198a0001c0001t0002g0225others(33): Show | 36 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.163-2720T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827559 | ||||||
| chr20:50827573
|
G | A | 2 | a0002c0002t0001g0019a0002c0002t0001g0028 | 2 | NA18950.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.163-2706G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827573 | ||||||
| chr20:50827579
|
T | C | 5 | a0001c0004t0001g0012a0001c0004t0002g0015a0001c0004t0002g0016others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2700T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827579 | ||||||
| chr20:50827620
|
C | T | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.163-2659C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827620 | ||||||
| chr20:50827766
|
G | T | 7 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0270others(4): Show | 7 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-2513G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827766 | ||||||
| chr20:50827798
|
C | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0177others(1): Show | 4 | HG00099.hp2 HG01070.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2481C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827798 | ||||||
| chr20:50827811
|
C | T | 4 | a0001c0001t0002g0074a0001c0001t0002g0211a0001c0001t0003g0227others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2468C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827811 | ||||||
| chr20:50827825
|
T | C | 1 | a0002c0002t0004g0061 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.163-2454T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827825 | ||||||
| chr20:50827875
|
C | T | 5 | a0001c0004t0001g0012a0001c0004t0002g0015a0001c0004t0002g0016others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2404C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827875 | ||||||
| chr20:50827876
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.163-2403G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827876 | ||||||
| chr20:50827937
|
T | C | 3 | a0001c0001t0005g0221a0001c0001t0005g0250a0001c0001t0005g0255 | 3 | HG00642.hp1 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.163-2342T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827937 | ||||||
| chr20:50827942
|
A | G | 2 | a0002c0002t0001g0037a0002c0002t0003g0045 | 2 | NA18965.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.163-2337A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50827942 | ||||||
| chr20:50828024
|
G | A | 1 | a0001c0001t0004g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.163-2255G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828024 | ||||||
| chr20:50828036
|
T | A | 13 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(10): Show | 13 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.163-2243T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828036 | ||||||
| chr20:50828037
|
T | A | 5 | a0001c0001t0002g0225a0001c0001t0002g0226a0003c0005t0002g0128others(2): Show | 5 | HG01884.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-2242T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828037 | ||||||
| chr20:50828072
|
G | A | 2 | a0002c0002t0001g0019a0002c0002t0001g0028 | 2 | NA18950.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.163-2207G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828072 | ||||||
| chr20:50828202
|
G | A | 1 | a0002c0002t0003g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.163-2077G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828202 | ||||||
| chr20:50828211
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.163-2068G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828211 | ||||||
| chr20:50828246
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.163-2033G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828246 | ||||||
| chr20:50828290
|
G | A | 1 | a0001c0003t0001g0108 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.163-1989G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828290 | ||||||
| chr20:50828350
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.163-1929G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828350 | ||||||
| chr20:50828394
|
G | A | 1 | a0002c0002t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.163-1885G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828394 | ||||||
| chr20:50828459
|
G | C | 7 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0270others(4): Show | 7 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-1820G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828459 | ||||||
| chr20:50828609
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.163-1670G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828609 | ||||||
| chr20:50828710
|
C | T | 2 | a0001c0003t0001g0004a0001c0003t0001g0005 | 2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.163-1569C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828710 | ||||||
| chr20:50828870
|
G | A | 6 | a0001c0001t0002g0017a0001c0004t0001g0012a0001c0004t0002g0015others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-1409G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828870 | ||||||
| chr20:50828909
|
C | T | 77 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(74): Show | 77 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.163-1370C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50828909 | ||||||
| chr20:50829055
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.163-1224A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50829055 | ||||||
| chr20:50829523
|
G | A | 2 | a0001c0004t0003g0008a0001c0004t0004g0007 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.163-756G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50829523 | ||||||
| chr20:50829822
|
C | T | 9 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(6): Show | 9 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.163-457C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50829822 | ||||||
| chr20:50829829
|
A | G | 8 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0270others(5): Show | 8 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.163-450A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50829829 | ||||||
| chr20:50829839
|
T | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(113): Show | 116 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.163-440T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50829839 | ||||||
| chr20:50829895
|
T | C | 15 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.163-384T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50829895 | ||||||
| chr20:50830041
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(136): Show | 139 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.163-238T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50830041 | ||||||
| chr20:50830069
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.163-210C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50830069 | ||||||
| chr20:50830093
|
C | G | 5 | a0001c0004t0001g0012a0001c0004t0002g0015a0001c0004t0002g0016others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-186C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50830093 | ||||||
| chr20:50830154
|
C | T | 16 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(13): Show | 16 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-125C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 2/4 | chr20 | 50830154 | ||||||
| chr20:50830385
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | splice_region_variant&intron_variant | LOW | c.264+5G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50830385 | ||||||
| chr20:50830410
|
C | T | 8 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0270others(5): Show | 8 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.264+30C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50830410 | ||||||
| chr20:50830441
|
G | A | 2 | a0001c0001t0002g0174a0001c0001t0004g0099 | 2 | HG02572.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.264+61G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50830441 | ||||||
| chr20:50830514
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.264+134G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50830514 | ||||||
| chr20:50830538
|
A | G | 8 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0270others(5): Show | 8 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.264+158A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50830538 | ||||||
| chr20:50830555
|
A | G | 8 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0270others(5): Show | 8 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.264+175A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50830555 | ||||||
| chr20:50830791
|
T | C | 28 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(25): Show | 28 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.264+411T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50830791 | ||||||
| chr20:50831017
|
C | G | 7 | a0001c0001t0001g0234a0001c0001t0002g0074a0001c0001t0002g0211others(4): Show | 7 | HG02145.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.264+637C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50831017 | ||||||
| chr20:50831222
|
A | G | 9 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(6): Show | 9 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.264+842A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50831222 | ||||||
| chr20:50831224
|
T | C | 12 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0110others(9): Show | 12 | HG00738.hp2 HG01071.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.264+844T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50831224 | ||||||
| chr20:50831419
|
G | A | 23 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(20): Show | 23 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.264+1039G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50831419 | ||||||
| chr20:50831540
|
T | C | 1 | a0002c0002t0002g0046 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.264+1160T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50831540 | ||||||
| chr20:50831559
|
G | A | 5 | a0001c0004t0001g0012a0001c0004t0002g0015a0001c0004t0002g0016others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+1179G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50831559 | ||||||
| chr20:50831579
|
T | C | 23 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(20): Show | 23 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.264+1199T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50831579 | ||||||
| chr20:50831793
|
C | T | 5 | a0001c0004t0001g0012a0001c0004t0002g0015a0001c0004t0002g0016others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+1413C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50831793 | ||||||
| chr20:50831863
|
G | A | 7 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0270others(4): Show | 7 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+1483G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50831863 | ||||||
| chr20:50831915
|
T | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(33): Show | 36 | HG00408.hp1 HG01123.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.264+1535T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50831915 | ||||||
| chr20:50832058
|
G | A | 8 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0270others(5): Show | 8 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.264+1678G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50832058 | ||||||
| chr20:50832114
|
C | A | 2 | a0001c0001t0002g0257a0001c0001t0002g0269 | 2 | HG00741.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.264+1734C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50832114 | ||||||
| chr20:50832203
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.264+1823A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50832203 | ||||||
| chr20:50832263
|
C | CT | 23 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(20): Show | 23 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.264+1896dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50832263 | |||||
| chr20:50832414
|
C | T | 2 | a0001c0001t0002g0216a0001c0001t0002g0217 | 2 | HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.264+2034C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50832414 | ||||||
| chr20:50832439
|
G | A | 13 | a0001c0001t0002g0192a0001c0001t0002g0213a0001c0001t0002g0215others(10): Show | 13 | HG00741.hp1 HG01106.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.264+2059G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50832439 | ||||||
| chr20:50832501
|
G | A | 1 | a0001c0001t0002g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.264+2121G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50832501 | ||||||
| chr20:50832504
|
C | T | 2 | a0001c0001t0002g0270a0002c0002t0003g0057 | 2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.264+2124C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50832504 | ||||||
| chr20:50832619
|
G | C | 3 | a0002c0002t0001g0033a0002c0002t0001g0039a0002c0002t0004g0061 | 3 | HG03942.hp2 HG04199.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.264+2239G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50832619 | ||||||
| chr20:50832848
|
C | G | 1 | a0001c0001t0001g0001 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.264+2468C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50832848 | ||||||
| chr20:50832926
|
G | A | 9 | a0001c0001t0001g0238a0001c0001t0001g0252a0001c0001t0003g0209others(6): Show | 9 | HG00609.hp1 HG01978.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.264+2546G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50832926 | ||||||
| chr20:50832957
|
A | T | 15 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.264+2577A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50832957 | ||||||
| chr20:50833241
|
G | A | 1 | a0001c0003t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.264+2861G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50833241 | ||||||
| chr20:50833343
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(36): Show | 39 | HG00408.hp1 HG01123.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.264+2963G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50833343 | ||||||
| chr20:50833392
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(136): Show | 139 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.264+3012A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50833392 | ||||||
| chr20:50833439
|
G | A | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.264+3059G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50833439 | ||||||
| chr20:50833439
|
G | C | 7 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0270others(4): Show | 7 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+3059G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50833439 | ||||||
| chr20:50833590
|
G | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0002g0189others(1): Show | 4 | HG00639.hp1 HG01258.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+3210G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50833590 | ||||||
| chr20:50833598
|
A | G | 2 | a0001c0001t0002g0270a0002c0002t0003g0057 | 2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.264+3218A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50833598 | ||||||
| chr20:50833659
|
A | G | 7 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0270others(4): Show | 7 | HG02572.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+3279A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50833659 | ||||||
| chr20:50833712
|
A | G | 22 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(19): Show | 22 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.264+3332A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50833712 | ||||||
| chr20:50834009
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.264+3629C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50834009 | ||||||
| chr20:50834068
|
G | C | 77 | a0001c0001t0001g0075a0001c0001t0001g0173a0001c0001t0001g0175others(74): Show | 77 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.264+3688G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50834068 | ||||||
| chr20:50834076
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.264+3696G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50834076 | ||||||
| chr20:50834222
|
C | G | 14 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(11): Show | 14 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.264+3842C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50834222 | ||||||
| chr20:50834226
|
C | G | 14 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(11): Show | 14 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.264+3846C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50834226 | ||||||
| chr20:50834292
|
C | CT | 21 | a0001c0001t0001g0075a0001c0001t0001g0143a0001c0001t0001g0145others(18): Show | 21 | HG01192.hp1 HG01192.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.264+3933dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50834292 | |||||
| chr20:50834292
|
C | CTTT | 8 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(5): Show | 8 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.264+3931_264+3933d others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50834292 | |||||
| chr20:50834292
|
CT | C | 10 | a0001c0001t0001g0109a0001c0001t0001g0266a0001c0001t0002g0146others(7): Show | 10 | HG01256.hp1 HG01975.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.264+3933delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50834292 | |||||
| chr20:50834292
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0087a0001c0001t0003g0073 | 2 | HG02273.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.264+3923_264+3933d others(13): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50834292 | |||||
| chr20:50834652
|
T | C | 20 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(17): Show | 20 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.264+4272T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50834652 | ||||||
| chr20:50834872
|
G | T | 73 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0001g0228others(70): Show | 73 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.264+4492G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50834872 | ||||||
| chr20:50835020
|
C | T | 1 | a0001c0001t0002g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264+4640C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50835020 | ||||||
| chr20:50835245
|
A | AT | 44 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0173others(41): Show | 44 | HG00408.hp1 HG00642.hp1 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.264+4883dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50835245 | |||||
| chr20:50835245
|
A | ATT | 57 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0001g0228others(54): Show | 57 | HG00609.hp1 HG00735.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.264+4882_264+4883d others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50835245 | |||||
| chr20:50835245
|
A | ATTT | 11 | a0001c0001t0002g0086a0001c0001t0003g0240a0001c0001t0003g0241others(8): Show | 11 | HG01256.hp1 HG01433.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.264+4881_264+4883d others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50835245 | |||||
| chr20:50835245
|
ATT | A | 15 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.264+4882_264+4883d others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50835245 | |||||
| chr20:50835389
|
C | T | 37 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0173others(34): Show | 37 | HG00408.hp1 HG00639.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.264+5009C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50835389 | ||||||
| chr20:50835523
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0125a0001c0001t0002g0141 | 3 | HG01074.hp1 HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.264+5143C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50835523 | ||||||
| chr20:50835705
|
C | A | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.264+5325C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50835705 | ||||||
| chr20:50835706
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.264+5326G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50835706 | ||||||
| chr20:50835734
|
A | C | 14 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(11): Show | 14 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.264+5354A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50835734 | ||||||
| chr20:50835956
|
C | T | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.264+5576C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50835956 | ||||||
| chr20:50835989
|
C | G | 1 | a0001c0001t0001g0259 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.264+5609C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50835989 | ||||||
| chr20:50836013
|
G | A | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.264+5633G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836013 | ||||||
| chr20:50836063
|
G | C | 3 | a0001c0001t0002g0090a0001c0001t0002g0097a0001c0001t0005g0115 | 3 | HG00639.hp2 HG01243.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.264+5683G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836063 | ||||||
| chr20:50836064
|
C | T | 6 | a0001c0001t0002g0017a0001c0004t0001g0012a0001c0004t0002g0015others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+5684C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836064 | ||||||
| chr20:50836108
|
G | A | 1 | a0001c0001t0004g0098 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.265-5658G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836108 | ||||||
| chr20:50836195
|
C | T | 5 | a0003c0005t0002g0078a0003c0005t0002g0128a0003c0005t0006g0082others(2): Show | 5 | HG01361.hp2 HG02055.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-5571C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836195 | ||||||
| chr20:50836205
|
T | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(39): Show | 42 | HG00408.hp1 HG00639.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.265-5561T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836205 | ||||||
| chr20:50836213
|
G | T | 7 | a0001c0001t0002g0074a0001c0001t0002g0192a0001c0001t0002g0213others(4): Show | 7 | HG02630.hp2 HG02922.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.265-5553G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836213 | ||||||
| chr20:50836403
|
A | G | 15 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.265-5363A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836403 | ||||||
| chr20:50836453
|
C | A | 14 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(11): Show | 14 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.265-5313C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836453 | ||||||
| chr20:50836551
|
A | C | 2 | a0002c0002t0002g0020a0002c0002t0002g0021 | 2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.265-5215A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836551 | ||||||
| chr20:50836734
|
C | CT | 15 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.265-5024dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50836734 | |||||
| chr20:50836799
|
C | T | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.265-4967C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836799 | ||||||
| chr20:50836832
|
C | T | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.265-4934C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836832 | ||||||
| chr20:50836947
|
A | G | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.265-4819A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50836947 | ||||||
| chr20:50837125
|
A | G | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.265-4641A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837125 | ||||||
| chr20:50837352
|
C | T | 10 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0162others(7): Show | 10 | HG01243.hp2 HG01358.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.265-4414C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837352 | ||||||
| chr20:50837353
|
G | A | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.265-4413G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837353 | ||||||
| chr20:50837377
|
A | C | 71 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0001g0228others(68): Show | 71 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.265-4389A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837377 | ||||||
| chr20:50837389
|
T | C | 1 | a0001c0001t0008g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.265-4377T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837389 | ||||||
| chr20:50837490
|
C | T | 14 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(11): Show | 14 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.265-4276C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837490 | ||||||
| chr20:50837594
|
T | G | 14 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(11): Show | 14 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.265-4172T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837594 | ||||||
| chr20:50837634
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.265-4132T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837634 | ||||||
| chr20:50837657
|
G | A | 3 | a0001c0001t0001g0120a0002c0002t0002g0018a0002c0002t0003g0050 | 3 | HG00558.hp1 HG02027.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.265-4109G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837657 | ||||||
| chr20:50837807
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.265-3959A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837807 | ||||||
| chr20:50837830
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.265-3936G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837830 | ||||||
| chr20:50837872
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.265-3894G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837872 | ||||||
| chr20:50837983
|
C | T | 15 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.265-3783C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50837983 | ||||||
| chr20:50837999
|
T | TAC | 10 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0001g0140others(7): Show | 10 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.265-3745_265-3744d others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50837999 | |||||
| chr20:50837999
|
TAC | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(111): Show | 114 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.265-3745_265-3744d others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50837999 | |||||
| chr20:50838027
|
G | A | 1 | a0002c0002t0001g0024 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.265-3739G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838027 | ||||||
| chr20:50838065
|
C | T | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.265-3701C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838065 | ||||||
| chr20:50838084
|
C | T | 2 | a0001c0001t0007g0262a0001c0001t0007g0265 | 2 | HG01071.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.265-3682C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838084 | ||||||
| chr20:50838179
|
A | G | 2 | a0001c0001t0004g0098a0001c0001t0004g0195 | 2 | HG01952.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.265-3587A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838179 | ||||||
| chr20:50838286
|
A | C | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.265-3480A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838286 | ||||||
| chr20:50838307
|
A | G | 3 | a0002c0002t0001g0019a0002c0002t0001g0028a0006c0009t0001g0010 | 3 | NA18950.hp2 NA18973.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.265-3459A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838307 | ||||||
| chr20:50838367
|
G | A | 1 | a0001c0003t0001g0096 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.265-3399G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838367 | ||||||
| chr20:50838374
|
G | A | 3 | a0001c0001t0002g0129a0001c0001t0002g0135a0001c0001t0002g0155 | 3 | HG00099.hp1 HG00741.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.265-3392G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838374 | ||||||
| chr20:50838419
|
A | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(54): Show | 57 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.265-3347A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838419 | ||||||
| chr20:50838473
|
G | A | 1 | a0002c0002t0003g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.265-3293G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838473 | ||||||
| chr20:50838519
|
G | A | 4 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0229others(1): Show | 4 | NA18966.hp1 NA18968.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-3247G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838519 | ||||||
| chr20:50838567
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265-3199G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838567 | ||||||
| chr20:50838750
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.265-3016A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838750 | ||||||
| chr20:50838822
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.265-2944C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50838822 | ||||||
| chr20:50839145
|
C | A | 1 | a0001c0001t0003g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.265-2621C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50839145 | ||||||
| chr20:50839434
|
T | A | 1 | a0001c0001t0002g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.265-2332T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50839434 | ||||||
| chr20:50839604
|
G | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(37): Show | 40 | HG00408.hp1 HG00639.hp1 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.265-2162G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50839604 | ||||||
| chr20:50840393
|
C | T | 1 | a0002c0002t0003g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.265-1373C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840393 | ||||||
| chr20:50840451
|
T | G | 19 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(16): Show | 19 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.265-1315T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840451 | ||||||
| chr20:50840528
|
A | G | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.265-1238A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840528 | ||||||
| chr20:50840548
|
T | C | 4 | a0001c0001t0003g0240a0001c0001t0003g0241a0001c0001t0003g0242others(1): Show | 4 | HG03139.hp2 HG03579.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-1218T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840548 | ||||||
| chr20:50840571
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.265-1195A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840571 | ||||||
| chr20:50840671
|
T | G | 6 | a0001c0001t0006g0077a0001c0004t0001g0012a0001c0004t0002g0015others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-1095T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840671 | ||||||
| chr20:50840720
|
G | A | 1 | a0002c0002t0004g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.265-1046G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840720 | ||||||
| chr20:50840731
|
T | C | 1 | a0001c0001t0002g0164 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.265-1035T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840731 | ||||||
| chr20:50840732
|
A | G | 20 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(17): Show | 20 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.265-1034A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840732 | ||||||
| chr20:50840767
|
G | A | 18 | a0001c0001t0001g0238a0001c0001t0001g0245a0001c0001t0001g0249others(15): Show | 18 | HG00609.hp1 HG01167.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.265-999G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840767 | ||||||
| chr20:50840809
|
T | C | 6 | a0001c0001t0006g0077a0001c0004t0001g0012a0001c0004t0002g0015others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-957T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840809 | ||||||
| chr20:50840923
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.265-843G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840923 | ||||||
| chr20:50840971
|
G | A | 69 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0001g0228others(66): Show | 69 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.265-795G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50840971 | ||||||
| chr20:50841077
|
G | A | 1 | a0001c0001t0002g0193 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.265-689G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50841077 | ||||||
| chr20:50841181
|
C | T | 3 | a0001c0001t0001g0147a0001c0001t0002g0199a0002c0002t0003g0053 | 3 | NA19009.hp1 NA19012.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.265-585C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50841181 | ||||||
| chr20:50841216
|
C | G | 7 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(4): Show | 7 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-550C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50841216 | ||||||
| chr20:50841268
|
T | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(36): Show | 39 | HG00408.hp1 HG00639.hp1 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.265-498T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50841268 | ||||||
| chr20:50841363
|
G | C | 1 | a0001c0004t0001g0011 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.265-403G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50841363 | ||||||
| chr20:50841427
|
A | AC | 132 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(129): Show | 132 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.265-334dupC | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr20 | 50841427 | |||||
| chr20:50841526
|
A | G | 71 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0001g0228others(68): Show | 71 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.265-240A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50841526 | ||||||
| chr20:50841589
|
G | T | 2 | a0002c0002t0001g0023a0002c0002t0001g0044 | 2 | HG02056.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.265-177G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 3/4 | chr20 | 50841589 | ||||||
| chr20:50841942
|
C | G | 11 | a0001c0001t0001g0245a0001c0001t0001g0249a0001c0001t0001g0251others(8): Show | 11 | HG00408.hp1 HG01261.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.399+42C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50841942 | ||||||
| chr20:50841947
|
G | C | 40 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0107others(37): Show | 40 | HG00423.hp1 HG01074.hp2 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.399+47G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50841947 | ||||||
| chr20:50841985
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.399+85G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50841985 | ||||||
| chr20:50842039
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.399+139G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842039 | ||||||
| chr20:50842068
|
T | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(55): Show | 58 | HG00408.hp1 HG00639.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.399+168T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842068 | ||||||
| chr20:50842069
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0002g0226a0001c0001t0002g0270 | 3 | HG02630.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.399+169G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842069 | ||||||
| chr20:50842076
|
C | T | 1 | a0001c0001t0004g0202 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.399+176C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842076 | ||||||
| chr20:50842101
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(51): Show | 54 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.399+201A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842101 | ||||||
| chr20:50842304
|
C | T | 30 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0001g0234others(27): Show | 30 | HG00423.hp2 HG01256.hp1 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.399+404C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842304 | ||||||
| chr20:50842358
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+458C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842358 | ||||||
| chr20:50842361
|
T | C | 63 | a0001c0001t0001g0075a0001c0001t0001g0089a0001c0001t0001g0168others(60): Show | 63 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.399+461T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842361 | ||||||
| chr20:50842395
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.399+495G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842395 | ||||||
| chr20:50842502
|
TG | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0075others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.399+604delG | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50842502 | |||||
| chr20:50842638
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.399+738G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842638 | ||||||
| chr20:50842755
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(118): Show | 121 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(118): Show |
intron_variant | MODIFIER | c.399+855G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842755 | ||||||
| chr20:50842780
|
T | C | 1 | a0001c0001t0005g0255 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.399+880T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842780 | ||||||
| chr20:50842789
|
G | A | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.399+889G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50842789 | ||||||
| chr20:50843289
|
G | A | 25 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0001g0234others(22): Show | 25 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.399+1389G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50843289 | ||||||
| chr20:50843460
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.399+1560T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50843460 | ||||||
| chr20:50843533
|
TACCTGCC others(17): Show |
T | 11 | a0001c0001t0001g0102a0001c0001t0002g0105a0001c0001t0002g0106others(8): Show | 11 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.399+1667_399+1690d others(26): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50843533 | |||||
| chr20:50843769
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.399+1869A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50843769 | ||||||
| chr20:50843806
|
T | G | 1 | a0001c0001t0002g0158 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.399+1906T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50843806 | ||||||
| chr20:50843841
|
C | T | 31 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0001g0234others(28): Show | 31 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.399+1941C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50843841 | ||||||
| chr20:50844006
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.399+2106T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50844006 | ||||||
| chr20:50844012
|
C | T | 1 | a0002c0002t0003g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.399+2112C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50844012 | ||||||
| chr20:50844411
|
C | T | 31 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0001g0234others(28): Show | 31 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.399+2511C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50844411 | ||||||
| chr20:50844472
|
C | T | 9 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0192others(6): Show | 9 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.399+2572C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50844472 | ||||||
| chr20:50844748
|
TC | T | 108 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(105): Show | 108 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.399+2856delC | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50844748 | |||||
| chr20:50844787
|
A | C | 1 | a0001c0001t0002g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.399+2887A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50844787 | ||||||
| chr20:50844904
|
A | C | 1 | a0001c0001t0001g0001 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.399+3004A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50844904 | ||||||
| chr20:50844972
|
G | A | 5 | a0001c0001t0003g0065a0001c0001t0003g0227a0001c0001t0005g0250others(2): Show | 5 | HG02258.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+3072G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50844972 | ||||||
| chr20:50845163
|
G | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0140others(24): Show | 27 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.399+3263G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845163 | ||||||
| chr20:50845225
|
C | T | 16 | a0001c0001t0001g0089a0001c0001t0001g0107a0001c0001t0001g0140others(13): Show | 16 | HG00423.hp2 HG00621.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.399+3325C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845225 | ||||||
| chr20:50845236
|
G | A | 1 | a0002c0002t0003g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.399+3336G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845236 | ||||||
| chr20:50845261
|
A | G | 12 | a0001c0001t0002g0074a0001c0001t0002g0211a0001c0001t0002g0225others(9): Show | 12 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+3361A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845261 | ||||||
| chr20:50845276
|
G | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0107others(52): Show | 55 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.399+3376G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845276 | ||||||
| chr20:50845278
|
C | T | 68 | a0001c0001t0001g0075a0001c0001t0001g0175a0001c0001t0001g0212others(65): Show | 68 | HG00408.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.399+3378C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845278 | ||||||
| chr20:50845293
|
G | A | 1 | a0001c0003t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.399+3393G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845293 | ||||||
| chr20:50845375
|
C | G | 62 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.399+3475C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845375 | ||||||
| chr20:50845422
|
C | T | 5 | a0001c0001t0003g0065a0001c0001t0003g0227a0001c0003t0001g0133others(2): Show | 5 | HG02258.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+3522C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845422 | ||||||
| chr20:50845509
|
C | T | 1 | a0001c0001t0002g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.399+3609C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845509 | ||||||
| chr20:50845524
|
T | C | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+3624T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845524 | ||||||
| chr20:50845612
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(141): Show | 144 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.399+3712C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845612 | ||||||
| chr20:50845678
|
G | A | 1 | a0002c0002t0001g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.399+3778G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845678 | ||||||
| chr20:50845709
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0002g0151 | 2 | HG00609.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.399+3809G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845709 | ||||||
| chr20:50845747
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.399+3847G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845747 | ||||||
| chr20:50845838
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.399+3938A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845838 | ||||||
| chr20:50845850
|
A | G | 1 | a0001c0001t0003g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.399+3950A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845850 | ||||||
| chr20:50845859
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(142): Show | 145 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.399+3959A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845859 | ||||||
| chr20:50845917
|
G | A | 1 | a0001c0004t0001g0011 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.399+4017G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50845917 | ||||||
| chr20:50846009
|
C | T | 1 | a0001c0003t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.399+4109C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846009 | ||||||
| chr20:50846159
|
A | G | 1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.399+4259A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846159 | ||||||
| chr20:50846195
|
G | A | 2 | a0002c0002t0001g0023a0002c0002t0001g0044 | 2 | HG02056.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.399+4295G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846195 | ||||||
| chr20:50846368
|
T | A | 2 | a0001c0001t0002g0244a0001c0001t0002g0248 | 2 | HG02083.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.399+4468T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846368 | ||||||
| chr20:50846607
|
CT | C | 129 | a0001c0001t0001g0022a0001c0001t0001g0075a0001c0001t0001g0087others(126): Show | 129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.399+4733delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50846607 | |||||
| chr20:50846607
|
CTT | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0088a0001c0001t0001g0107others(35): Show | 38 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.399+4732_399+4733d others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50846607 | |||||
| chr20:50846607
|
CTTT | C | 11 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(8): Show | 11 | HG00423.hp2 HG01433.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.399+4731_399+4733d others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50846607 | |||||
| chr20:50846607
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.399+4721_399+4733d others(15): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50846607 | |||||
| chr20:50846609
|
T | C | 26 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0188others(23): Show | 26 | HG00408.hp1 HG01256.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.399+4709T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846609 | ||||||
| chr20:50846610
|
T | C | 4 | a0001c0001t0002g0261a0001c0001t0004g0099a0002c0002t0001g0027others(1): Show | 4 | NA18963.hp1 NA18964.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+4710T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846610 | ||||||
| chr20:50846612
|
T | C | 11 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(8): Show | 11 | HG00423.hp2 HG01433.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.399+4712T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846612 | ||||||
| chr20:50846613
|
T | C | 2 | a0001c0001t0004g0098a0002c0002t0002g0068 | 2 | HG01256.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.399+4713T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846613 | ||||||
| chr20:50846614
|
T | C | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.399+4714T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846614 | ||||||
| chr20:50846685
|
C | T | 1 | a0002c0002t0001g0067 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.399+4785C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846685 | ||||||
| chr20:50846688
|
A | G | 46 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(43): Show | 46 | HG00408.hp1 HG00423.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.399+4788A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846688 | ||||||
| chr20:50846697
|
T | C | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+4797T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846697 | ||||||
| chr20:50846717
|
G | A | 1 | a0002c0002t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.399+4817G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50846717 | ||||||
| chr20:50847055
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.399+5155G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847055 | ||||||
| chr20:50847062
|
C | T | 3 | a0001c0001t0002g0124a0001c0001t0002g0138a0001c0001t0004g0136 | 3 | HG00558.hp2 HG02523.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.399+5162C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847062 | ||||||
| chr20:50847189
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.399+5289C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847189 | ||||||
| chr20:50847231
|
C | T | 8 | a0001c0001t0002g0074a0001c0001t0002g0165a0001c0001t0002g0211others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.399+5331C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847231 | ||||||
| chr20:50847259
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.399+5359G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847259 | ||||||
| chr20:50847306
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.399+5406C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847306 | ||||||
| chr20:50847318
|
C | G | 3 | a0003c0005t0006g0082a0003c0005t0006g0084a0003c0005t0006g0085 | 3 | HG01361.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.399+5418C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847318 | ||||||
| chr20:50847338
|
C | T | 5 | a0001c0001t0003g0065a0001c0001t0003g0223a0001c0001t0003g0227others(2): Show | 5 | HG01261.hp1 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+5438C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847338 | ||||||
| chr20:50847382
|
C | T | 67 | a0001c0001t0001g0075a0001c0001t0001g0175a0001c0001t0001g0212others(64): Show | 67 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.399+5482C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847382 | ||||||
| chr20:50847459
|
G | A | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+5559G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847459 | ||||||
| chr20:50847658
|
T | A | 2 | a0002c0002t0001g0031a0002c0002t0001g0052 | 2 | HG02155.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.399+5758T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847658 | ||||||
| chr20:50847672
|
C | T | 11 | a0001c0001t0002g0074a0001c0001t0002g0165a0001c0001t0002g0211others(8): Show | 11 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.399+5772C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847672 | ||||||
| chr20:50847771
|
G | A | 5 | a0001c0001t0003g0002a0001c0001t0003g0242a0001c0001t0005g0200others(2): Show | 5 | HG00642.hp1 HG01884.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+5871G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847771 | ||||||
| chr20:50847799
|
T | C | 11 | a0001c0001t0002g0074a0001c0001t0002g0165a0001c0001t0002g0211others(8): Show | 11 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.399+5899T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847799 | ||||||
| chr20:50847884
|
A | T | 10 | a0001c0001t0002g0076a0001c0001t0002g0101a0001c0001t0002g0118others(7): Show | 10 | HG00621.hp2 HG01952.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.399+5984A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50847884 | ||||||
| chr20:50848057
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.399+6157C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50848057 | ||||||
| chr20:50848060
|
A | C | 42 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(39): Show | 42 | HG00408.hp1 HG00423.hp2 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.399+6160A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50848060 | ||||||
| chr20:50848061
|
A | G | 11 | a0001c0001t0002g0074a0001c0001t0002g0165a0001c0001t0002g0211others(8): Show | 11 | HG01361.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.399+6161A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50848061 | ||||||
| chr20:50848098
|
G | T | 1 | a0002c0002t0001g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.399+6198G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50848098 | ||||||
| chr20:50848388
|
G | A | 2 | a0001c0001t0001g0249a0002c0002t0001g0039 | 2 | HG01261.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.399+6488G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50848388 | ||||||
| chr20:50848416
|
G | A | 42 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(39): Show | 42 | HG00408.hp1 HG00423.hp2 HG01256.hp1 others(39): Show |
intron_variant | MODIFIER | c.399+6516G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50848416 | ||||||
| chr20:50848865
|
T | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(135): Show | 138 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.399+6965T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50848865 | ||||||
| chr20:50848950
|
G | A | 1 | a0002c0002t0003g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.399+7050G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50848950 | ||||||
| chr20:50848989
|
C | T | 9 | a0001c0001t0001g0144a0001c0001t0002g0105a0001c0001t0002g0106others(6): Show | 9 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.399+7089C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50848989 | ||||||
| chr20:50849097
|
A | G | 29 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0179others(26): Show | 29 | HG00408.hp1 HG01256.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.399+7197A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50849097 | ||||||
| chr20:50849258
|
G | A | 8 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(5): Show | 8 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+7358G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50849258 | ||||||
| chr20:50849317
|
G | A | 8 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0192others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+7417G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50849317 | ||||||
| chr20:50849318
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(137): Show | 140 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.399+7418A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50849318 | ||||||
| chr20:50849329
|
G | A | 1 | a0001c0001t0002g0213 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.399+7429G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50849329 | ||||||
| chr20:50849480
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+7580C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50849480 | ||||||
| chr20:50849731
|
A | G | 2 | a0001c0001t0002g0169a0002c0002t0001g0069 | 2 | NA18975.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.399+7831A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50849731 | ||||||
| chr20:50849756
|
G | T | 21 | a0001c0001t0001g0089a0001c0001t0001g0144a0001c0001t0001g0168others(18): Show | 21 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.399+7856G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50849756 | ||||||
| chr20:50850226
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.399+8326A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850226 | ||||||
| chr20:50850276
|
A | T | 9 | a0001c0001t0001g0144a0001c0001t0002g0105a0001c0001t0002g0106others(6): Show | 9 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.399+8376A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850276 | ||||||
| chr20:50850378
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.399+8478C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850378 | ||||||
| chr20:50850379
|
T | G | 1 | a0001c0001t0001g0267 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.399+8479T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850379 | ||||||
| chr20:50850620
|
G | GC | 29 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0179others(26): Show | 29 | HG00408.hp1 HG01256.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.399+8720_399+8721i others(3): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850620 | ||||||
| chr20:50850632
|
C | G | 29 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0179others(26): Show | 29 | HG00408.hp1 HG01256.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.399+8732C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850632 | ||||||
| chr20:50850749
|
G | A | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+8849G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850749 | ||||||
| chr20:50850792
|
C | A | 9 | a0001c0001t0002g0086a0001c0001t0002g0230a0001c0001t0002g0257others(6): Show | 9 | HG00741.hp1 HG01167.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+8892C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850792 | ||||||
| chr20:50850792
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.399+8892C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850792 | ||||||
| chr20:50850793
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.399+8893G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850793 | ||||||
| chr20:50850833
|
A | G | 30 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0179others(27): Show | 30 | HG00408.hp1 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.399+8933A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850833 | ||||||
| chr20:50850879
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0002c0002t0001g0047 | 3 | HG01256.hp2 HG01258.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.399+8979C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850879 | ||||||
| chr20:50850946
|
G | A | 9 | a0001c0001t0001g0144a0001c0001t0002g0105a0001c0001t0002g0106others(6): Show | 9 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.399+9046G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850946 | ||||||
| chr20:50850978
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.399+9078C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50850978 | ||||||
| chr20:50851005
|
C | A | 5 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(2): Show | 5 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+9105C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851005 | ||||||
| chr20:50851006
|
T | TC | 269 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0075others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.399+9110dupC | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50851006 | |||||
| chr20:50851013
|
C | T | 4 | a0001c0001t0001g0143a0001c0001t0001g0161a0001c0001t0001g0167others(1): Show | 4 | HG02027.hp1 HG02074.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.399+9113C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851013 | ||||||
| chr20:50851015
|
AC | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0075others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.399+9122delC | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50851015 | |||||
| chr20:50851073
|
TG | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0075others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.399+9179delG | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50851073 | |||||
| chr20:50851101
|
A | G | 3 | a0003c0005t0006g0082a0003c0005t0006g0084a0003c0005t0006g0085 | 3 | HG01361.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.399+9201A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851101 | ||||||
| chr20:50851128
|
AG | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0075others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.399+9231delG | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50851128 | |||||
| chr20:50851134
|
C | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0075others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.399+9234C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851134 | ||||||
| chr20:50851187
|
A | G | 2 | a0002c0002t0001g0024a0002c0002t0004g0260 | 2 | NA18974.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.399+9287A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851187 | ||||||
| chr20:50851312
|
G | A | 1 | a0002c0002t0001g0052 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.399+9412G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851312 | ||||||
| chr20:50851332
|
G | A | 1 | a0002c0002t0001g0060 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.399+9432G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851332 | ||||||
| chr20:50851372
|
C | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+9472C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851372 | ||||||
| chr20:50851510
|
A | G | 40 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0168others(37): Show | 40 | HG00408.hp1 HG00423.hp2 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.399+9610A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851510 | ||||||
| chr20:50851604
|
G | C | 17 | a0001c0001t0001g0144a0001c0001t0002g0074a0001c0001t0002g0105others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.399+9704G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851604 | ||||||
| chr20:50851622
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.399+9722A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851622 | ||||||
| chr20:50851631
|
T | G | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+9731T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851631 | ||||||
| chr20:50851694
|
C | G | 41 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(38): Show | 41 | HG00408.hp1 HG00423.hp2 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.399+9794C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851694 | ||||||
| chr20:50851967
|
C | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0140others(14): Show | 17 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.399+10067C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50851967 | ||||||
| chr20:50852030
|
T | G | 1 | a0001c0001t0002g0086 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.399+10130T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50852030 | ||||||
| chr20:50852132
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.399+10232G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50852132 | ||||||
| chr20:50852316
|
G | A | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.399+10416G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50852316 | ||||||
| chr20:50852366
|
T | TTG | 71 | a0001c0001t0001g0075a0001c0001t0001g0175a0001c0001t0001g0212others(68): Show | 71 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.399+10486_399+1048 others(6): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50852366 | |||||
| chr20:50852506
|
T | C | 127 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(124): Show | 127 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.399+10606T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50852506 | ||||||
| chr20:50852576
|
T | TTTGCCAT others(16): Show |
2 | a0001c0001t0001g0001a0001c0001t0006g0077 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.399+10680_399+1070 others(27): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50852576 | |||||
| chr20:50852624
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.399+10724C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50852624 | ||||||
| chr20:50852625
|
G | T | 9 | a0001c0001t0001g0144a0001c0001t0002g0105a0001c0001t0002g0106others(6): Show | 9 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.399+10725G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50852625 | ||||||
| chr20:50852671
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(145): Show | 148 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.399+10771T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50852671 | ||||||
| chr20:50852677
|
C | T | 44 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(41): Show | 44 | HG00408.hp1 HG00423.hp2 HG01256.hp1 others(41): Show |
intron_variant | MODIFIER | c.399+10777C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50852677 | ||||||
| chr20:50852716
|
T | C | 3 | a0001c0001t0002g0127a0001c0001t0002g0229a0001c0001t0002g0231 | 3 | NA18950.hp1 NA18966.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.399+10816T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50852716 | ||||||
| chr20:50852834
|
A | G | 1 | a0002c0002t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.399+10934A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50852834 | ||||||
| chr20:50852916
|
G | A | 50 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(47): Show | 50 | HG00408.hp1 HG00423.hp2 HG01256.hp1 others(47): Show |
intron_variant | MODIFIER | c.399+11016G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50852916 | ||||||
| chr20:50853079
|
A | G | 1 | a0006c0009t0001g0010 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.399+11179A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853079 | ||||||
| chr20:50853139
|
A | AT | 12 | a0001c0001t0001g0075a0001c0001t0001g0102a0001c0001t0002g0138others(9): Show | 12 | HG01106.hp2 HG01261.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+11262dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853139 | |||||
| chr20:50853139
|
AT | A | 13 | a0001c0001t0001g0001a0001c0001t0002g0118a0001c0001t0002g0141others(10): Show | 13 | HG01074.hp1 HG01433.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.399+11262delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853139 | |||||
| chr20:50853139
|
ATT | A | 51 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(48): Show | 51 | HG00408.hp1 HG00423.hp2 HG01256.hp1 others(48): Show |
intron_variant | MODIFIER | c.399+11261_399+1126 others(6): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853139 | |||||
| chr20:50853139
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0005g0221 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.399+11250_399+1126 others(17): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853139 | |||||
| chr20:50853365
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0006g0077 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.399+11465G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853365 | ||||||
| chr20:50853506
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.399+11606G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853506 | ||||||
| chr20:50853515
|
C | T | 1 | a0003c0005t0002g0128 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.399+11615C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853515 | ||||||
| chr20:50853605
|
A | T | 12 | a0001c0001t0001g0238a0001c0001t0003g0209a0001c0001t0003g0210others(9): Show | 12 | HG01943.hp2 HG01978.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+11705A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853605 | ||||||
| chr20:50853617
|
A | C | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.399+11717A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853617 | ||||||
| chr20:50853683
|
G | GGGGTGTT others(180): Show |
20 | a0001c0001t0001g0088a0001c0001t0001g0120a0001c0001t0001g0131others(17): Show | 20 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.399+11795_399+1179 others(191): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853683 | |||||
| chr20:50853683
|
G | GGGGTGTT others(161): Show |
102 | a0001c0001t0001g0022a0001c0001t0001g0087a0001c0001t0001g0091others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.399+11795_399+1179 others(172): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853683 | |||||
| chr20:50853686
|
G | GTGTTTTG others(68): Show |
102 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(99): Show | 102 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.399+11795_399+1179 others(79): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853686 | |||||
| chr20:50853696
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0140others(42): Show | 45 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.399+11796T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853696 | ||||||
| chr20:50853701
|
G | GGGGGTGT others(143): Show |
25 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0140others(22): Show | 25 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.399+11804_399+1180 others(154): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853701 | |||||
| chr20:50853701
|
G | GGGGGTGT others(124): Show |
2 | a0002c0002t0003g0035a0002c0002t0003g0036 | 2 | HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.399+11804_399+1180 others(135): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853701 | |||||
| chr20:50853704
|
G | GGTGTTTT others(50): Show |
18 | a0001c0001t0001g0188a0001c0001t0001g0238a0001c0001t0002g0086others(15): Show | 18 | HG00741.hp1 HG01167.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.399+11804_399+1180 others(61): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853704 | ||||||
| chr20:50853717
|
TG | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0140others(42): Show | 45 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.399+11823delG | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853717 | |||||
| chr20:50853723
|
G | A | 2 | a0001c0001t0002g0169a0002c0002t0001g0069 | 2 | NA18975.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.399+11823G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853723 | ||||||
| chr20:50853755
|
T | TG | 17 | a0001c0001t0002g0074a0001c0001t0002g0086a0001c0001t0002g0124others(14): Show | 17 | HG00741.hp1 HG01167.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.399+11860dupG | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853755 | |||||
| chr20:50853775
|
GA | G | 9 | a0001c0001t0002g0086a0001c0001t0002g0230a0001c0001t0002g0257others(6): Show | 9 | HG00741.hp1 HG01167.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+11876delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853775 | ||||||
| chr20:50853794
|
G | GA | 9 | a0001c0001t0002g0086a0001c0001t0002g0230a0001c0001t0002g0257others(6): Show | 9 | HG00741.hp1 HG01167.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+11894_399+1189 others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853794 | ||||||
| chr20:50853794
|
G | GGGGTGTT others(49): Show |
1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.399+11896_399+1189 others(60): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853794 | |||||
| chr20:50853797
|
A | G | 119 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(116): Show | 119 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.399+11897A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853797 | ||||||
| chr20:50853797
|
A | GTGTTTTG others(11): Show |
1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.399+11879_399+1189 others(22): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853797 | ||||||
| chr20:50853813
|
GA | G | 9 | a0001c0001t0002g0086a0001c0001t0002g0230a0001c0001t0002g0257others(6): Show | 9 | HG00741.hp1 HG01167.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+11914delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853813 | ||||||
| chr20:50853814
|
A | G | 61 | a0001c0001t0001g0075a0001c0001t0001g0175a0001c0001t0001g0212others(58): Show | 61 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.399+11914A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853814 | ||||||
| chr20:50853845
|
C | T | 69 | a0001c0001t0001g0075a0001c0001t0001g0175a0001c0001t0001g0212others(66): Show | 69 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.399+11945C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853845 | ||||||
| chr20:50853848
|
T | TG | 9 | a0001c0001t0002g0086a0001c0001t0002g0230a0001c0001t0002g0257others(6): Show | 9 | HG00741.hp1 HG01167.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+11949dupG | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853848 | |||||
| chr20:50853850
|
T | G | 69 | a0001c0001t0001g0075a0001c0001t0001g0175a0001c0001t0001g0212others(66): Show | 69 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.399+11950T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853850 | ||||||
| chr20:50853851
|
A | AG | 60 | a0001c0001t0001g0075a0001c0001t0001g0175a0001c0001t0001g0212others(57): Show | 60 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.399+11952dupG | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50853851 | |||||
| chr20:50853851
|
A | G | 9 | a0001c0001t0002g0086a0001c0001t0002g0230a0001c0001t0002g0257others(6): Show | 9 | HG00741.hp1 HG01167.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.399+11951A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853851 | ||||||
| chr20:50853853
|
A | G | 69 | a0001c0001t0001g0075a0001c0001t0001g0175a0001c0001t0001g0212others(66): Show | 69 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.399+11953A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853853 | ||||||
| chr20:50853862
|
A | G | 69 | a0001c0001t0001g0075a0001c0001t0001g0175a0001c0001t0001g0212others(66): Show | 69 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.399+11962A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50853862 | ||||||
| chr20:50854138
|
A | C | 14 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(11): Show | 14 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.399+12238A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854138 | ||||||
| chr20:50854281
|
G | A | 21 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0140others(18): Show | 21 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.399+12381G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854281 | ||||||
| chr20:50854311
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0006g0077 | 2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.399+12411G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854311 | ||||||
| chr20:50854345
|
G | A | 8 | a0001c0001t0002g0074a0001c0001t0002g0165a0001c0001t0002g0211others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.399+12445G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854345 | ||||||
| chr20:50854442
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.399+12542C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854442 | ||||||
| chr20:50854516
|
C | T | 8 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0192others(5): Show | 8 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+12616C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854516 | ||||||
| chr20:50854775
|
G | A | 1 | a0002c0002t0002g0032 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.399+12875G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854775 | ||||||
| chr20:50854825
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.399+12925T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854825 | ||||||
| chr20:50854835
|
T | G | 127 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(124): Show | 127 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.399+12935T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854835 | ||||||
| chr20:50854888
|
A | G | 119 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(116): Show | 119 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.399+12988A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854888 | ||||||
| chr20:50854927
|
C | T | 7 | a0001c0001t0001g0238a0001c0001t0003g0209a0001c0001t0003g0210others(4): Show | 7 | HG01943.hp2 HG01978.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.399+13027C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854927 | ||||||
| chr20:50854985
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.399+13085C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50854985 | ||||||
| chr20:50855006
|
G | A | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.399+13106G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50855006 | ||||||
| chr20:50855036
|
G | A | 8 | a0001c0001t0002g0074a0001c0001t0002g0165a0001c0001t0002g0211others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.399+13136G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50855036 | ||||||
| chr20:50855248
|
G | C | 1 | a0001c0001t0001g0144 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.399+13348G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50855248 | ||||||
| chr20:50855398
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.399+13498G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50855398 | ||||||
| chr20:50855470
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.399+13570C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50855470 | ||||||
| chr20:50855497
|
C | T | 1 | a0002c0002t0001g0056 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.399+13597C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50855497 | ||||||
| chr20:50855576
|
T | TGGAAGG | 8 | a0001c0001t0002g0074a0001c0001t0002g0165a0001c0001t0002g0211others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.399+13690_399+1369 others(10): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50855576 | |||||
| chr20:50855611
|
C | A | 80 | a0001c0001t0001g0075a0001c0001t0001g0144a0001c0001t0001g0161others(77): Show | 80 | HG00558.hp2 HG00639.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.399+13711C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50855611 | ||||||
| chr20:50855784
|
C | T | 7 | a0001c0001t0001g0238a0001c0001t0003g0209a0001c0001t0003g0210others(4): Show | 7 | HG01943.hp2 HG01978.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.399+13884C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50855784 | ||||||
| chr20:50855802
|
C | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+13902C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50855802 | ||||||
| chr20:50855861
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.399+13961G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50855861 | ||||||
| chr20:50856008
|
G | A | 8 | a0001c0003t0001g0004a0001c0003t0001g0005a0001c0003t0001g0081others(5): Show | 8 | HG01243.hp2 HG01358.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+14108G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50856008 | ||||||
| chr20:50856132
|
C | T | 1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.399+14232C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50856132 | ||||||
| chr20:50856205
|
C | T | 50 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(47): Show | 50 | HG00408.hp1 HG00423.hp2 HG01256.hp1 others(47): Show |
intron_variant | MODIFIER | c.399+14305C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50856205 | ||||||
| chr20:50856249
|
G | A | 5 | a0001c0001t0003g0065a0001c0001t0003g0223a0001c0001t0003g0227others(2): Show | 5 | HG01261.hp1 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+14349G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50856249 | ||||||
| chr20:50857149
|
G | A | 14 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(11): Show | 14 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.399+15249G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50857149 | ||||||
| chr20:50857149
|
G | T | 106 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(103): Show | 106 | HG00408.hp1 HG00558.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.399+15249G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50857149 | ||||||
| chr20:50857179
|
C | T | 119 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(116): Show | 119 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.399+15279C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50857179 | ||||||
| chr20:50857358
|
G | A | 1 | a0001c0003t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.399+15458G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50857358 | ||||||
| chr20:50857567
|
G | A | 127 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(124): Show | 127 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.399+15667G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50857567 | ||||||
| chr20:50857574
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0006g0077a0003c0005t0006g0082others(2): Show | 5 | HG01361.hp2 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+15674G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50857574 | ||||||
| chr20:50857697
|
C | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(111): Show | 114 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.399+15797C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50857697 | ||||||
| chr20:50857824
|
C | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(85): Show | 88 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.399+15924C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50857824 | ||||||
| chr20:50858029
|
G | T | 7 | a0001c0001t0002g0074a0001c0001t0002g0165a0001c0001t0002g0211others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+16129G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858029 | ||||||
| chr20:50858054
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(188): Show | 191 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.399+16154A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858054 | ||||||
| chr20:50858267
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.399+16367A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858267 | ||||||
| chr20:50858356
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0002g0189 | 2 | HG00639.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.399+16456C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858356 | ||||||
| chr20:50858359
|
T | G | 1 | a0001c0001t0003g0242 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.399+16459T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858359 | ||||||
| chr20:50858445
|
T | C | 92 | a0001c0001t0001g0075a0001c0001t0001g0107a0001c0001t0001g0110others(89): Show | 92 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.399+16545T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858445 | ||||||
| chr20:50858453
|
T | C | 1 | a0001c0001t0002g0186 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.399+16553T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858453 | ||||||
| chr20:50858458
|
C | T | 25 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0002g0122others(22): Show | 25 | HG01106.hp2 HG01256.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.399+16558C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858458 | ||||||
| chr20:50858519
|
T | A | 1 | a0002c0002t0001g0025 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.399+16619T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858519 | ||||||
| chr20:50858556
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.399+16656C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858556 | ||||||
| chr20:50858558
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.399+16658C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858558 | ||||||
| chr20:50858571
|
C | T | 7 | a0001c0001t0002g0074a0001c0001t0002g0165a0001c0001t0002g0211others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+16671C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858571 | ||||||
| chr20:50858580
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.399+16680T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858580 | ||||||
| chr20:50858707
|
CT | C | 143 | a0001c0001t0001g0075a0001c0001t0001g0079a0001c0001t0001g0080others(140): Show | 143 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.399+16819delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50858707 | |||||
| chr20:50858725
|
A | AT | 8 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0179others(5): Show | 8 | HG00738.hp2 HG01978.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.399+16844dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50858725 | |||||
| chr20:50858725
|
A | ATT | 77 | a0001c0001t0001g0075a0001c0001t0001g0175a0001c0001t0001g0212others(74): Show | 77 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.399+16843_399+1684 others(6): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50858725 | |||||
| chr20:50858725
|
A | ATTT | 14 | a0001c0001t0001g0093a0001c0001t0001g0107a0001c0001t0001g0110others(11): Show | 14 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.399+16842_399+1684 others(7): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50858725 | |||||
| chr20:50858725
|
AT | A | 47 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(44): Show | 47 | HG00423.hp2 HG01099.hp1 HG01256.hp1 others(44): Show |
intron_variant | MODIFIER | c.399+16844delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50858725 | |||||
| chr20:50858758
|
C | T | 2 | a0001c0001t0002g0270a0001c0003t0001g0133 | 2 | HG02622.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.399+16858C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858758 | ||||||
| chr20:50858764
|
C | T | 2 | a0002c0002t0002g0068a0002c0002t0002g0070 | 2 | HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.399+16864C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858764 | ||||||
| chr20:50858774
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.399+16874G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858774 | ||||||
| chr20:50858777
|
A | G | 94 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0107others(91): Show | 94 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.399+16877A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858777 | ||||||
| chr20:50858825
|
C | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+16925C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858825 | ||||||
| chr20:50858861
|
G | C | 2 | a0002c0002t0002g0062a0002c0002t0002g0064 | 2 | HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.399+16961G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858861 | ||||||
| chr20:50858883
|
C | T | 2 | a0001c0001t0004g0235a0001c0004t0004g0007 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.399+16983C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858883 | ||||||
| chr20:50858925
|
C | CTAT | 75 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0093others(72): Show | 75 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.399+17045_399+1704 others(7): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50858925 | |||||
| chr20:50858925
|
C | CTATTAT | 49 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(46): Show | 49 | HG00423.hp2 HG01106.hp2 HG01256.hp1 others(46): Show |
intron_variant | MODIFIER | c.399+17042_399+1704 others(10): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50858925 | |||||
| chr20:50858939
|
A | ATTG | 24 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(21): Show | 24 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.399+17041_399+1704 others(7): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50858939 | |||||
| chr20:50858977
|
A | C | 60 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0110others(57): Show | 60 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.399+17077A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858977 | ||||||
| chr20:50858978
|
G | C | 60 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0110others(57): Show | 60 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.399+17078G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50858978 | ||||||
| chr20:50859036
|
C | G | 46 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(43): Show | 46 | HG00423.hp2 HG01106.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.399+17136C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859036 | ||||||
| chr20:50859188
|
C | T | 1 | a0001c0003t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.399+17288C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859188 | ||||||
| chr20:50859211
|
A | G | 93 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0107others(90): Show | 93 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.400-17275A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859211 | ||||||
| chr20:50859311
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.400-17175G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859311 | ||||||
| chr20:50859407
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.400-17079G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859407 | ||||||
| chr20:50859425
|
C | T | 1 | a0001c0003t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.400-17061C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859425 | ||||||
| chr20:50859549
|
A | AAGAGGGC others(21): Show |
51 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(48): Show | 51 | HG00423.hp2 HG01106.hp2 HG01256.hp1 others(48): Show |
intron_variant | MODIFIER | c.400-16935_400-1693 others(32): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50859549 | |||||
| chr20:50859605
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(145): Show | 148 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.400-16881C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859605 | ||||||
| chr20:50859641
|
G | A | 1 | a0001c0001t0002g0164 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.400-16845G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859641 | ||||||
| chr20:50859695
|
C | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.400-16791C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859695 | ||||||
| chr20:50859696
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0006g0077others(3): Show | 6 | HG01361.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-16790G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859696 | ||||||
| chr20:50859751
|
A | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(146): Show | 149 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.400-16735A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859751 | ||||||
| chr20:50859789
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.400-16697C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859789 | ||||||
| chr20:50859790
|
G | A | 26 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0179others(23): Show | 26 | HG01106.hp2 HG01256.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.400-16696G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859790 | ||||||
| chr20:50859861
|
C | T | 7 | a0001c0001t0001g0107a0001c0001t0001g0140a0001c0001t0001g0198others(4): Show | 7 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.400-16625C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859861 | ||||||
| chr20:50859891
|
A | G | 101 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0107others(98): Show | 101 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.400-16595A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859891 | ||||||
| chr20:50859979
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(145): Show | 148 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.400-16507G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50859979 | ||||||
| chr20:50860092
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.400-16394C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860092 | ||||||
| chr20:50860176
|
C | G | 6 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0006g0077others(3): Show | 6 | HG01361.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-16310C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860176 | ||||||
| chr20:50860272
|
C | T | 9 | a0001c0001t0001g0144a0001c0001t0002g0105a0001c0001t0002g0106others(6): Show | 9 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-16214C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860272 | ||||||
| chr20:50860297
|
A | G | 3 | a0001c0001t0002g0226a0001c0001t0002g0270a0001c0003t0001g0133 | 3 | HG02622.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.400-16189A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860297 | ||||||
| chr20:50860353
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.400-16133C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860353 | ||||||
| chr20:50860427
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(146): Show | 149 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.400-16059G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860427 | ||||||
| chr20:50860612
|
A | C | 1 | a0001c0001t0001g0267 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.400-15874A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860612 | ||||||
| chr20:50860618
|
A | G | 43 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(40): Show | 43 | HG00408.hp1 HG00423.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.400-15868A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860618 | ||||||
| chr20:50860662
|
G | T | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400-15824G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860662 | ||||||
| chr20:50860726
|
A | T | 1 | a0002c0002t0001g0031 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.400-15760A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860726 | ||||||
| chr20:50860730
|
G | A | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.400-15756G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860730 | ||||||
| chr20:50860856
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(148): Show | 151 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.400-15630T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860856 | ||||||
| chr20:50860893
|
A | G | 1 | a0001c0001t0005g0207 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.400-15593A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860893 | ||||||
| chr20:50860967
|
C | G | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400-15519C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860967 | ||||||
| chr20:50860995
|
T | C | 2 | a0002c0002t0002g0068a0002c0002t0002g0070 | 2 | HG01256.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.400-15491T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50860995 | ||||||
| chr20:50860997
|
GA | G | 27 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0179others(24): Show | 27 | HG00408.hp1 HG01106.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.400-15473delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50860997 | |||||
| chr20:50861212
|
T | C | 1 | a0001c0003t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.400-15274T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50861212 | ||||||
| chr20:50861283
|
C | T | 1 | a0001c0004t0002g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.400-15203C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50861283 | ||||||
| chr20:50861292
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.400-15194C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50861292 | ||||||
| chr20:50861321
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.400-15165C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50861321 | ||||||
| chr20:50861330
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(148): Show | 151 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.400-15156A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50861330 | ||||||
| chr20:50861335
|
C | G | 1 | a0002c0002t0001g0083 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.400-15151C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50861335 | ||||||
| chr20:50861341
|
G | A | 4 | a0001c0001t0002g0119a0001c0001t0002g0124a0001c0001t0002g0138others(1): Show | 4 | HG00558.hp2 HG02523.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-15145G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50861341 | ||||||
| chr20:50861353
|
G | A | 4 | a0001c0001t0003g0239a0001c0001t0003g0240a0001c0001t0003g0241others(1): Show | 4 | HG02055.hp1 HG03139.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-15133G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50861353 | ||||||
| chr20:50861463
|
G | A | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.400-15023G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50861463 | ||||||
| chr20:50861697
|
C | G | 12 | a0001c0001t0001g0089a0001c0001t0001g0168a0001c0001t0003g0219others(9): Show | 12 | HG00423.hp2 HG01256.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.400-14789C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50861697 | ||||||
| chr20:50861846
|
C | CT | 18 | a0001c0001t0002g0141a0001c0001t0002g0162a0001c0001t0002g0164others(15): Show | 18 | HG00609.hp2 HG01074.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.400-14616dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50861846 | |||||
| chr20:50861846
|
CT | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(38): Show | 41 | HG00423.hp2 HG01106.hp2 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.400-14616delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50861846 | |||||
| chr20:50861846
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0144 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.400-14629_400-1461 others(18): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50861846 | |||||
| chr20:50862148
|
C | T | 101 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0107others(98): Show | 101 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.400-14338C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50862148 | ||||||
| chr20:50862223
|
C | G | 99 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0107others(96): Show | 99 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.400-14263C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50862223 | ||||||
| chr20:50862563
|
A | ACCTC | 61 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0110others(58): Show | 61 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.400-13921_400-1391 others(8): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50862563 | |||||
| chr20:50862640
|
G | A | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400-13846G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50862640 | ||||||
| chr20:50862689
|
T | G | 1 | a0001c0001t0003g0236 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.400-13797T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50862689 | ||||||
| chr20:50862778
|
G | A | 2 | a0002c0002t0002g0062a0002c0002t0002g0064 | 2 | HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.400-13708G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50862778 | ||||||
| chr20:50862947
|
C | T | 13 | a0001c0001t0002g0119a0001c0001t0002g0124a0001c0001t0002g0138others(10): Show | 13 | HG00558.hp2 HG01261.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-13539C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50862947 | ||||||
| chr20:50863226
|
T | C | 43 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(40): Show | 43 | HG00408.hp1 HG00423.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.400-13260T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50863226 | ||||||
| chr20:50863239
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.400-13247T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50863239 | ||||||
| chr20:50863244
|
GGTGCTTT others(42): Show |
G | 1 | a0001c0001t0001g0022 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.400-13239_400-1319 others(53): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50863244 | |||||
| chr20:50863248
|
C | CT | 55 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0102others(52): Show | 55 | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.400-13211dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50863248 | |||||
| chr20:50863248
|
C | CTT | 15 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0140others(12): Show | 15 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.400-13212_400-1321 others(6): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50863248 | |||||
| chr20:50863248
|
C | CTTTTT | 6 | a0001c0001t0002g0106a0001c0001t0002g0192a0001c0001t0002g0213others(3): Show | 6 | HG02895.hp1 HG02922.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-13215_400-1321 others(9): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50863248 | |||||
| chr20:50863248
|
CT | C | 7 | a0001c0001t0001g0125a0001c0001t0001g0144a0001c0001t0001g0168others(4): Show | 7 | HG01099.hp2 HG01106.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-13211delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50863248 | |||||
| chr20:50863404
|
C | T | 2 | a0001c0001t0003g0002a0001c0001t0003g0242 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.400-13082C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50863404 | ||||||
| chr20:50863426
|
T | G | 2 | a0001c0001t0002g0101a0001c0001t0002g0191 | 2 | HG00621.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.400-13060T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50863426 | ||||||
| chr20:50863501
|
G | A | 1 | a0002c0002t0004g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.400-12985G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50863501 | ||||||
| chr20:50863762
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0107others(45): Show | 48 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.400-12724G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50863762 | ||||||
| chr20:50863814
|
G | A | 28 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0179others(25): Show | 28 | HG01256.hp2 HG01258.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.400-12672G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50863814 | ||||||
| chr20:50863842
|
C | G | 9 | a0001c0001t0002g0086a0001c0001t0002g0230a0001c0001t0002g0257others(6): Show | 9 | HG00741.hp1 HG01167.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-12644C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50863842 | ||||||
| chr20:50863892
|
GCTCTGTC others(4): Show |
G | 80 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(77): Show | 80 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.400-12593_400-1258 others(15): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50863892 | ||||||
| chr20:50863902
|
G | T | 56 | a0001c0001t0001g0075a0001c0001t0001g0093a0001c0001t0001g0110others(53): Show | 56 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.400-12584G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50863902 | ||||||
| chr20:50864014
|
C | T | 2 | a0002c0002t0001g0019a0002c0002t0004g0061 | 2 | NA18971.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.400-12472C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50864014 | ||||||
| chr20:50864063
|
G | C | 30 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0093others(27): Show | 30 | HG01256.hp2 HG01258.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.400-12423G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50864063 | ||||||
| chr20:50864221
|
C | G | 1 | a0001c0008t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.400-12265C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50864221 | ||||||
| chr20:50864267
|
G | C | 1 | a0001c0001t0003g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.400-12219G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50864267 | ||||||
| chr20:50864438
|
GA | G | 66 | a0001c0001t0001g0075a0001c0001t0001g0107a0001c0001t0001g0140others(63): Show | 66 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.400-12047delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50864438 | ||||||
| chr20:50864438
|
GAT | G | 26 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0093others(23): Show | 26 | HG01256.hp2 HG01258.hp2 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.400-12047_400-1204 others(6): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50864438 | ||||||
| chr20:50864439
|
A | T | 9 | a0001c0001t0001g0001a0001c0001t0002g0017a0001c0001t0002g0226others(6): Show | 9 | HG01361.hp2 HG01952.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-12047A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50864439 | ||||||
| chr20:50864439
|
AT | A | 50 | a0001c0001t0001g0100a0001c0001t0001g0110a0001c0001t0001g0149others(47): Show | 50 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.400-12028delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50864439 | |||||
| chr20:50864624
|
G | A | 41 | a0001c0001t0001g0001a0001c0001t0001g0107a0001c0001t0001g0140others(38): Show | 41 | HG00423.hp1 HG00621.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.400-11862G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50864624 | ||||||
| chr20:50864717
|
G | T | 2 | a0001c0004t0001g0012a0002c0002t0003g0057 | 2 | HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.400-11769G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50864717 | ||||||
| chr20:50864774
|
G | A | 1 | a0001c0001t0003g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.400-11712G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50864774 | ||||||
| chr20:50864899
|
G | A | 8 | a0001c0001t0002g0074a0001c0001t0002g0165a0001c0001t0002g0211others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-11587G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50864899 | ||||||
| chr20:50865072
|
G | A | 43 | a0001c0001t0001g0110a0001c0001t0002g0119a0001c0001t0002g0129others(40): Show | 43 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.400-11414G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50865072 | ||||||
| chr20:50865072
|
G | T | 1 | a0002c0002t0003g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.400-11414G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50865072 | ||||||
| chr20:50865125
|
C | T | 1 | a0002c0002t0001g0060 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.400-11361C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50865125 | ||||||
| chr20:50865190
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.400-11296G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50865190 | ||||||
| chr20:50865422
|
G | T | 26 | a0001c0001t0001g0075a0001c0001t0001g0179a0001c0001t0001g0212others(23): Show | 26 | HG00741.hp1 HG01106.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.400-11064G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50865422 | ||||||
| chr20:50865451
|
G | T | 1 | a0001c0003t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.400-11035G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50865451 | ||||||
| chr20:50865548
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.400-10938A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50865548 | ||||||
| chr20:50865559
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.400-10927C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50865559 | ||||||
| chr20:50865713
|
GGGCCGGC others(3): Show |
G | 1 | a0001c0003t0001g0094 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.400-10769_400-1076 others(14): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50865713 | |||||
| chr20:50866005
|
A | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(135): Show | 138 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.400-10481A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866005 | ||||||
| chr20:50866007
|
C | T | 42 | a0001c0001t0001g0110a0001c0001t0002g0119a0001c0001t0002g0129others(39): Show | 42 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.400-10479C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866007 | ||||||
| chr20:50866097
|
G | C | 1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.400-10389G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866097 | ||||||
| chr20:50866129
|
G | A | 1 | a0001c0001t0002g0158 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.400-10357G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866129 | ||||||
| chr20:50866219
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400-10267C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866219 | ||||||
| chr20:50866223
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.400-10263G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866223 | ||||||
| chr20:50866331
|
G | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0110others(73): Show | 76 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.400-10155G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866331 | ||||||
| chr20:50866364
|
C | G | 1 | a0002c0002t0003g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.400-10122C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866364 | ||||||
| chr20:50866396
|
G | A | 42 | a0001c0001t0001g0110a0001c0001t0002g0119a0001c0001t0002g0129others(39): Show | 42 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.400-10090G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866396 | ||||||
| chr20:50866481
|
A | G | 2 | a0002c0002t0001g0023a0002c0002t0001g0044 | 2 | HG02056.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.400-10005A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866481 | ||||||
| chr20:50866558
|
C | G | 27 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0093others(24): Show | 27 | HG01256.hp2 HG01258.hp2 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.400-9928C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866558 | ||||||
| chr20:50866872
|
G | A | 1 | a0001c0001t0002g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.400-9614G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50866872 | ||||||
| chr20:50867245
|
A | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0002g0226others(4): Show | 7 | HG01361.hp2 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-9241A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50867245 | ||||||
| chr20:50867293
|
C | T | 42 | a0001c0001t0001g0110a0001c0001t0002g0119a0001c0001t0002g0129others(39): Show | 42 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.400-9193C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50867293 | ||||||
| chr20:50867340
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.400-9146G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50867340 | ||||||
| chr20:50867377
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0238a0002c0002t0001g0048 | 3 | HG01123.hp1 HG01981.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.400-9109C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50867377 | ||||||
| chr20:50867390
|
A | T | 2 | a0001c0001t0002g0017a0001c0001t0002g0162 | 2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.400-9096A>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50867390 | ||||||
| chr20:50867545
|
A | G | 1 | a0005c0007t0002g0150 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.400-8941A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50867545 | ||||||
| chr20:50867866
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.400-8620A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50867866 | ||||||
| chr20:50867908
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.400-8578C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50867908 | ||||||
| chr20:50868082
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.400-8404A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868082 | ||||||
| chr20:50868261
|
C | T | 2 | a0001c0001t0001g0123a0002c0002t0001g0028 | 2 | NA18950.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.400-8225C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868261 | ||||||
| chr20:50868324
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.400-8162C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868324 | ||||||
| chr20:50868350
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.400-8136G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868350 | ||||||
| chr20:50868407
|
A | G | 1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.400-8079A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868407 | ||||||
| chr20:50868525
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0144a0001c0001t0006g0077others(3): Show | 6 | HG01361.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-7961C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868525 | ||||||
| chr20:50868625
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.400-7861A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868625 | ||||||
| chr20:50868682
|
C | T | 1 | a0001c0001t0002g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.400-7804C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868682 | ||||||
| chr20:50868730
|
C | T | 7 | a0001c0001t0002g0074a0001c0001t0002g0165a0001c0001t0002g0211others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-7756C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868730 | ||||||
| chr20:50868930
|
G | T | 3 | a0001c0001t0003g0227a0002c0002t0003g0035a0002c0002t0003g0036 | 3 | HG02258.hp2 HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.400-7556G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868930 | ||||||
| chr20:50868931
|
C | T | 4 | a0001c0001t0001g0093a0001c0001t0002g0169a0002c0002t0001g0025others(1): Show | 4 | NA18975.hp2 NA19007.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-7555C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868931 | ||||||
| chr20:50868932
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.400-7554G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868932 | ||||||
| chr20:50868975
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(142): Show | 145 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.400-7511A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50868975 | ||||||
| chr20:50869179
|
T | G | 1 | a0001c0001t0002g0270 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.400-7307T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50869179 | ||||||
| chr20:50869409
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(99): Show | 102 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.400-7077A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50869409 | ||||||
| chr20:50869430
|
C | G | 1 | a0001c0004t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.400-7056C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50869430 | ||||||
| chr20:50869742
|
C | CT | 24 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0117others(21): Show | 24 | HG00408.hp2 HG01358.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.400-6720dupT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50869742 | |||||
| chr20:50869742
|
C | CTT | 36 | a0001c0001t0001g0110a0001c0001t0002g0129a0001c0001t0002g0135others(33): Show | 36 | HG00099.hp1 HG00558.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.400-6721_400-6720d others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50869742 | |||||
| chr20:50869742
|
C | CTTT | 6 | a0001c0001t0002g0174a0001c0001t0003g0239a0001c0001t0003g0241others(3): Show | 6 | HG00423.hp2 HG01433.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-6722_400-6720d others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50869742 | |||||
| chr20:50869742
|
CT | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(85): Show | 88 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.400-6720delT | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50869742 | |||||
| chr20:50869873
|
C | T | 25 | a0001c0001t0001g0075a0001c0001t0001g0179a0001c0001t0001g0212others(22): Show | 25 | HG00741.hp1 HG01106.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.400-6613C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50869873 | ||||||
| chr20:50869874
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(91): Show | 94 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(91): Show |
intron_variant | MODIFIER | c.400-6612A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50869874 | ||||||
| chr20:50870009
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0079others(89): Show | 92 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(89): Show |
intron_variant | MODIFIER | c.400-6477G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50870009 | ||||||
| chr20:50870537
|
T | G | 37 | a0001c0001t0001g0001a0001c0001t0002g0074a0001c0001t0002g0086others(34): Show | 37 | HG00741.hp1 HG01167.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.400-5949T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50870537 | ||||||
| chr20:50870871
|
G | A | 2 | a0001c0001t0007g0262a0001c0001t0007g0265 | 2 | HG01071.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.400-5615G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50870871 | ||||||
| chr20:50870964
|
G | C | 2 | a0001c0001t0002g0215a0001c0001t0006g0077 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.400-5522G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50870964 | ||||||
| chr20:50870978
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0008g0258 | 2 | HG01070.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.400-5508C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50870978 | ||||||
| chr20:50871164
|
C | T | 3 | a0003c0005t0006g0082a0003c0005t0006g0084a0003c0005t0006g0085 | 3 | HG01361.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.400-5322C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871164 | ||||||
| chr20:50871195
|
G | C | 4 | a0001c0003t0001g0133a0003c0005t0006g0082a0003c0005t0006g0084others(1): Show | 4 | HG01361.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-5291G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871195 | ||||||
| chr20:50871244
|
G | A | 110 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0087others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.400-5242G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871244 | ||||||
| chr20:50871270
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.400-5216C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871270 | ||||||
| chr20:50871291
|
G | A | 1 | a0001c0001t0002g0164 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.400-5195G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871291 | ||||||
| chr20:50871307
|
G | A | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400-5179G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871307 | ||||||
| chr20:50871312
|
A | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0075a0001c0001t0001g0179others(138): Show | 141 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.400-5174A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871312 | ||||||
| chr20:50871364
|
A | G | 4 | a0001c0003t0001g0133a0003c0005t0006g0082a0003c0005t0006g0084others(1): Show | 4 | HG01361.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-5122A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871364 | ||||||
| chr20:50871365
|
A | C | 4 | a0001c0003t0001g0133a0003c0005t0006g0082a0003c0005t0006g0084others(1): Show | 4 | HG01361.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-5121A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871365 | ||||||
| chr20:50871366
|
A | G | 4 | a0001c0003t0001g0133a0003c0005t0006g0082a0003c0005t0006g0084others(1): Show | 4 | HG01361.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-5120A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871366 | ||||||
| chr20:50871410
|
G | A | 6 | a0001c0003t0001g0004a0001c0003t0001g0005a0001c0003t0001g0096others(3): Show | 6 | HG02280.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-5076G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871410 | ||||||
| chr20:50871452
|
C | T | 1 | a0002c0002t0003g0054 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.400-5034C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871452 | ||||||
| chr20:50871455
|
C | T | 8 | a0001c0003t0001g0004a0001c0003t0001g0005a0001c0003t0001g0081others(5): Show | 8 | HG01243.hp2 HG01358.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.400-5031C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871455 | ||||||
| chr20:50871606
|
G | A | 20 | a0001c0001t0002g0121a0001c0001t0002g0129a0001c0001t0002g0135others(17): Show | 20 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.400-4880G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871606 | ||||||
| chr20:50871674
|
C | T | 1 | a0001c0001t0002g0141 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.400-4812C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871674 | ||||||
| chr20:50871677
|
G | A | 39 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0001g0234others(36): Show | 39 | HG00741.hp1 HG01256.hp1 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.400-4809G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871677 | ||||||
| chr20:50871703
|
C | T | 6 | a0001c0001t0003g0223a0001c0001t0003g0239a0001c0001t0003g0240others(3): Show | 6 | HG01261.hp1 HG02055.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.400-4783C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871703 | ||||||
| chr20:50871727
|
C | G | 1 | a0006c0009t0001g0010 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.400-4759C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871727 | ||||||
| chr20:50871796
|
A | C | 101 | a0001c0001t0001g0179a0001c0001t0002g0017a0001c0001t0002g0071others(98): Show | 101 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.400-4690A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871796 | ||||||
| chr20:50871912
|
G | A | 101 | a0001c0001t0001g0179a0001c0001t0002g0017a0001c0001t0002g0071others(98): Show | 101 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.400-4574G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50871912 | ||||||
| chr20:50872017
|
T | C | 1 | a0001c0003t0001g0208 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.400-4469T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872017 | ||||||
| chr20:50872026
|
G | A | 1 | a0002c0002t0003g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.400-4460G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872026 | ||||||
| chr20:50872077
|
C | T | 130 | a0001c0001t0001g0075a0001c0001t0001g0179a0001c0001t0001g0212others(127): Show | 130 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.400-4409C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872077 | ||||||
| chr20:50872084
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.400-4402A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872084 | ||||||
| chr20:50872085
|
C | A | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.400-4401C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872085 | ||||||
| chr20:50872089
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.400-4397A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872089 | ||||||
| chr20:50872232
|
CCAGCCTG others(5): Show |
C | 2 | a0002c0002t0001g0027a0002c0002t0001g0037 | 2 | NA18963.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.400-4250_400-4239d others(14): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50872232 | |||||
| chr20:50872251
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0144 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.400-4235G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872251 | ||||||
| chr20:50872263
|
C | CA | 43 | a0001c0001t0001g0075a0001c0001t0001g0153a0001c0001t0001g0212others(40): Show | 43 | HG00741.hp1 HG01192.hp1 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.400-4202dupA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50872263 | |||||
| chr20:50872263
|
C | CAA | 61 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0105others(58): Show | 61 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.400-4203_400-4202d others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50872263 | |||||
| chr20:50872263
|
C | CAAA | 8 | a0001c0001t0002g0017a0001c0001t0002g0162a0001c0001t0002g0226others(5): Show | 8 | HG01106.hp2 HG01261.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-4204_400-4202d others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50872263 | |||||
| chr20:50872263
|
C | CAAAAA | 7 | a0001c0001t0005g0115a0001c0001t0005g0207a0001c0001t0005g0214others(4): Show | 7 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-4206_400-4202d others(7): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50872263 | |||||
| chr20:50872263
|
C | CAAAAAAA | 10 | a0001c0001t0001g0179a0001c0001t0004g0040a0001c0001t0004g0098others(7): Show | 10 | HG01167.hp1 HG01952.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.400-4208_400-4202d others(9): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50872263 | |||||
| chr20:50872263
|
CA | C | 111 | a0001c0001t0001g0022a0001c0001t0001g0079a0001c0001t0001g0080others(108): Show | 111 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.400-4202delA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50872263 | |||||
| chr20:50872285
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.400-4201G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872285 | ||||||
| chr20:50872286
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.400-4200A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872286 | ||||||
| chr20:50872287
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.400-4199G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872287 | ||||||
| chr20:50872293
|
G | A | 1 | a0001c0001t0006g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.400-4193G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872293 | ||||||
| chr20:50872313
|
G | T | 23 | a0001c0001t0002g0086a0001c0001t0002g0127a0001c0001t0002g0137others(20): Show | 23 | HG00741.hp1 HG01256.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.400-4173G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872313 | ||||||
| chr20:50872352
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.400-4134C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872352 | ||||||
| chr20:50872418
|
A | C | 3 | a0003c0005t0006g0082a0003c0005t0006g0084a0003c0005t0006g0085 | 3 | HG01361.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.400-4068A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872418 | ||||||
| chr20:50872515
|
T | G | 138 | a0001c0001t0001g0075a0001c0001t0001g0179a0001c0001t0001g0212others(135): Show | 138 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.400-3971T>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872515 | ||||||
| chr20:50872578
|
GAAC | G | 11 | a0001c0001t0001g0179a0001c0001t0004g0040a0001c0001t0004g0098others(8): Show | 11 | HG01167.hp1 HG01952.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.400-3905_400-3903d others(5): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50872578 | |||||
| chr20:50872579
|
AAC | A | 90 | a0001c0001t0002g0017a0001c0001t0002g0071a0001c0001t0002g0072others(87): Show | 90 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.400-3905_400-3904d others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50872579 | |||||
| chr20:50872580
|
AC | A | 37 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0001g0234others(34): Show | 37 | HG00741.hp1 HG01256.hp1 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.400-3905delC | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872580 | ||||||
| chr20:50872643
|
G | T | 144 | a0001c0001t0001g0075a0001c0001t0001g0179a0001c0001t0001g0212others(141): Show | 144 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.400-3843G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872643 | ||||||
| chr20:50872801
|
C | T | 2 | a0001c0003t0001g0094a0001c0003t0001g0133 | 2 | HG02622.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.400-3685C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872801 | ||||||
| chr20:50872818
|
C | G | 3 | a0003c0005t0006g0082a0003c0005t0006g0084a0003c0005t0006g0085 | 3 | HG01361.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.400-3668C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872818 | ||||||
| chr20:50872857
|
C | T | 1 | a0001c0001t0004g0235 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.400-3629C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872857 | ||||||
| chr20:50872983
|
G | A | 138 | a0001c0001t0001g0075a0001c0001t0001g0179a0001c0001t0001g0212others(135): Show | 138 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.400-3503G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50872983 | ||||||
| chr20:50873038
|
G | A | 2 | a0001c0001t0002g0180a0001c0001t0002g0193 | 2 | NA19056.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.400-3448G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873038 | ||||||
| chr20:50873060
|
G | A | 37 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0001g0234others(34): Show | 37 | HG00741.hp1 HG01256.hp1 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.400-3426G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873060 | ||||||
| chr20:50873209
|
T | C | 1 | a0001c0004t0003g0008 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.400-3277T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873209 | ||||||
| chr20:50873298
|
G | A | 1 | a0001c0001t0004g0235 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.400-3188G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873298 | ||||||
| chr20:50873325
|
G | T | 4 | a0001c0001t0006g0077a0003c0005t0006g0082a0003c0005t0006g0084others(1): Show | 4 | HG01361.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-3161G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873325 | ||||||
| chr20:50873439
|
C | G | 8 | a0001c0003t0001g0004a0001c0003t0001g0005a0001c0003t0001g0081others(5): Show | 8 | HG01243.hp2 HG01358.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.400-3047C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873439 | ||||||
| chr20:50873476
|
C | T | 8 | a0001c0003t0001g0004a0001c0003t0001g0005a0001c0003t0001g0081others(5): Show | 8 | HG01243.hp2 HG01358.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.400-3010C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873476 | ||||||
| chr20:50873524
|
T | C | 1 | a0002c0002t0004g0061 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.400-2962T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873524 | ||||||
| chr20:50873534
|
C | T | 31 | a0001c0001t0002g0119a0001c0001t0003g0002a0001c0001t0003g0073others(28): Show | 31 | HG00423.hp2 HG00558.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.400-2952C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873534 | ||||||
| chr20:50873579
|
C | T | 134 | a0001c0001t0001g0075a0001c0001t0001g0179a0001c0001t0001g0212others(131): Show | 134 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.400-2907C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873579 | ||||||
| chr20:50873675
|
G | A | 8 | a0001c0003t0001g0004a0001c0003t0001g0005a0001c0003t0001g0081others(5): Show | 8 | HG01243.hp2 HG01358.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.400-2811G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873675 | ||||||
| chr20:50873716
|
G | A | 1 | a0001c0004t0004g0007 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.400-2770G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50873716 | ||||||
| chr20:50874022
|
G | A | 27 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0192others(24): Show | 27 | HG01261.hp1 HG01943.hp2 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.400-2464G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50874022 | ||||||
| chr20:50874039
|
C | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0153a0002c0002t0001g0083 | 3 | HG00099.hp2 HG01192.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.400-2447C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50874039 | ||||||
| chr20:50874186
|
G | C | 1 | a0001c0001t0001g0154 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.400-2300G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50874186 | ||||||
| chr20:50874273
|
G | A | 2 | a0001c0001t0003g0222a0001c0001t0005g0214 | 2 | HG02293.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.400-2213G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50874273 | ||||||
| chr20:50874351
|
T | C | 179 | a0001c0001t0001g0075a0001c0001t0001g0144a0001c0001t0001g0212others(176): Show | 179 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.400-2135T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50874351 | ||||||
| chr20:50874384
|
G | A | 1 | a0001c0003t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.400-2102G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50874384 | ||||||
| chr20:50874399
|
C | G | 11 | a0001c0001t0001g0144a0001c0001t0003g0065a0001c0001t0005g0115others(8): Show | 11 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.400-2087C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50874399 | ||||||
| chr20:50874636
|
C | G | 11 | a0001c0001t0003g0065a0001c0001t0004g0201a0001c0001t0005g0115others(8): Show | 11 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.400-1850C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50874636 | ||||||
| chr20:50874684
|
A | C | 11 | a0001c0001t0003g0065a0001c0001t0004g0201a0001c0001t0005g0115others(8): Show | 11 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.400-1802A>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50874684 | ||||||
| chr20:50874739
|
G | C | 1 | a0001c0003t0001g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.400-1747G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50874739 | ||||||
| chr20:50874949
|
G | A | 10 | a0001c0001t0003g0065a0001c0001t0005g0115a0001c0001t0005g0200others(7): Show | 10 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-1537G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50874949 | ||||||
| chr20:50875007
|
G | A | 10 | a0001c0001t0003g0065a0001c0001t0005g0115a0001c0001t0005g0200others(7): Show | 10 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-1479G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875007 | ||||||
| chr20:50875070
|
A | G | 10 | a0001c0001t0003g0065a0001c0001t0005g0115a0001c0001t0005g0200others(7): Show | 10 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-1416A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875070 | ||||||
| chr20:50875124
|
A | G | 9 | a0001c0001t0005g0115a0001c0001t0005g0200a0001c0001t0005g0206others(6): Show | 9 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-1362A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875124 | ||||||
| chr20:50875183
|
T | C | 10 | a0001c0001t0003g0065a0001c0001t0005g0115a0001c0001t0005g0200others(7): Show | 10 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-1303T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875183 | ||||||
| chr20:50875209
|
C | A | 28 | a0001c0001t0003g0002a0001c0001t0003g0073a0001c0001t0003g0163others(25): Show | 28 | HG00408.hp2 HG01106.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.400-1277C>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875209 | ||||||
| chr20:50875231
|
G | A | 63 | a0001c0001t0002g0017a0001c0001t0002g0071a0001c0001t0002g0072others(60): Show | 63 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.400-1255G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875231 | ||||||
| chr20:50875306
|
GCA | G | 10 | a0001c0001t0003g0065a0001c0001t0005g0115a0001c0001t0005g0200others(7): Show | 10 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-1177_400-1176d others(4): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50875306 | |||||
| chr20:50875321
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.400-1165C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875321 | ||||||
| chr20:50875343
|
C | T | 97 | a0001c0001t0002g0017a0001c0001t0002g0071a0001c0001t0002g0072others(94): Show | 97 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.400-1143C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875343 | ||||||
| chr20:50875539
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.400-947C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875539 | ||||||
| chr20:50875570
|
G | A | 1 | a0002c0002t0002g0041 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.400-916G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875570 | ||||||
| chr20:50875602
|
T | TA | 96 | a0001c0001t0002g0017a0001c0001t0002g0071a0001c0001t0002g0072others(93): Show | 96 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.400-864dupA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50875602 | |||||
| chr20:50875602
|
TAAA | T | 38 | a0001c0001t0003g0002a0001c0001t0003g0065a0001c0001t0003g0073others(35): Show | 38 | HG00408.hp2 HG00642.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.400-866_400-864del others(3): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50875602 | |||||
| chr20:50875613
|
A | G | 38 | a0001c0001t0003g0002a0001c0001t0003g0065a0001c0001t0003g0073others(35): Show | 38 | HG00408.hp2 HG00642.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.400-873A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875613 | ||||||
| chr20:50875654
|
G | A | 1 | a0001c0001t0003g0073 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.400-832G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875654 | ||||||
| chr20:50875786
|
G | GA | 35 | a0001c0001t0001g0075a0001c0001t0001g0212a0001c0001t0001g0234others(32): Show | 35 | HG00408.hp2 HG01106.hp2 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.400-689dupA | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr20 | 50875786 | |||||
| chr20:50875793
|
A | AG | 9 | a0001c0001t0005g0115a0001c0001t0005g0200a0001c0001t0005g0206others(6): Show | 9 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.400-693_400-692ins others(1): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875793 | ||||||
| chr20:50875862
|
G | A | 11 | a0001c0001t0001g0188a0001c0001t0003g0065a0001c0001t0005g0115others(8): Show | 11 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.400-624G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875862 | ||||||
| chr20:50875893
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.400-593A>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875893 | ||||||
| chr20:50875921
|
C | T | 10 | a0001c0001t0003g0065a0001c0001t0005g0115a0001c0001t0005g0200others(7): Show | 10 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-565C>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50875921 | ||||||
| chr20:50876025
|
G | A | 10 | a0001c0001t0003g0065a0001c0001t0005g0115a0001c0001t0005g0200others(7): Show | 10 | HG00642.hp1 HG01167.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-461G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50876025 | ||||||
| chr20:50876054
|
G | T | 1 | a0001c0001t0003g0065 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.400-432G>T | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50876054 | ||||||
| chr20:50876086
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.400-400G>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50876086 | ||||||
| chr20:50876303
|
C | G | 1 | a0001c0001t0008g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.400-183C>G | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50876303 | ||||||
| chr20:50876330
|
CCGGCTTT others(1): Show |
C | 32 | a0001c0001t0003g0002a0001c0001t0003g0073a0001c0001t0003g0163others(29): Show | 32 | HG00408.hp2 HG01106.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.400-155_400-148del others(8): Show |
BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50876330 | ||||||
| chr20:50876374
|
T | C | 4 | a0001c0001t0006g0077a0003c0005t0006g0082a0003c0005t0006g0084others(1): Show | 4 | HG01361.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-112T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50876374 | ||||||
| chr20:50876391
|
G | C | 33 | a0001c0001t0003g0002a0001c0001t0003g0073a0001c0001t0003g0163others(30): Show | 33 | HG00408.hp2 HG01106.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.400-95G>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50876391 | ||||||
| chr20:50876466
|
T | A | 42 | a0001c0001t0003g0002a0001c0001t0003g0065a0001c0001t0003g0073others(39): Show | 42 | HG00408.hp2 HG00642.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.400-20T>A | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50876466 | ||||||
| chr20:50876467
|
T | C | 42 | a0001c0001t0003g0002a0001c0001t0003g0065a0001c0001t0003g0073others(39): Show | 42 | HG00408.hp2 HG00642.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.400-19T>C | BCAS4 | ENSG00000124243.19 | transcript | ENST00000371608.8 | protein_coding | 4/4 | chr20 | 50876467 |