Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9139 |
|---|---|
| ensemblid | ENSG00000078699.22 |
| hgncid | 1536 |
| symbol | CBFA2T2 |
| name | CBFA2/RUNX1 partner transcriptional co-repressor 2 |
| refseq_nuc | NM_001032999.3 |
| refseq_prot | NP_001028171.1 |
| ensembl_nuc | ENST00000342704.11 |
| ensembl_prot | ENSP00000345810.6 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 33490096 |
| end | 33650030 |
| strand | + |
| ver | v1.2 |
| region | chr20:33490096-33650030 |
| region5000 | chr20:33485096-33655030 |
| regionname0 | CBFA2T2_chr20_33490096_33650030 |
| regionname5000 | CBFA2T2_chr20_33485096_33655030 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 595 | 295 | 81 | 50 | 110 | 12 | 40 | 80 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0002 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0003 | 0/0 | 595 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0004 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1788 | 205 | 72 | 32 | 71 | 8 | 22 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| c0002 | 1/1 | 1788 | 70 | 6 | 16 | 27 | 4 | 15 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| c0003 | 0/0 | 1788 | 11 | 0 | 0 | 11 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| c0004 | 0/0 | 1788 | 4 | 1 | 1 | 0 | 0 | 2 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| c0005 | 0/0 | 1788 | 3 | 0 | 1 | 1 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| c0006 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| c0007 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| c0008 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| c0009 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| c0010 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5558 | 61 | 3 | 9 | 40 | 2 | 7 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0002 | 1/0 | 5557 | 59 | 6 | 15 | 25 | 4 | 8 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0003 | 0/0 | 5556 | 43 | 7 | 6 | 20 | 5 | 5 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0004 | 0/0 | 5556 | 29 | 10 | 10 | 7 | 0 | 2 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0005 | 0/0 | 5556 | 15 | 15 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0006 | 0/0 | 5556 | 12 | 0 | 2 | 4 | 1 | 5 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0007 | 0/0 | 5556 | 8 | 8 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0008 | 0/0 | 5554 | 6 | 5 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0009 | 0/1 | 5558 | 6 | 0 | 0 | 1 | 0 | 4 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0010 | 0/0 | 5557 | 5 | 0 | 1 | 4 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0011 | 0/0 | 5552 | 4 | 4 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0012 | 0/0 | 5564 | 4 | 3 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0013 | 0/0 | 5557 | 3 | 3 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0014 | 0/0 | 5556 | 3 | 1 | 0 | 1 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0015 | 0/0 | 5556 | 3 | 3 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0016 | 0/0 | 5557 | 3 | 0 | 1 | 0 | 0 | 2 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0017 | 0/0 | 5557 | 2 | 0 | 0 | 2 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0018 | 0/0 | 5556 | 2 | 2 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0019 | 0/0 | 5556 | 2 | 0 | 0 | 2 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0020 | 0/0 | 5557 | 2 | 0 | 1 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0021 | 0/0 | 5557 | 2 | 0 | 0 | 0 | 0 | 2 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0022 | 0/0 | 5558 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0023 | 0/0 | 5556 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0024 | 0/0 | 5557 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0025 | 0/0 | 5556 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0026 | 0/0 | 5557 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0027 | 0/0 | 5557 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0028 | 0/0 | 5557 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0029 | 0/0 | 5556 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0030 | 0/0 | 5557 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0031 | 0/0 | 5557 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0032 | 0/0 | 5556 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0033 | 0/0 | 5558 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0034 | 0/0 | 5557 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0035 | 0/0 | 5558 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0036 | 0/0 | 5556 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0037 | 0/0 | 5556 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0038 | 0/0 | 5556 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0039 | 0/0 | 5557 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0040 | 0/0 | 5557 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0041 | 0/0 | 5558 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0042 | 0/0 | 5558 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0043 | 0/0 | 5557 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0044 | 0/0 | 5556 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| t0045 | 0/0 | 5558 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1788 | 205 | 72 | 32 | 71 | 8 | 22 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0002 | 1/1 | 1788 | 70 | 6 | 16 | 27 | 4 | 15 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0003 | 0/0 | 1788 | 11 | 0 | 0 | 11 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0004 | 0/0 | 1788 | 4 | 1 | 1 | 0 | 0 | 2 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0005 | 0/0 | 1788 | 3 | 0 | 1 | 1 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0006 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0010 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0002c0008 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0003c0009 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0004c0007 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7345 | 50 | 3 | 9 | 29 | 2 | 7 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0003 | 0/0 | 7343 | 43 | 7 | 6 | 20 | 5 | 5 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0004 | 0/0 | 7343 | 29 | 10 | 10 | 7 | 0 | 2 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0005 | 0/0 | 7343 | 15 | 15 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0006 | 0/0 | 7343 | 9 | 0 | 1 | 4 | 1 | 3 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0007 | 0/0 | 7343 | 7 | 7 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0008 | 0/0 | 7341 | 6 | 5 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0010 | 0/0 | 7344 | 5 | 0 | 1 | 4 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0011 | 0/0 | 7339 | 4 | 4 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0012 | 0/0 | 7351 | 4 | 3 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0013 | 0/0 | 7344 | 3 | 3 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0014 | 0/0 | 7343 | 3 | 1 | 0 | 1 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0015 | 0/0 | 7343 | 3 | 3 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0017 | 0/0 | 7344 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0018 | 0/0 | 7343 | 2 | 2 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0019 | 0/0 | 7343 | 2 | 0 | 0 | 2 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0020 | 0/0 | 7344 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0021 | 0/0 | 7344 | 2 | 0 | 0 | 0 | 0 | 2 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0022 | 0/0 | 7345 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0023 | 0/0 | 7343 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0025 | 0/0 | 7343 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0026 | 0/0 | 7344 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0030 | 0/0 | 7344 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0031 | 0/0 | 7344 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0032 | 0/0 | 7343 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0033 | 0/0 | 7345 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0036 | 0/0 | 7343 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0037 | 0/0 | 7343 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0038 | 0/0 | 7343 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0039 | 0/0 | 7344 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0040 | 0/0 | 7344 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0041 | 0/0 | 7345 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0042 | 0/0 | 7345 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0001t0043 | 0/0 | 7344 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0002t0002 | 1/0 | 7344 | 54 | 6 | 14 | 22 | 4 | 7 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0002t0009 | 0/1 | 7345 | 6 | 0 | 0 | 1 | 0 | 4 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0002t0016 | 0/0 | 7344 | 3 | 0 | 1 | 0 | 0 | 2 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0002t0017 | 0/0 | 7344 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0002t0020 | 0/0 | 7344 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0002t0024 | 0/0 | 7344 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0002t0027 | 0/0 | 7344 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0002t0034 | 0/0 | 7344 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0002t0035 | 0/0 | 7345 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0002t0045 | 0/0 | 7345 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0003t0001 | 0/0 | 7345 | 11 | 0 | 0 | 11 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0004t0006 | 0/0 | 7343 | 3 | 0 | 1 | 0 | 0 | 2 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0004t0044 | 0/0 | 7343 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0005t0002 | 0/0 | 7344 | 3 | 0 | 1 | 1 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0006t0007 | 0/0 | 7343 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0001c0010t0028 | 0/0 | 7344 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0002c0008t0002 | 0/0 | 7344 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0003c0009t0029 | 0/0 | 7343 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| a0004c0007t0002 | 0/0 | 7344 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | copy fasta | chr20 | 33485096 | 33655030 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0010g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0010g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0010g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0010g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0010g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0011g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0012g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0012g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0013g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0014g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0014g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0014g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0017g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0018g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0018g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0019g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0019g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0020g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0021g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0021g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0022g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0023g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0025g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0026g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0030g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0031g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0032g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0033g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0036g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0037g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0038g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0039g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0040g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0041g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0042g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0001t0043g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0009g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0009g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0009g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0009g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0009g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0009g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0016g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0016g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0016g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0017g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0020g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0024g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0027g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0034g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0035g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0002t0045g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0004t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0004t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0004t0006g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0004t0044g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0005t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0005t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0005t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0006t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0001c0010t0028g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0002c0008t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0003c0009t0029g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| a0004c0007t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0177 | EUR | GBR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0110 | EUR | GBR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0161 | EUR | FIN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0089 | EUR | FIN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00408 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0095 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00639 | hp1 | a0001 | c0005 | t0002 | g0179 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0134 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0204 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0201 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00741 | hp1 | a0001 | c0001 | t0020 | g0160 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0208 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0168 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0207 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0166 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01167 | hp2 | a0001 | c0001 | t0012 | g0162 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01243 | hp2 | a0001 | c0001 | t0039 | g0137 | AMR | PUR | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01255 | hp2 | a0001 | c0002 | t0016 | g0193 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0188 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0189 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01261 | hp1 | a0001 | c0001 | t0041 | g0273 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01261 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0192 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0091 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0210 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0072 | EUR | IBS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0183 | EUR | IBS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | IBS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0141 | EUR | IBS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | IBS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0071 | EUR | IBS | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01884 | hp1 | a0001 | c0001 | t0025 | g0009 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0191 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0211 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01891 | hp2 | a0001 | c0001 | t0018 | g0120 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | PEL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0203 | AMR | PEL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PEL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0174 | AMR | PEL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02080 | hp2 | a0001 | c0001 | t0010 | g0151 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02083 | hp2 | a0001 | c0005 | t0002 | g0186 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02135 | hp1 | a0001 | c0001 | t0017 | g0102 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0133 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02148 | hp1 | a0001 | c0002 | t0035 | g0202 | AMR | PEL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02148 | hp2 | a0001 | c0001 | t0010 | g0114 | AMR | PEL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | CDX | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | CDX | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0181 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PEL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | KHV | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02622 | hp2 | a0001 | c0001 | t0026 | g0198 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02630 | hp2 | a0001 | c0001 | t0032 | g0070 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0054 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0157 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0265 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0187 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0214 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0061 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02809 | hp1 | a0001 | c0010 | t0028 | g0132 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0003 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0066 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0206 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02886 | hp2 | a0003 | c0009 | t0029 | g0283 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0063 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0064 | AFR | GWD | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02922 | hp2 | a0001 | c0001 | t0018 | g0121 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02970 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03017 | hp2 | a0001 | c0002 | t0009 | g0218 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0138 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0080 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03130 | hp2 | a0001 | c0001 | t0037 | g0296 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0130 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0292 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0293 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0084 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0165 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03486 | hp1 | a0001 | c0001 | t0013 | g0199 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03490 | hp1 | a0001 | c0002 | t0009 | g0172 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03490 | hp2 | a0001 | c0004 | t0006 | g0093 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03491 | hp1 | a0001 | c0002 | t0024 | g0074 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03491 | hp2 | a0001 | c0001 | t0014 | g0184 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03492 | hp1 | a0001 | c0002 | t0009 | g0173 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0136 | AFR | ESN | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0146 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03579 | hp2 | a0001 | c0001 | t0030 | g0001 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03654 | hp1 | a0001 | c0001 | t0023 | g0076 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03654 | hp2 | a0001 | c0002 | t0016 | g0190 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03669 | hp1 | a0001 | c0001 | t0043 | g0221 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0185 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0215 | SAS | STU | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03688 | hp2 | a0001 | c0001 | t0021 | g0278 | SAS | STU | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0143 | SAS | BEB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03831 | hp2 | a0001 | c0002 | t0045 | g0216 | SAS | BEB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0113 | SAS | BEB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0205 | SAS | STU | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG04184 | hp1 | a0001 | c0002 | t0009 | g0217 | SAS | BEB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG04184 | hp2 | a0001 | c0004 | t0006 | g0142 | SAS | BEB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | STU | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0294 | SAS | STU | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | STU | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG04204 | hp2 | a0001 | c0005 | t0002 | g0182 | SAS | STU | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0112 | SAS | STU | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | YRI | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0164 | AFR | YRI | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | CHB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | CHB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | YRI | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0212 | AFR | YRI | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18939 | hp2 | a0001 | c0001 | t0038 | g0116 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0281 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18943 | hp1 | a0001 | c0001 | t0014 | g0032 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18943 | hp2 | a0001 | c0002 | t0017 | g0124 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18968 | hp1 | a0001 | c0003 | t0001 | g0226 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18969 | hp1 | a0004 | c0007 | t0002 | g0055 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18969 | hp2 | a0001 | c0001 | t0022 | g0103 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18970 | hp1 | a0001 | c0001 | t0010 | g0088 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18971 | hp1 | a0001 | c0001 | t0019 | g0117 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18979 | hp2 | a0001 | c0002 | t0027 | g0213 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18983 | hp1 | a0001 | c0002 | t0034 | g0043 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0266 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA18998 | hp2 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19001 | hp1 | a0001 | c0002 | t0020 | g0271 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19001 | hp2 | a0001 | c0001 | t0033 | g0052 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19030 | hp1 | a0001 | c0001 | t0031 | g0068 | AFR | LWK | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0015 | AFR | LWK | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19060 | hp2 | a0001 | c0001 | t0010 | g0075 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19063 | hp1 | a0001 | c0003 | t0001 | g0232 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19063 | hp2 | a0001 | c0001 | t0010 | g0150 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19074 | hp1 | a0002 | c0008 | t0002 | g0047 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19075 | hp1 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19075 | hp2 | a0001 | c0001 | t0019 | g0082 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19079 | hp1 | a0001 | c0002 | t0009 | g0290 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0233 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19086 | hp2 | a0001 | c0003 | t0001 | g0297 | EAS | JPT | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | YRI | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA19240 | hp2 | a0001 | c0001 | t0015 | g0016 | AFR | YRI | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0073 | EUR | TSI | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0178 | EUR | TSI | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA20905 | hp1 | a0001 | c0002 | t0016 | g0170 | SAS | GIH | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0083 | SAS | GIH | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0180 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG01123 | hp2 | a0001 | c0004 | t0006 | g0140 | AMR | CLM | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02109 | hp1 | a0001 | c0004 | t0044 | g0092 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02109 | hp2 | a0001 | c0001 | t0040 | g0295 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0163 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0062 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG02559 | hp2 | a0001 | c0006 | t0007 | g0282 | AFR | ACB | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0197 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0196 | AFR | MSL | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0291 | AFR | USA | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | USA | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | USA | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | USA | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA21309 | hp1 | a0001 | c0001 | t0036 | g0018 | AFR | LWK | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| NA21309 | hp2 | a0001 | c0001 | t0042 | g0194 | AFR | LWK | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0009 | g0219 | REF | REF | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0065 | REF | REF | CBFA2T2_chr20_33485096_33655030 | CBFA2T2 | chr20 | 33485096 | 33655030 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:33606988
|
G | A | 1 | a0004 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.67G>A | p.Gly23Arg | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/11 | 239/7344 | 67/1788 | 23/595 | chr20 | 33606988 | ||
| chr20:33629858
|
G | A | 1 | a0002 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.1172G>A | p.Gly391Glu | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/11 | 1344/7344 | 1172/1788 | 391/595 | chr20 | 33629858 | ||
| chr20:33644574
|
C | G | 1 | a0003 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1716C>G | p.Asp572Glu | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 1888/7344 | 1716/1788 | 572/595 | chr20 | 33644574 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:33490273
|
A | G | 1 | a0001c0010 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.6A>G | p.Val2Val | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/11 | 178/7344 | 6/1788 | 2/595 | chr20 | 33490273 | ||
| chr20:33490300
|
G | A | 1 | a0001c0006 | 1 | HG02559.hp2 | splice_region_variant&synonymous_variant | LOW | c.33G>A | p.Gln11Gln | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/11 | 205/7344 | 33/1788 | 11/595 | chr20 | 33490300 | ||
| chr20:33611125
|
C | G | 2 | a0001c0006a0001c0010 | 2 | HG02559.hp2 HG02809.hp1 |
synonymous_variant | LOW | c.210C>G | p.Thr70Thr | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/11 | 382/7344 | 210/1788 | 70/595 | chr20 | 33611125 | ||
| chr20:33623264
|
G | A | 1 | a0001c0005 | 3 | HG00639.hp1 HG02083.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.660G>A | p.Val220Val | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/11 | 832/7344 | 660/1788 | 220/595 | chr20 | 33623264 | ||
| chr20:33624884
|
C | T | 6 | a0001c0001a0001c0003a0001c0004others(3): Show | 223 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
synonymous_variant | LOW | c.813C>T | p.Pro271Pro | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/11 | 985/7344 | 813/1788 | 271/595 | chr20 | 33624884 | ||
| chr20:33640393
|
C | G | 1 | a0001c0003 | 11 | NA18941.hp1 NA18968.hp1 NA18982.hp2 others(8): Show |
synonymous_variant | LOW | c.1350C>G | p.Ala450Ala | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/11 | 1522/7344 | 1350/1788 | 450/595 | chr20 | 33640393 | ||
| chr20:33644490
|
C | T | 1 | a0001c0004 | 4 | HG01123.hp2 HG02109.hp1 HG03490.hp2 others(1): Show |
synonymous_variant | LOW | c.1632C>T | p.His544His | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 1804/7344 | 1632/1788 | 544/595 | chr20 | 33644490 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:33490105
|
G | T | 1 | a0001c0002t0045 | 1 | HG03831.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-163G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/11 | chr20 | 33490105 | ||||||
| chr20:33490109
|
A | G | 1 | a0001c0004t0044 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-159A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/11 | 159 | chr20 | 33490109 | |||||
| chr20:33490110
|
C | A | 8 | a0001c0001t0003a0001c0001t0010a0001c0001t0017others(5): Show | 55 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(52): Show |
5_prime_UTR_variant | MODIFIER | c.-158C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/11 | 158 | chr20 | 33490110 | |||||
| chr20:33490119
|
C | T | 26 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(23): Show | 161 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(158): Show |
5_prime_UTR_variant | MODIFIER | c.-149C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/11 | 149 | chr20 | 33490119 | |||||
| chr20:33490144
|
C | T | 1 | a0001c0001t0036 | 1 | NA21309.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-124C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/11 | chr20 | 33490144 | ||||||
| chr20:33490236
|
A | AGGCGGGC | 1 | a0001c0001t0012 | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-27_-21dupGGCGGCG | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/11 | 20 | INFO_REALIGN_3_PRIME | chr20 | 33490236 | ||||
| chr20:33644692
|
G | A | 1 | a0001c0001t0037 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*46G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 46 | chr20 | 33644692 | |||||
| chr20:33644767
|
A | G | 3 | a0001c0002t0016a0001c0002t0024a0001c0002t0035 | 5 | HG01255.hp2 HG02148.hp1 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*121A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 121 | chr20 | 33644767 | |||||
| chr20:33644790
|
T | C | 2 | a0001c0001t0019a0001c0001t0038 | 3 | NA18939.hp2 NA18971.hp1 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*144T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 144 | chr20 | 33644790 | |||||
| chr20:33644828
|
G | C | 2 | a0001c0001t0008a0001c0001t0025 | 7 | HG01261.hp2 HG01884.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*182G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 182 | chr20 | 33644828 | |||||
| chr20:33645096
|
C | T | 1 | a0001c0002t0034 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*450C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 450 | chr20 | 33645096 | |||||
| chr20:33645133
|
C | T | 1 | a0001c0001t0018 | 2 | HG01891.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*487C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 487 | chr20 | 33645133 | |||||
| chr20:33645143
|
G | T | 7 | a0001c0001t0001a0001c0001t0021a0001c0001t0033others(4): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*497G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 497 | chr20 | 33645143 | |||||
| chr20:33645263
|
TA | T | 27 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(24): Show | 145 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*621delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 621 | INFO_REALIGN_3_PRIME | chr20 | 33645263 | ||||
| chr20:33645303
|
G | A | 1 | a0001c0001t0026 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*657G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 657 | chr20 | 33645303 | |||||
| chr20:33645341
|
G | A | 1 | a0001c0002t0027 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*695G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 695 | chr20 | 33645341 | |||||
| chr20:33645529
|
A | G | 1 | a0001c0001t0032 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*883A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 883 | chr20 | 33645529 | |||||
| chr20:33645587
|
C | T | 1 | a0001c0001t0019 | 2 | NA18971.hp1 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*941C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 941 | chr20 | 33645587 | |||||
| chr20:33645865
|
A | G | 1 | a0001c0001t0037 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1219A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 1219 | chr20 | 33645865 | |||||
| chr20:33646003
|
G | T | 5 | a0001c0001t0004a0001c0001t0015a0001c0001t0031others(2): Show | 35 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1357G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 1357 | chr20 | 33646003 | |||||
| chr20:33646011
|
G | T | 13 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(10): Show | 57 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1365G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 1365 | chr20 | 33646011 | |||||
| chr20:33646077
|
C | T | 1 | a0001c0001t0030 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1431C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 1431 | chr20 | 33646077 | |||||
| chr20:33646195
|
G | C | 1 | a0001c0001t0041 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1549G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 1549 | chr20 | 33646195 | |||||
| chr20:33646419
|
C | T | 2 | a0001c0001t0013a0001c0001t0026 | 4 | HG02622.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1773C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 1773 | chr20 | 33646419 | |||||
| chr20:33646820
|
C | G | 1 | a0001c0001t0023 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2174C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 2174 | chr20 | 33646820 | |||||
| chr20:33646860
|
C | CA | 16 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(13): Show | 87 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2231dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 2232 | INFO_REALIGN_3_PRIME | chr20 | 33646860 | ||||
| chr20:33647140
|
G | A | 1 | a0001c0001t0015 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2494G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 2494 | chr20 | 33647140 | |||||
| chr20:33647236
|
A | T | 2 | a0001c0001t0031a0001c0001t0032 | 2 | HG02630.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2590A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 2590 | chr20 | 33647236 | |||||
| chr20:33647516
|
T | C | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2870T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 2870 | chr20 | 33647516 | |||||
| chr20:33647982
|
ACT | A | 1 | a0001c0001t0008 | 6 | HG01261.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3341_*3342delCT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 3341 | INFO_REALIGN_3_PRIME | chr20 | 33647982 | ||||
| chr20:33648015
|
C | T | 1 | a0001c0001t0030 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3369C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 3369 | chr20 | 33648015 | |||||
| chr20:33648815
|
T | G | 3 | a0001c0001t0005a0001c0001t0037a0001c0001t0039 | 17 | HG01243.hp2 HG02145.hp1 HG02647.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4169T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 4169 | chr20 | 33648815 | |||||
| chr20:33648888
|
C | T | 1 | a0001c0001t0021 | 2 | HG02735.hp1 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4242C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 4242 | chr20 | 33648888 | |||||
| chr20:33649124
|
C | T | 1 | a0003c0009t0029 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4478C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 4478 | chr20 | 33649124 | |||||
| chr20:33649360
|
G | A | 1 | a0001c0010t0028 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4714G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 4714 | chr20 | 33649360 | |||||
| chr20:33649406
|
G | C | 2 | a0001c0001t0031a0001c0001t0032 | 2 | HG02630.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4760G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 4760 | chr20 | 33649406 | |||||
| chr20:33649448
|
C | T | 1 | a0001c0001t0030 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4802C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 4802 | chr20 | 33649448 | |||||
| chr20:33649495
|
C | T | 1 | a0001c0001t0042 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4849C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 4849 | chr20 | 33649495 | |||||
| chr20:33650000
|
TTAAAG | T | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5357_*5361delAAGT others(1): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 11/11 | 5357 | INFO_REALIGN_3_PRIME | chr20 | 33650000 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:33490457
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.34+156C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33490457 | ||||||
| chr20:33490612
|
C | G | 1 | a0001c0003t0001g0297 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.34+311C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33490612 | ||||||
| chr20:33490659
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+358G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33490659 | ||||||
| chr20:33490670
|
A | G | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+369A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33490670 | ||||||
| chr20:33490698
|
C | T | 1 | a0001c0002t0002g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.34+397C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33490698 | ||||||
| chr20:33490721
|
C | G | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+420C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33490721 | ||||||
| chr20:33490755
|
T | C | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+454T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33490755 | ||||||
| chr20:33490904
|
C | G | 2 | a0001c0001t0004g0291a0001c0001t0004g0292 | 2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.34+603C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33490904 | ||||||
| chr20:33491225
|
A | G | 7 | a0001c0002t0002g0284a0001c0002t0002g0285a0001c0002t0002g0286others(4): Show | 7 | NA18944.hp1 NA18994.hp2 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.34+924A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33491225 | ||||||
| chr20:33491740
|
C | T | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.34+1439C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33491740 | ||||||
| chr20:33491782
|
A | G | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+1481A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33491782 | ||||||
| chr20:33491986
|
G | A | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.34+1685G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33491986 | ||||||
| chr20:33491999
|
C | T | 133 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(130): Show | 133 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.34+1698C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33491999 | ||||||
| chr20:33492216
|
A | G | 1 | a0001c0001t0015g0016 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.34+1915A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33492216 | ||||||
| chr20:33492219
|
A | T | 1 | a0001c0001t0003g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.34+1918A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33492219 | ||||||
| chr20:33492243
|
C | T | 1 | a0001c0001t0006g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.34+1942C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33492243 | ||||||
| chr20:33492249
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.34+1948C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33492249 | ||||||
| chr20:33492294
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.34+1993C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33492294 | ||||||
| chr20:33492309
|
A | G | 238 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.34+2008A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33492309 | ||||||
| chr20:33492344
|
T | C | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.34+2043T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33492344 | ||||||
| chr20:33492415
|
T | TAA | 47 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(44): Show | 47 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.34+2123_34+2124dup others(2): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33492415 | |||||
| chr20:33492433
|
T | TCCAAATT others(307): Show |
2 | a0001c0001t0004g0029a0001c0001t0004g0030 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.34+2145_34+2146ins others(314): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33492433 | |||||
| chr20:33492433
|
T | TCCAAATT others(321): Show |
12 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(9): Show | 12 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.34+2145_34+2146ins others(328): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33492433 | |||||
| chr20:33492433
|
T | TCCAAATT others(322): Show |
12 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(9): Show | 12 | HG01981.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+2145_34+2146ins others(329): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33492433 | |||||
| chr20:33492433
|
T | TCCAAATT others(324): Show |
2 | a0001c0001t0004g0056a0004c0007t0002g0055 | 2 | NA18969.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.34+2145_34+2146ins others(331): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33492433 | |||||
| chr20:33492433
|
T | TCCAAATT others(325): Show |
2 | a0001c0001t0004g0058a0001c0002t0002g0057 | 2 | HG01175.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.34+2145_34+2146ins others(332): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33492433 | |||||
| chr20:33492433
|
T | TCCAAATT others(327): Show |
1 | a0001c0002t0002g0059 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.34+2145_34+2146ins others(334): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33492433 | |||||
| chr20:33492433
|
T | TCCAAATT others(328): Show |
2 | a0001c0001t0004g0061a0001c0002t0002g0060 | 2 | HG02738.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.34+2145_34+2146ins others(335): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33492433 | |||||
| chr20:33492502
|
A | G | 65 | a0001c0001t0001g0159a0001c0001t0001g0220a0001c0001t0001g0222others(62): Show | 65 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.34+2201A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33492502 | ||||||
| chr20:33492570
|
A | G | 4 | a0001c0002t0009g0217a0001c0002t0009g0218a0001c0002t0009g0219others(1): Show | 4 | HG03017.hp2 HG03831.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+2269A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33492570 | ||||||
| chr20:33493018
|
T | C | 1 | a0001c0002t0002g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.34+2717T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33493018 | ||||||
| chr20:33493068
|
G | GT | 74 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(71): Show | 74 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.34+2791dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33493068 | |||||
| chr20:33493068
|
G | GTT | 7 | a0001c0001t0014g0293a0001c0001t0015g0014a0001c0001t0015g0015others(4): Show | 7 | HG02559.hp1 HG02630.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+2790_34+2791dup others(2): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33493068 | |||||
| chr20:33493068
|
G | T | 1 | a0001c0002t0002g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.34+2767G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33493068 | ||||||
| chr20:33493068
|
GT | G | 8 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01167.hp2 HG02486.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.34+2791delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33493068 | |||||
| chr20:33493070
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.34+2769T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33493070 | ||||||
| chr20:33493073
|
T | G | 3 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064 | 3 | HG02486.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.34+2772T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33493073 | ||||||
| chr20:33493077
|
T | TG | 5 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(2): Show | 5 | HG01261.hp2 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+2776_34+2777ins others(1): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33493077 | ||||||
| chr20:33493296
|
G | C | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+2995G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33493296 | ||||||
| chr20:33493327
|
C | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+3026C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33493327 | ||||||
| chr20:33493337
|
A | T | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+3036A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33493337 | ||||||
| chr20:33493697
|
T | C | 33 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(30): Show | 33 | HG00438.hp1 HG01070.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.34+3396T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33493697 | ||||||
| chr20:33493784
|
A | AGCCTCTA others(3): Show |
221 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.34+3486_34+3487ins others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33493784 | |||||
| chr20:33493787
|
C | CTCTACTG others(3): Show |
1 | a0001c0002t0027g0213 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.34+3486_34+3487ins others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33493787 | ||||||
| chr20:33494232
|
CATATATA others(5): Show |
C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+3940_34+3951del others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494232 | |||||
| chr20:33494239
|
ATG | A | 31 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0235others(28): Show | 31 | HG00597.hp1 HG00621.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.34+3942_34+3943del others(2): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494239 | |||||
| chr20:33494241
|
GTGTA | G | 14 | a0001c0001t0001g0239a0001c0001t0001g0259a0001c0001t0001g0269others(11): Show | 14 | HG00544.hp2 HG01070.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.34+3942_34+3945del others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494241 | |||||
| chr20:33494241
|
GTGTATA | G | 4 | a0001c0001t0001g0236a0001c0001t0005g0125a0001c0001t0006g0091others(1): Show | 4 | HG01361.hp2 HG02109.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+3942_34+3947del others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494241 | |||||
| chr20:33494243
|
G | A | 189 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0222others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.34+3942G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494243 | ||||||
| chr20:33494243
|
G | GTGTATAT others(5): Show |
1 | a0001c0001t0004g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.34+3943_34+3944ins others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494243 | |||||
| chr20:33494243
|
G | GTGTATAT others(11): Show |
1 | a0001c0001t0004g0058 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.34+3943_34+3944ins others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494243 | |||||
| chr20:33494243
|
G | GTGTGTAT others(5): Show |
1 | a0001c0001t0004g0051 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.34+3943_34+3944ins others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494243 | |||||
| chr20:33494243
|
G | GTGTGTAT others(11): Show |
1 | a0001c0001t0004g0056 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.34+3943_34+3944ins others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494243 | |||||
| chr20:33494243
|
GTATATAT others(3): Show |
G | 4 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016others(1): Show | 4 | HG02559.hp1 HG02630.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+3964_34+3973del others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494243 | |||||
| chr20:33494243
|
GTATATAT others(5): Show |
G | 1 | a0001c0001t0007g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.34+3962_34+3973del others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494243 | |||||
| chr20:33494245
|
A | G | 11 | a0001c0001t0004g0028a0001c0001t0004g0037a0001c0001t0004g0038others(8): Show | 11 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.34+3944A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494245 | ||||||
| chr20:33494247
|
A | T | 1 | a0001c0001t0001g0224 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.34+3946A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494247 | ||||||
| chr20:33494255
|
A | G | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+3954A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494255 | ||||||
| chr20:33494255
|
ATATATAT others(18): Show |
A | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+3956_34+3980del others(25): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494255 | |||||
| chr20:33494258
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0003g0131 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.34+3958_34+3968del others(11): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494258 | ||||||
| chr20:33494264
|
TATATA | T | 6 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0263others(3): Show | 6 | HG00558.hp2 HG02083.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.34+3964_34+3968del others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494264 | ||||||
| chr20:33494266
|
TA | T | 4 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0128others(1): Show | 4 | HG03486.hp1 NA18956.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+3966delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494266 | ||||||
| chr20:33494266
|
TATA | T | 12 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0279others(9): Show | 12 | HG01891.hp1 HG03471.hp2 HG03710.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+3966_34+3968del others(3): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494266 | ||||||
| chr20:33494266
|
TATATA | T | 16 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0250others(13): Show | 16 | HG00741.hp1 HG01243.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+3966_34+3970del others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494266 | ||||||
| chr20:33494267
|
A | AT | 3 | a0001c0001t0003g0154a0001c0001t0003g0156a0001c0002t0017g0124 | 3 | HG00621.hp1 HG03710.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.34+3967dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494267 | |||||
| chr20:33494267
|
A | T | 1 | a0001c0001t0003g0129 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.34+3966A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494267 | ||||||
| chr20:33494267
|
ATATATAT others(8): Show |
A | 8 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(5): Show | 8 | HG00099.hp2 HG01074.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.34+3968_34+3982del others(15): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494267 | |||||
| chr20:33494267
|
ATATATAT others(9): Show |
A | 1 | a0001c0001t0003g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.34+3968_34+3983del others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494267 | |||||
| chr20:33494268
|
TA | T | 9 | a0001c0001t0018g0120a0001c0001t0018g0121a0001c0001t0030g0001others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.34+3968delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494268 | ||||||
| chr20:33494268
|
TATA | T | 35 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242others(32): Show | 35 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.34+3968_34+3970del others(3): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494268 | ||||||
| chr20:33494268
|
TATATA | T | 6 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0003g0153others(3): Show | 6 | HG02300.hp2 HG02970.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.34+3968_34+3972del others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494268 | ||||||
| chr20:33494269
|
A | AT | 6 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0007g0069others(3): Show | 6 | HG00408.hp1 HG02080.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.34+3969dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494269 | |||||
| chr20:33494269
|
A | ATT | 3 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108 | 3 | NA18965.hp2 NA18968.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.34+3969_34+3970ins others(2): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494269 | |||||
| chr20:33494269
|
A | T | 25 | a0001c0001t0003g0122a0001c0001t0003g0123a0001c0001t0003g0126others(22): Show | 25 | HG00621.hp1 HG01255.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.34+3968A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494269 | ||||||
| chr20:33494269
|
ATATAT | A | 6 | a0001c0001t0006g0094a0001c0001t0006g0095a0001c0001t0006g0141others(3): Show | 6 | HG00408.hp2 HG00544.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.34+3970_34+3974del others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494269 | |||||
| chr20:33494269
|
ATATATTT others(3): Show |
A | 1 | a0001c0001t0003g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.34+3970_34+3979del others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494269 | |||||
| chr20:33494269
|
ATATATTT others(6): Show |
A | 1 | a0001c0001t0003g0090 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.34+3970_34+3982del others(13): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494269 | |||||
| chr20:33494269
|
ATATATTT others(8): Show |
A | 1 | a0001c0001t0003g0089 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.34+3970_34+3984del others(15): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494269 | |||||
| chr20:33494270
|
TA | T | 13 | a0001c0001t0001g0268a0001c0001t0001g0298a0001c0001t0003g0097others(10): Show | 13 | HG00597.hp2 HG02080.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.34+3970delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494270 | ||||||
| chr20:33494270
|
TATA | T | 16 | a0001c0001t0001g0224a0001c0001t0003g0096a0001c0001t0005g0146others(13): Show | 16 | HG00438.hp2 HG00738.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+3970_34+3972del others(3): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494270 | ||||||
| chr20:33494271
|
A | AT | 6 | a0001c0001t0001g0228a0001c0001t0003g0087a0001c0001t0010g0088others(3): Show | 6 | HG02486.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.34+3971dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494271 | |||||
| chr20:33494271
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0004g0292 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.34+3971_34+3972ins others(11): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494271 | |||||
| chr20:33494271
|
A | T | 91 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0249others(88): Show | 91 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.34+3970A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494271 | ||||||
| chr20:33494272
|
TA | T | 7 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086others(4): Show | 7 | HG02523.hp2 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+3972delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494272 | ||||||
| chr20:33494273
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0003g0071a0001c0001t0003g0072 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.34+3973_34+3974ins others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.34+3973_34+3974ins others(13): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0008g0002 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.34+3973_34+3974ins others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0008g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.34+3973_34+3974ins others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0004g0024 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.34+3973_34+3974ins others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATATATTT others(4): Show |
1 | a0001c0001t0004g0017 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.34+3973_34+3974ins others(11): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATATATTT others(5): Show |
2 | a0001c0001t0004g0028a0001c0001t0036g0018 | 2 | HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.34+3973_34+3974ins others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATATATTT others(6): Show |
2 | a0001c0001t0004g0019a0001c0001t0004g0025 | 2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.34+3973_34+3974ins others(13): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATATATTT others(7): Show |
2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG00738.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.34+3973_34+3974ins others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATATATTT others(8): Show |
1 | a0001c0001t0004g0022 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.34+3973_34+3974ins others(15): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATATTTTT others(4): Show |
1 | a0001c0001t0004g0026 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.34+3973_34+3974ins others(11): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATATTTTT others(5): Show |
1 | a0001c0001t0004g0023 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.34+3973_34+3974ins others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0004g0291 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.34+3989_34+3998dup others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33494273 | |||||
| chr20:33494273
|
A | T | 176 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(173): Show | 176 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.34+3972A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494273 | ||||||
| chr20:33494274
|
T | TATATATA others(4): Show |
3 | a0001c0001t0004g0030a0001c0001t0004g0040a0001c0001t0004g0042 | 3 | HG00438.hp1 HG02273.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.34+3973_34+3974ins others(11): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494274 | ||||||
| chr20:33494274
|
T | TATATATA others(6): Show |
2 | a0001c0001t0004g0038a0001c0001t0004g0050 | 2 | HG01070.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.34+3973_34+3974ins others(13): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494274 | ||||||
| chr20:33494274
|
T | TATATATA others(8): Show |
2 | a0001c0001t0004g0039a0001c0001t0004g0054 | 2 | HG01496.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.34+3973_34+3974ins others(15): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494274 | ||||||
| chr20:33494274
|
T | TATATATA others(10): Show |
2 | a0001c0001t0004g0037a0001c0001t0004g0048 | 2 | HG01952.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.34+3973_34+3974ins others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494274 | ||||||
| chr20:33494274
|
T | TATATATA others(12): Show |
1 | a0001c0001t0004g0049 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.34+3973_34+3974ins others(19): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494274 | ||||||
| chr20:33494275
|
T | A | 8 | a0001c0001t0004g0056a0001c0001t0004g0061a0001c0001t0005g0133others(5): Show | 8 | HG01167.hp2 HG01361.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.34+3974T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494275 | ||||||
| chr20:33494276
|
T | A | 11 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(8): Show | 11 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.34+3975T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494276 | ||||||
| chr20:33494277
|
T | A | 2 | a0001c0001t0004g0056a0001c0001t0004g0061 | 2 | HG02738.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.34+3976T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494277 | ||||||
| chr20:33494278
|
T | A | 10 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(7): Show | 10 | HG01070.hp2 HG01496.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.34+3977T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494278 | ||||||
| chr20:33494280
|
T | A | 5 | a0001c0001t0004g0038a0001c0001t0004g0040a0001c0001t0004g0048others(2): Show | 5 | HG01070.hp2 HG01981.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.34+3979T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494280 | ||||||
| chr20:33494351
|
A | G | 290 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.34+4050A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494351 | ||||||
| chr20:33494374
|
T | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+4073T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494374 | ||||||
| chr20:33494426
|
T | C | 295 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.34+4125T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494426 | ||||||
| chr20:33494571
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+4270G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494571 | ||||||
| chr20:33494610
|
T | A | 1 | a0001c0001t0001g0250 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.34+4309T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494610 | ||||||
| chr20:33494946
|
G | C | 3 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0028 | 3 | HG02615.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.34+4645G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494946 | ||||||
| chr20:33494978
|
T | G | 2 | a0001c0001t0003g0110a0001c0001t0003g0134 | 2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.34+4677T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33494978 | ||||||
| chr20:33495070
|
A | C | 239 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.34+4769A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33495070 | ||||||
| chr20:33495156
|
G | A | 9 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0251others(6): Show | 9 | HG00735.hp2 HG01243.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.34+4855G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33495156 | ||||||
| chr20:33495257
|
C | T | 1 | a0001c0002t0002g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.34+4956C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33495257 | ||||||
| chr20:33495287
|
G | A | 1 | a0001c0002t0002g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.34+4986G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33495287 | ||||||
| chr20:33495291
|
C | T | 1 | a0001c0001t0026g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.34+4990C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33495291 | ||||||
| chr20:33495386
|
C | CA | 34 | a0001c0001t0001g0237a0001c0001t0004g0056a0001c0001t0006g0083others(31): Show | 34 | HG00408.hp2 HG00544.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.34+5104dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33495386 | |||||
| chr20:33495386
|
CAAAAAAA | C | 8 | a0001c0001t0005g0079a0001c0001t0005g0080a0001c0001t0005g0081others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.34+5098_34+5104del others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33495386 | |||||
| chr20:33495396
|
A | G | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.34+5095A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33495396 | ||||||
| chr20:33495838
|
A | G | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+5537A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33495838 | ||||||
| chr20:33495841
|
T | G | 3 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022 | 3 | HG00738.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.34+5540T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33495841 | ||||||
| chr20:33495898
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.34+5597G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33495898 | ||||||
| chr20:33495905
|
A | G | 67 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(64): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.34+5604A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33495905 | ||||||
| chr20:33496412
|
C | T | 1 | a0001c0001t0003g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.34+6111C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33496412 | ||||||
| chr20:33496667
|
G | T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+6366G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33496667 | ||||||
| chr20:33496692
|
TC | T | 7 | a0001c0001t0003g0101a0001c0001t0003g0104a0001c0001t0003g0105others(4): Show | 7 | HG00408.hp1 HG02080.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.34+6394delC | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33496692 | |||||
| chr20:33496739
|
G | A | 3 | a0001c0001t0005g0079a0001c0001t0005g0133a0001c0001t0005g0138 | 3 | HG02145.hp1 HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.34+6438G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33496739 | ||||||
| chr20:33496920
|
C | T | 1 | a0001c0002t0002g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.34+6619C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33496920 | ||||||
| chr20:33497197
|
C | T | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.34+6896C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33497197 | ||||||
| chr20:33497261
|
G | A | 16 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(13): Show | 16 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+6960G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33497261 | ||||||
| chr20:33497274
|
C | CA | 71 | a0001c0001t0001g0222a0001c0001t0001g0234a0001c0001t0001g0269others(68): Show | 71 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.34+6997dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33497274 | |||||
| chr20:33497274
|
C | CAA | 79 | a0001c0001t0001g0238a0001c0001t0003g0071a0001c0001t0003g0072others(76): Show | 79 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.34+6996_34+6997dup others(2): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33497274 | |||||
| chr20:33497274
|
C | CAAA | 26 | a0001c0001t0003g0090a0001c0001t0003g0104a0001c0001t0003g0106others(23): Show | 26 | HG00408.hp1 HG01361.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.34+6995_34+6997dup others(3): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33497274 | |||||
| chr20:33497274
|
CA | C | 15 | a0001c0001t0001g0220a0001c0001t0001g0239a0001c0001t0001g0247others(12): Show | 15 | HG01255.hp1 HG01261.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.34+6997delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33497274 | |||||
| chr20:33497274
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+6987_34+6997del others(11): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33497274 | |||||
| chr20:33497362
|
T | C | 285 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(282): Show | 285 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.34+7061T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33497362 | ||||||
| chr20:33497363
|
G | A | 1 | a0001c0002t0002g0203 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.34+7062G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33497363 | ||||||
| chr20:33497428
|
A | G | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+7127A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33497428 | ||||||
| chr20:33497485
|
T | C | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.34+7184T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33497485 | ||||||
| chr20:33497539
|
C | G | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+7238C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33497539 | ||||||
| chr20:33497547
|
C | CT | 89 | a0001c0001t0001g0250a0001c0001t0001g0277a0001c0001t0001g0298others(86): Show | 89 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.34+7267dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33497547 | |||||
| chr20:33497547
|
C | CTT | 8 | a0001c0001t0003g0149a0001c0001t0005g0146a0001c0001t0006g0143others(5): Show | 8 | HG00438.hp2 HG02135.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.34+7266_34+7267dup others(2): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33497547 | |||||
| chr20:33497547
|
CT | C | 37 | a0001c0001t0001g0225a0001c0001t0004g0017a0001c0001t0004g0019others(34): Show | 37 | HG00738.hp2 HG01070.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.34+7267delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33497547 | |||||
| chr20:33497643
|
G | A | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+7342G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33497643 | ||||||
| chr20:33497830
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+7529G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33497830 | ||||||
| chr20:33497895
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+7594C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33497895 | ||||||
| chr20:33498115
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+7814G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33498115 | ||||||
| chr20:33498247
|
CT | C | 8 | a0001c0001t0001g0225a0001c0001t0001g0234a0001c0001t0030g0001others(5): Show | 8 | HG00323.hp1 HG01070.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.34+7962delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33498247 | |||||
| chr20:33498445
|
G | A | 4 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+8144G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33498445 | ||||||
| chr20:33498500
|
A | G | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+8199A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33498500 | ||||||
| chr20:33498607
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.34+8306A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33498607 | ||||||
| chr20:33498641
|
C | T | 87 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(84): Show | 87 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.34+8340C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33498641 | ||||||
| chr20:33498642
|
G | A | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+8341G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33498642 | ||||||
| chr20:33498672
|
C | A | 1 | a0001c0001t0019g0117 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.34+8371C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33498672 | ||||||
| chr20:33498783
|
C | T | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+8482C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33498783 | ||||||
| chr20:33498920
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.34+8619A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33498920 | ||||||
| chr20:33499000
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.34+8699C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33499000 | ||||||
| chr20:33499048
|
G | GA | 76 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(73): Show | 76 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.34+8761dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33499048 | |||||
| chr20:33499048
|
G | GAAA | 12 | a0001c0001t0003g0089a0001c0001t0003g0090a0001c0001t0003g0109others(9): Show | 12 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+8759_34+8761dup others(3): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33499048 | |||||
| chr20:33499048
|
GA | G | 37 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(34): Show | 37 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.34+8761delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33499048 | |||||
| chr20:33499059
|
A | T | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.34+8758A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33499059 | ||||||
| chr20:33499068
|
A | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+8767A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33499068 | ||||||
| chr20:33499180
|
C | T | 4 | a0001c0001t0013g0197a0001c0001t0013g0199a0001c0001t0013g0212others(1): Show | 4 | HG02622.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+8879C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33499180 | ||||||
| chr20:33499195
|
A | G | 291 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.34+8894A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33499195 | ||||||
| chr20:33499555
|
C | G | 10 | a0001c0001t0004g0017a0001c0001t0004g0020a0001c0001t0004g0021others(7): Show | 10 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.34+9254C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33499555 | ||||||
| chr20:33499643
|
G | A | 5 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(2): Show | 5 | HG01070.hp2 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+9342G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33499643 | ||||||
| chr20:33499935
|
G | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+9634G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33499935 | ||||||
| chr20:33499968
|
T | C | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+9667T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33499968 | ||||||
| chr20:33500119
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+9818G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33500119 | ||||||
| chr20:33500286
|
A | G | 4 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0187others(1): Show | 4 | HG00735.hp1 HG01070.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+9985A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33500286 | ||||||
| chr20:33500336
|
G | T | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+10035G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33500336 | ||||||
| chr20:33500396
|
A | G | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+10095A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33500396 | ||||||
| chr20:33500469
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.34+10168G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33500469 | ||||||
| chr20:33500547
|
T | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+10246T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33500547 | ||||||
| chr20:33500559
|
A | G | 5 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016others(2): Show | 5 | HG02559.hp1 HG02630.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+10258A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33500559 | ||||||
| chr20:33500625
|
C | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+10324C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33500625 | ||||||
| chr20:33500791
|
TCAGGGGT others(3): Show |
T | 1 | a0001c0003t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.34+10492_34+10501d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33500791 | |||||
| chr20:33500826
|
A | C | 1 | a0001c0002t0002g0288 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.34+10525A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33500826 | ||||||
| chr20:33500976
|
G | A | 1 | a0001c0002t0002g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.34+10675G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33500976 | ||||||
| chr20:33501177
|
C | A | 237 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.34+10876C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33501177 | ||||||
| chr20:33501334
|
A | T | 4 | a0001c0001t0006g0094a0001c0001t0006g0095a0001c0001t0006g0118others(1): Show | 4 | HG00408.hp2 HG00544.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+11033A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33501334 | ||||||
| chr20:33501406
|
T | A | 10 | a0001c0001t0004g0017a0001c0001t0004g0020a0001c0001t0004g0021others(7): Show | 10 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.34+11105T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33501406 | ||||||
| chr20:33501435
|
A | C | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+11134A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33501435 | ||||||
| chr20:33501625
|
C | T | 2 | a0001c0001t0005g0078a0001c0001t0005g0086 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.34+11324C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33501625 | ||||||
| chr20:33501630
|
C | CT | 32 | a0001c0001t0001g0224a0001c0001t0004g0017a0001c0001t0004g0019others(29): Show | 32 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.34+11357dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33501630 | |||||
| chr20:33501630
|
C | CTT | 101 | a0001c0001t0001g0195a0001c0001t0001g0220a0001c0001t0001g0223others(98): Show | 101 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.34+11356_34+11357d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33501630 | |||||
| chr20:33501630
|
C | CTTT | 46 | a0001c0001t0001g0159a0001c0001t0001g0222a0001c0001t0001g0228others(43): Show | 46 | HG00323.hp2 HG00408.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.34+11355_34+11357d others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33501630 | |||||
| chr20:33501630
|
C | CTTTT | 46 | a0001c0001t0003g0077a0001c0001t0003g0087a0001c0001t0003g0090others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.34+11354_34+11357d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33501630 | |||||
| chr20:33501630
|
C | CTTTTT | 27 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(24): Show | 27 | HG00621.hp1 HG01106.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.34+11353_34+11357d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33501630 | |||||
| chr20:33501630
|
C | CTTTTTT | 8 | a0001c0001t0003g0126a0001c0001t0003g0128a0001c0001t0005g0136others(5): Show | 8 | HG01243.hp2 HG02630.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.34+11352_34+11357d others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33501630 | |||||
| chr20:33501630
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0040g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.34+11348_34+11357d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33501630 | |||||
| chr20:33501630
|
CT | C | 9 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(6): Show | 9 | HG01261.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.34+11357delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33501630 | |||||
| chr20:33501630
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0006g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.34+11347_34+11357d others(13): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33501630 | |||||
| chr20:33501630
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0006g0091a0001c0001t0006g0143a0001c0001t0006g0157 | 3 | HG01361.hp2 HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.34+11345_34+11357d others(15): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33501630 | |||||
| chr20:33501679
|
C | T | 7 | a0001c0001t0005g0078a0001c0001t0005g0084a0001c0001t0005g0085others(4): Show | 7 | HG02647.hp2 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+11378C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33501679 | ||||||
| chr20:33501708
|
C | T | 4 | a0001c0002t0002g0196a0001c0002t0002g0206a0001c0002t0002g0211others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+11407C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33501708 | ||||||
| chr20:33501946
|
C | T | 291 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.34+11645C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33501946 | ||||||
| chr20:33501950
|
A | AT | 291 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.34+11652dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33501950 | |||||
| chr20:33501955
|
C | T | 291 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.34+11654C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33501955 | ||||||
| chr20:33502096
|
G | A | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.34+11795G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33502096 | ||||||
| chr20:33502341
|
T | C | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+12040T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33502341 | ||||||
| chr20:33502469
|
C | G | 87 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(84): Show | 87 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.34+12168C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33502469 | ||||||
| chr20:33502628
|
C | T | 3 | a0001c0001t0003g0096a0001c0001t0003g0145a0001c0001t0003g0153 | 3 | HG02615.hp1 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.34+12327C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33502628 | ||||||
| chr20:33502636
|
C | A | 1 | a0004c0007t0002g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.34+12335C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33502636 | ||||||
| chr20:33502686
|
A | T | 1 | a0001c0001t0004g0051 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.34+12385A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33502686 | ||||||
| chr20:33502839
|
C | G | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+12538C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33502839 | ||||||
| chr20:33503051
|
A | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+12750A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503051 | ||||||
| chr20:33503090
|
C | CA | 11 | a0001c0001t0004g0026a0001c0001t0004g0028a0001c0001t0004g0030others(8): Show | 11 | HG02486.hp2 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.34+12814dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33503090 | |||||
| chr20:33503090
|
CA | C | 80 | a0001c0001t0001g0267a0001c0001t0001g0270a0001c0001t0001g0272others(77): Show | 80 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.34+12814delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33503090 | |||||
| chr20:33503090
|
CAA | C | 157 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.34+12813_34+12814d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33503090 | |||||
| chr20:33503254
|
C | CT | 142 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(139): Show | 142 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.34+12971dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33503254 | |||||
| chr20:33503254
|
CT | C | 58 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(55): Show | 58 | HG00438.hp1 HG00738.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.34+12971delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33503254 | |||||
| chr20:33503255
|
T | TTTC | 18 | a0001c0001t0003g0156a0001c0001t0005g0125a0001c0001t0006g0083others(15): Show | 18 | HG00408.hp2 HG00544.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.34+12956_34+12957i others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33503255 | |||||
| chr20:33503256
|
T | TTC | 56 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(53): Show | 56 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.34+12956_34+12957i others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33503256 | |||||
| chr20:33503257
|
T | TC | 12 | a0001c0001t0003g0089a0001c0001t0003g0109a0001c0001t0003g0110others(9): Show | 12 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+12956_34+12957i others(3): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503257 | ||||||
| chr20:33503258
|
T | C | 1 | a0001c0001t0003g0090 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.34+12957T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503258 | ||||||
| chr20:33503259
|
T | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+12958T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503259 | ||||||
| chr20:33503260
|
T | C | 2 | a0001c0001t0006g0091a0001c0001t0006g0143 | 2 | HG01361.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.34+12959T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503260 | ||||||
| chr20:33503282
|
T | A | 1 | a0002c0008t0002g0047 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.34+12981T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503282 | ||||||
| chr20:33503285
|
C | A | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+12984C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503285 | ||||||
| chr20:33503286
|
G | A | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+12985G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503286 | ||||||
| chr20:33503347
|
C | T | 4 | a0001c0001t0004g0041a0001c0001t0004g0048a0001c0001t0004g0049others(1): Show | 4 | NA18944.hp2 NA18960.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+13046C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503347 | ||||||
| chr20:33503399
|
C | A | 1 | a0001c0001t0001g0274 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.34+13098C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503399 | ||||||
| chr20:33503400
|
G | T | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+13099G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503400 | ||||||
| chr20:33503426
|
T | C | 1 | a0001c0002t0002g0204 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.34+13125T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503426 | ||||||
| chr20:33503432
|
T | C | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.34+13131T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503432 | ||||||
| chr20:33503532
|
C | T | 1 | a0001c0001t0015g0015 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.34+13231C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503532 | ||||||
| chr20:33503543
|
G | A | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+13242G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503543 | ||||||
| chr20:33503627
|
T | C | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+13326T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503627 | ||||||
| chr20:33503633
|
T | G | 1 | a0001c0001t0003g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.34+13332T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503633 | ||||||
| chr20:33503720
|
C | A | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+13419C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503720 | ||||||
| chr20:33503995
|
C | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+13694C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33503995 | ||||||
| chr20:33504034
|
A | G | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+13733A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33504034 | ||||||
| chr20:33504403
|
C | CT | 34 | a0001c0001t0001g0257a0001c0001t0003g0123a0001c0001t0004g0019others(31): Show | 34 | HG00438.hp1 HG00738.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.34+14125dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33504403 | |||||
| chr20:33504403
|
CT | C | 18 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0251others(15): Show | 18 | HG00597.hp2 HG01070.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.34+14125delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33504403 | |||||
| chr20:33504473
|
GCTCACGG others(4): Show |
G | 16 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(13): Show | 16 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+14176_34+14186d others(13): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33504473 | |||||
| chr20:33504700
|
G | A | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+14399G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33504700 | ||||||
| chr20:33504758
|
C | T | 2 | a0001c0001t0003g0105a0001c0001t0003g0107 | 2 | NA18965.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.34+14457C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33504758 | ||||||
| chr20:33504799
|
G | C | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+14498G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33504799 | ||||||
| chr20:33504960
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.34+14659G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33504960 | ||||||
| chr20:33505111
|
G | A | 8 | a0001c0001t0005g0079a0001c0001t0005g0080a0001c0001t0005g0081others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.34+14810G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33505111 | ||||||
| chr20:33505150
|
T | G | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+14849T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33505150 | ||||||
| chr20:33505220
|
A | G | 1 | a0001c0001t0042g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.34+14919A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33505220 | ||||||
| chr20:33505239
|
T | C | 10 | a0001c0001t0004g0017a0001c0001t0004g0020a0001c0001t0004g0021others(7): Show | 10 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.34+14938T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33505239 | ||||||
| chr20:33505431
|
A | G | 4 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+15130A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33505431 | ||||||
| chr20:33505466
|
C | A | 1 | a0001c0001t0004g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.34+15165C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33505466 | ||||||
| chr20:33505608
|
C | T | 1 | a0001c0001t0004g0042 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.34+15307C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33505608 | ||||||
| chr20:33505670
|
G | A | 243 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.34+15369G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33505670 | ||||||
| chr20:33505730
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.34+15429G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33505730 | ||||||
| chr20:33505754
|
C | A | 14 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.34+15453C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33505754 | ||||||
| chr20:33506124
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+15823G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33506124 | ||||||
| chr20:33506137
|
G | T | 1 | a0001c0001t0003g0145 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.34+15836G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33506137 | ||||||
| chr20:33506307
|
A | G | 291 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.34+16006A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33506307 | ||||||
| chr20:33506518
|
G | A | 68 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(65): Show | 68 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.34+16217G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33506518 | ||||||
| chr20:33506527
|
A | G | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+16226A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33506527 | ||||||
| chr20:33506586
|
A | G | 1 | a0001c0001t0010g0088 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.34+16285A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33506586 | ||||||
| chr20:33507144
|
T | C | 2 | a0001c0001t0003g0097a0001c0001t0003g0147 | 2 | HG00597.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.34+16843T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33507144 | ||||||
| chr20:33507169
|
T | C | 1 | a0001c0002t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.34+16868T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33507169 | ||||||
| chr20:33507411
|
G | A | 14 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.34+17110G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33507411 | ||||||
| chr20:33507440
|
G | C | 1 | a0001c0001t0006g0094 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.34+17139G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33507440 | ||||||
| chr20:33507799
|
A | G | 4 | a0001c0001t0003g0126a0001c0001t0003g0128a0001c0001t0003g0129others(1): Show | 4 | HG00621.hp1 NA18941.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+17498A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33507799 | ||||||
| chr20:33507834
|
G | A | 1 | a0001c0001t0037g0296 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.34+17533G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33507834 | ||||||
| chr20:33508121
|
G | A | 1 | a0001c0001t0007g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.34+17820G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33508121 | ||||||
| chr20:33508306
|
G | A | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+18005G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33508306 | ||||||
| chr20:33508473
|
G | T | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+18172G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33508473 | ||||||
| chr20:33508509
|
T | C | 1 | a0001c0002t0002g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.34+18208T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33508509 | ||||||
| chr20:33508625
|
A | G | 1 | a0001c0005t0002g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.34+18324A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33508625 | ||||||
| chr20:33508734
|
C | G | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+18433C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33508734 | ||||||
| chr20:33509072
|
A | T | 1 | a0001c0001t0004g0058 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.34+18771A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33509072 | ||||||
| chr20:33509127
|
A | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+18826A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33509127 | ||||||
| chr20:33509231
|
G | T | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+18930G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33509231 | ||||||
| chr20:33509236
|
A | G | 255 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.34+18935A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33509236 | ||||||
| chr20:33509504
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+19203C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33509504 | ||||||
| chr20:33509822
|
C | CT | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+19536dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33509822 | |||||
| chr20:33509822
|
CT | C | 16 | a0001c0001t0003g0089a0001c0001t0003g0145a0001c0001t0004g0017others(13): Show | 16 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+19536delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33509822 | |||||
| chr20:33510195
|
C | A | 1 | a0001c0001t0007g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.34+19894C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33510195 | ||||||
| chr20:33510425
|
A | G | 1 | a0001c0001t0001g0298 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.34+20124A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33510425 | ||||||
| chr20:33510457
|
C | T | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+20156C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33510457 | ||||||
| chr20:33510502
|
C | T | 1 | a0001c0001t0042g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.34+20201C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33510502 | ||||||
| chr20:33510559
|
G | A | 4 | a0001c0001t0013g0197a0001c0001t0013g0199a0001c0001t0013g0212others(1): Show | 4 | HG02622.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+20258G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33510559 | ||||||
| chr20:33510770
|
T | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+20469T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33510770 | ||||||
| chr20:33510892
|
A | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+20591A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33510892 | ||||||
| chr20:33511173
|
C | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+20872C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33511173 | ||||||
| chr20:33511215
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.34+20914C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33511215 | ||||||
| chr20:33511352
|
A | G | 1 | a0001c0002t0002g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.34+21051A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33511352 | ||||||
| chr20:33511445
|
T | C | 1 | a0001c0002t0002g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.34+21144T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33511445 | ||||||
| chr20:33511546
|
A | G | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+21245A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33511546 | ||||||
| chr20:33511752
|
T | TGCATGCC others(152): Show |
1 | a0001c0001t0003g0126 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.34+21452_34+21610d others(161): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33511752 | |||||
| chr20:33511921
|
T | A | 2 | a0001c0001t0004g0029a0001c0001t0004g0030 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.34+21620T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33511921 | ||||||
| chr20:33511935
|
T | C | 1 | a0001c0001t0003g0111 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.34+21634T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33511935 | ||||||
| chr20:33512038
|
G | A | 2 | a0001c0001t0019g0082a0001c0001t0019g0117 | 2 | NA18971.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.34+21737G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33512038 | ||||||
| chr20:33512106
|
G | A | 4 | a0001c0001t0004g0041a0001c0001t0004g0048a0001c0001t0004g0049others(1): Show | 4 | NA18944.hp2 NA18960.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+21805G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33512106 | ||||||
| chr20:33512106
|
G | C | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+21805G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33512106 | ||||||
| chr20:33512216
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.34+21915G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33512216 | ||||||
| chr20:33512244
|
G | A | 1 | a0001c0002t0002g0210 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.34+21943G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33512244 | ||||||
| chr20:33512273
|
C | T | 2 | a0001c0001t0005g0130a0001c0001t0005g0155 | 2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.34+21972C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33512273 | ||||||
| chr20:33512458
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.34+22157C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33512458 | ||||||
| chr20:33512740
|
G | A | 2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.34+22439G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33512740 | ||||||
| chr20:33512750
|
C | CT | 15 | a0001c0001t0001g0267a0001c0001t0001g0298a0001c0001t0004g0026others(12): Show | 15 | HG01074.hp1 HG01175.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.34+22466dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33512750 | |||||
| chr20:33512838
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.34+22537C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33512838 | ||||||
| chr20:33513178
|
A | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+22877A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33513178 | ||||||
| chr20:33513354
|
T | G | 237 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.34+23053T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33513354 | ||||||
| chr20:33513355
|
T | G | 16 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0080others(13): Show | 16 | HG01243.hp2 HG02145.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.34+23054T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33513355 | ||||||
| chr20:33513578
|
G | T | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+23277G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33513578 | ||||||
| chr20:33513610
|
G | C | 297 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.34+23309G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33513610 | ||||||
| chr20:33513683
|
A | G | 290 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.34+23382A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33513683 | ||||||
| chr20:33513816
|
G | GA | 229 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.34+23535dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33513816 | |||||
| chr20:33513905
|
TTTG | T | 4 | a0001c0001t0001g0245a0001c0002t0002g0196a0001c0002t0002g0206others(1): Show | 4 | HG01891.hp1 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+23619_34+23621d others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33513905 | |||||
| chr20:33514151
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+23850C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33514151 | ||||||
| chr20:33514206
|
G | GT | 97 | a0001c0001t0001g0225a0001c0001t0001g0237a0001c0001t0001g0240others(94): Show | 97 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.34+23931dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33514206 | |||||
| chr20:33514206
|
G | GTT | 88 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(85): Show | 88 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.34+23930_34+23931d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33514206 | |||||
| chr20:33514206
|
G | GTTT | 6 | a0001c0001t0001g0261a0001c0001t0001g0280a0001c0001t0003g0109others(3): Show | 6 | HG01261.hp1 HG02257.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.34+23929_34+23931d others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33514206 | |||||
| chr20:33514206
|
GT | G | 7 | a0001c0001t0004g0017a0001c0001t0004g0051a0001c0001t0004g0054others(4): Show | 7 | HG01167.hp2 HG01981.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.34+23931delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33514206 | |||||
| chr20:33514206
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0277 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.34+23920_34+23931d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33514206 | |||||
| chr20:33514216
|
T | G | 4 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0006t0007g0282others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+23915T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33514216 | ||||||
| chr20:33514271
|
GTGGTGCG others(12): Show |
G | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+23972_34+23990d others(21): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33514271 | |||||
| chr20:33514277
|
C | T | 1 | a0001c0001t0004g0026 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.34+23976C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33514277 | ||||||
| chr20:33514526
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.34+24225A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33514526 | ||||||
| chr20:33514526
|
A | T | 2 | a0001c0001t0004g0029a0001c0001t0004g0030 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.34+24225A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33514526 | ||||||
| chr20:33514528
|
G | C | 2 | a0001c0001t0004g0029a0001c0001t0004g0030 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.34+24227G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33514528 | ||||||
| chr20:33514651
|
T | C | 1 | a0001c0001t0003g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.34+24350T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33514651 | ||||||
| chr20:33514813
|
C | T | 1 | a0001c0001t0008g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.34+24512C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33514813 | ||||||
| chr20:33514935
|
G | A | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+24634G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33514935 | ||||||
| chr20:33514938
|
C | T | 1 | a0001c0001t0008g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.34+24637C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33514938 | ||||||
| chr20:33515071
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+24770G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33515071 | ||||||
| chr20:33515162
|
A | G | 5 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016others(2): Show | 5 | HG02559.hp1 HG02630.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+24861A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33515162 | ||||||
| chr20:33515169
|
G | A | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.34+24868G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33515169 | ||||||
| chr20:33515224
|
G | T | 3 | a0001c0001t0006g0091a0001c0001t0006g0143a0001c0001t0006g0157 | 3 | HG01361.hp2 HG02698.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.34+24923G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33515224 | ||||||
| chr20:33515278
|
G | T | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.34+24977G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33515278 | ||||||
| chr20:33515350
|
C | CA | 241 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.34+25070dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33515350 | |||||
| chr20:33515350
|
C | CAA | 10 | a0001c0001t0005g0133a0001c0001t0005g0155a0001c0001t0006g0091others(7): Show | 10 | HG01175.hp1 HG01361.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.34+25069_34+25070d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33515350 | |||||
| chr20:33515350
|
CAAAAAAA | C | 29 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(26): Show | 29 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.34+25064_34+25070d others(9): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33515350 | |||||
| chr20:33515464
|
A | G | 1 | a0001c0001t0003g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.34+25163A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33515464 | ||||||
| chr20:33515486
|
T | G | 1 | a0001c0005t0002g0179 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.34+25185T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33515486 | ||||||
| chr20:33515709
|
G | C | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.34+25408G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33515709 | ||||||
| chr20:33515717
|
C | A | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+25416C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33515717 | ||||||
| chr20:33515801
|
C | CA | 21 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(18): Show | 21 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.34+25520dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33515801 | |||||
| chr20:33515801
|
CA | C | 215 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.34+25520delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33515801 | |||||
| chr20:33515815
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.34+25514A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33515815 | ||||||
| chr20:33515828
|
G | A | 32 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(29): Show | 32 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.34+25527G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33515828 | ||||||
| chr20:33516057
|
C | G | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+25756C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33516057 | ||||||
| chr20:33516144
|
A | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+25843A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33516144 | ||||||
| chr20:33516197
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.34+25896T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33516197 | ||||||
| chr20:33516842
|
C | T | 30 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(27): Show | 30 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.34+26541C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33516842 | ||||||
| chr20:33517034
|
T | A | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+26733T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33517034 | ||||||
| chr20:33517274
|
G | A | 1 | a0001c0001t0003g0100 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.34+26973G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33517274 | ||||||
| chr20:33517450
|
G | GT | 21 | a0001c0001t0001g0244a0001c0001t0001g0251a0001c0001t0001g0254others(18): Show | 21 | HG00735.hp1 HG00735.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.34+27150dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33517450 | |||||
| chr20:33517452
|
G | GT | 40 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(37): Show | 40 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.34+27166dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33517452 | |||||
| chr20:33517452
|
G | T | 243 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.34+27151G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33517452 | ||||||
| chr20:33517637
|
A | G | 255 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.34+27336A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33517637 | ||||||
| chr20:33517660
|
C | T | 1 | a0001c0001t0004g0040 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.34+27359C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33517660 | ||||||
| chr20:33517689
|
CT | C | 250 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0222others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.34+27403delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33517689 | |||||
| chr20:33517715
|
A | T | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+27414A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33517715 | ||||||
| chr20:33517738
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+27437C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33517738 | ||||||
| chr20:33517805
|
T | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+27504T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33517805 | ||||||
| chr20:33517957
|
T | C | 1 | a0001c0002t0002g0214 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.34+27656T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33517957 | ||||||
| chr20:33518173
|
C | T | 16 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(13): Show | 16 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+27872C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33518173 | ||||||
| chr20:33518177
|
T | C | 16 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0080others(13): Show | 16 | HG01243.hp2 HG02145.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.34+27876T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33518177 | ||||||
| chr20:33518191
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+27890G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33518191 | ||||||
| chr20:33518249
|
C | T | 1 | a0001c0001t0010g0114 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.34+27948C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33518249 | ||||||
| chr20:33518307
|
G | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+28006G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33518307 | ||||||
| chr20:33518606
|
C | CA | 29 | a0001c0001t0003g0108a0001c0001t0003g0147a0001c0001t0004g0017others(26): Show | 29 | HG00738.hp2 HG01074.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.34+28321dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33518606 | |||||
| chr20:33518609
|
A | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+28308A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33518609 | ||||||
| chr20:33518643
|
A | T | 1 | a0001c0002t0002g0289 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.34+28342A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33518643 | ||||||
| chr20:33518703
|
C | G | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+28402C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33518703 | ||||||
| chr20:33518844
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+28543C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33518844 | ||||||
| chr20:33519156
|
C | A | 290 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.34+28855C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33519156 | ||||||
| chr20:33519283
|
G | T | 4 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+28982G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33519283 | ||||||
| chr20:33519466
|
T | C | 78 | a0001c0001t0013g0197a0001c0001t0013g0199a0001c0001t0013g0212others(75): Show | 78 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.34+29165T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33519466 | ||||||
| chr20:33519545
|
C | T | 30 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(27): Show | 30 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.34+29244C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33519545 | ||||||
| chr20:33519546
|
G | A | 1 | a0001c0002t0002g0187 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.34+29245G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33519546 | ||||||
| chr20:33519734
|
A | T | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.34+29433A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33519734 | ||||||
| chr20:33519986
|
A | C | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+29685A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33519986 | ||||||
| chr20:33520027
|
C | T | 239 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.34+29726C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33520027 | ||||||
| chr20:33520227
|
G | C | 1 | a0001c0005t0002g0179 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.34+29926G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33520227 | ||||||
| chr20:33520381
|
T | C | 1 | a0001c0001t0007g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.34+30080T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33520381 | ||||||
| chr20:33520889
|
ACT | A | 3 | a0001c0001t0005g0079a0001c0001t0005g0133a0001c0001t0005g0138 | 3 | HG02145.hp1 HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.34+30589_34+30590d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33520889 | ||||||
| chr20:33520909
|
C | T | 1 | a0001c0002t0002g0205 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.34+30608C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33520909 | ||||||
| chr20:33520970
|
T | TCA | 32 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0255others(29): Show | 32 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.34+30698_34+30699d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33520970 | |||||
| chr20:33520970
|
T | TCACA | 16 | a0001c0001t0004g0026a0001c0001t0004g0029a0001c0001t0004g0030others(13): Show | 16 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+30696_34+30699d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33520970 | |||||
| chr20:33520970
|
TCA | T | 4 | a0001c0001t0014g0293a0001c0001t0037g0296a0001c0001t0040g0295others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+30698_34+30699d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33520970 | |||||
| chr20:33520970
|
TCACA | T | 13 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(10): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.34+30696_34+30699d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33520970 | |||||
| chr20:33520970
|
TCACACAC others(3): Show |
T | 1 | a0001c0001t0010g0114 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.34+30690_34+30699d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33520970 | |||||
| chr20:33521104
|
TTTAGGGG others(8): Show |
T | 1 | a0001c0001t0003g0145 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.34+30804_34+30818d others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521104 | ||||||
| chr20:33521108
|
G | A | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.34+30807G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521108 | ||||||
| chr20:33521139
|
G | A | 2 | a0001c0001t0010g0088a0001c0001t0022g0103 | 2 | NA18969.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.34+30838G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521139 | ||||||
| chr20:33521181
|
A | G | 4 | a0001c0001t0013g0197a0001c0001t0013g0199a0001c0001t0013g0212others(1): Show | 4 | HG02622.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+30880A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521181 | ||||||
| chr20:33521344
|
A | G | 1 | a0001c0002t0002g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.34+31043A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521344 | ||||||
| chr20:33521409
|
A | G | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+31108A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521409 | ||||||
| chr20:33521535
|
T | C | 1 | a0001c0005t0002g0179 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.34+31234T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521535 | ||||||
| chr20:33521562
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+31261G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521562 | ||||||
| chr20:33521645
|
G | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+31344G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521645 | ||||||
| chr20:33521733
|
C | A | 239 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.34+31432C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521733 | ||||||
| chr20:33521797
|
A | C | 1 | a0001c0001t0004g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.34+31496A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521797 | ||||||
| chr20:33521799
|
A | G | 1 | a0001c0001t0003g0148 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.34+31498A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521799 | ||||||
| chr20:33521823
|
C | CGT | 39 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(36): Show | 39 | HG00408.hp2 HG00544.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.34+31545_34+31546d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33521823 | |||||
| chr20:33521823
|
C | CGTGT | 3 | a0001c0001t0015g0016a0001c0001t0037g0296a0001c0001t0040g0295 | 3 | HG02109.hp2 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.34+31543_34+31546d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33521823 | |||||
| chr20:33521909
|
T | C | 2 | a0001c0001t0005g0136a0001c0001t0039g0137 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.34+31608T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33521909 | ||||||
| chr20:33522243
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+31942G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33522243 | ||||||
| chr20:33522334
|
A | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+32033A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33522334 | ||||||
| chr20:33522336
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.34+32035A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33522336 | ||||||
| chr20:33522339
|
T | TAACAGAG others(50): Show |
16 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(13): Show | 16 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+32039_34+32095d others(59): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33522339 | |||||
| chr20:33522398
|
T | C | 78 | a0001c0001t0013g0197a0001c0001t0013g0199a0001c0001t0013g0212others(75): Show | 78 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.34+32097T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33522398 | ||||||
| chr20:33522506
|
T | C | 87 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(84): Show | 87 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.34+32205T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33522506 | ||||||
| chr20:33522564
|
T | A | 1 | a0001c0001t0003g0111 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.34+32263T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33522564 | ||||||
| chr20:33522982
|
C | T | 243 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.34+32681C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33522982 | ||||||
| chr20:33523075
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+32774C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33523075 | ||||||
| chr20:33523722
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.34+33421C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33523722 | ||||||
| chr20:33523778
|
T | G | 2 | a0001c0001t0030g0001a0001c0010t0028g0132 | 2 | HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+33477T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33523778 | ||||||
| chr20:33524062
|
T | G | 3 | a0001c0002t0002g0196a0001c0002t0002g0206a0001c0002t0002g0211 | 3 | HG01891.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.34+33761T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33524062 | ||||||
| chr20:33524091
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.34+33790G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33524091 | ||||||
| chr20:33524092
|
T | G | 239 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.34+33791T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33524092 | ||||||
| chr20:33524274
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+33973C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33524274 | ||||||
| chr20:33524443
|
T | A | 1 | a0001c0002t0027g0213 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.34+34142T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33524443 | ||||||
| chr20:33524502
|
G | A | 1 | a0001c0001t0004g0040 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.34+34201G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33524502 | ||||||
| chr20:33524547
|
C | A | 3 | a0001c0002t0002g0196a0001c0002t0002g0206a0001c0002t0002g0211 | 3 | HG01891.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.34+34246C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33524547 | ||||||
| chr20:33524603
|
TA | T | 5 | a0001c0001t0001g0261a0001c0001t0001g0280a0001c0001t0004g0019others(2): Show | 5 | HG03195.hp2 NA18960.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+34312delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33524603 | |||||
| chr20:33525131
|
C | T | 239 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.34+34830C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33525131 | ||||||
| chr20:33525187
|
A | AT | 36 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0023others(33): Show | 36 | HG00438.hp1 HG01070.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.34+34901dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33525187 | |||||
| chr20:33525242
|
A | G | 1 | a0001c0001t0004g0026 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.34+34941A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33525242 | ||||||
| chr20:33525587
|
C | T | 1 | a0001c0002t0002g0167 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.34+35286C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33525587 | ||||||
| chr20:33525737
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+35436G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33525737 | ||||||
| chr20:33525880
|
C | T | 1 | a0001c0002t0002g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.34+35579C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33525880 | ||||||
| chr20:33525956
|
G | A | 2 | a0001c0002t0002g0183a0001c0002t0002g0201 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.34+35655G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33525956 | ||||||
| chr20:33526177
|
G | A | 3 | a0001c0001t0021g0265a0001c0001t0021g0278a0001c0001t0043g0221 | 3 | HG02735.hp1 HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.34+35876G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526177 | ||||||
| chr20:33526220
|
A | T | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+35919A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526220 | ||||||
| chr20:33526324
|
G | C | 1 | a0002c0008t0002g0047 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.34+36023G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526324 | ||||||
| chr20:33526441
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+36140A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526441 | ||||||
| chr20:33526522
|
T | G | 1 | a0001c0002t0002g0059 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.34+36221T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526522 | ||||||
| chr20:33526555
|
T | A | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.34+36254T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526555 | ||||||
| chr20:33526582
|
C | T | 1 | a0001c0005t0002g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.34+36281C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526582 | ||||||
| chr20:33526589
|
C | T | 6 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0235others(3): Show | 6 | HG00597.hp1 HG01175.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.34+36288C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526589 | ||||||
| chr20:33526704
|
A | G | 1 | a0001c0001t0006g0095 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.34+36403A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526704 | ||||||
| chr20:33526720
|
G | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+36419G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526720 | ||||||
| chr20:33526724
|
A | C | 7 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.34+36423A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526724 | ||||||
| chr20:33526730
|
CA | C | 95 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(92): Show | 95 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.34+36440delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33526730 | |||||
| chr20:33526918
|
G | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+36617G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526918 | ||||||
| chr20:33526977
|
G | T | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+36676G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526977 | ||||||
| chr20:33526978
|
G | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+36677G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33526978 | ||||||
| chr20:33527091
|
T | C | 255 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.34+36790T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527091 | ||||||
| chr20:33527227
|
A | G | 1 | a0001c0002t0016g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.34+36926A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527227 | ||||||
| chr20:33527294
|
C | T | 74 | a0001c0001t0014g0032a0001c0001t0033g0052a0001c0002t0002g0031others(71): Show | 74 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.34+36993C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527294 | ||||||
| chr20:33527368
|
AT | A | 228 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(225): Show | 228 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.34+37089delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33527368 | |||||
| chr20:33527368
|
ATT | A | 20 | a0001c0001t0001g0259a0001c0001t0001g0261a0001c0001t0003g0145others(17): Show | 20 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.34+37088_34+37089d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33527368 | |||||
| chr20:33527520
|
G | A | 16 | a0001c0001t0006g0083a0001c0001t0006g0091a0001c0001t0006g0094others(13): Show | 16 | HG00408.hp2 HG00544.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.34+37219G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527520 | ||||||
| chr20:33527569
|
C | T | 1 | a0001c0001t0007g0067 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.34+37268C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527569 | ||||||
| chr20:33527583
|
G | A | 10 | a0001c0003t0001g0226a0001c0003t0001g0227a0001c0003t0001g0229others(7): Show | 10 | NA18941.hp1 NA18968.hp1 NA18982.hp2 others(7): Show |
intron_variant | MODIFIER | c.34+37282G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527583 | ||||||
| chr20:33527630
|
C | T | 30 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(27): Show | 30 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.34+37329C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527630 | ||||||
| chr20:33527667
|
C | G | 8 | a0001c0001t0005g0079a0001c0001t0005g0080a0001c0001t0005g0081others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.34+37366C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527667 | ||||||
| chr20:33527707
|
T | C | 2 | a0001c0001t0003g0131a0001c0001t0020g0160 | 2 | HG00558.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.34+37406T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527707 | ||||||
| chr20:33527710
|
T | TG | 3 | a0001c0001t0015g0015a0001c0001t0031g0068a0001c0001t0032g0070 | 3 | HG02630.hp2 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.34+37409_34+37410i others(3): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527710 | ||||||
| chr20:33527712
|
T | G | 1 | a0001c0001t0026g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.34+37411T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527712 | ||||||
| chr20:33527736
|
G | A | 1 | a0001c0002t0002g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.34+37435G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527736 | ||||||
| chr20:33527759
|
G | A | 1 | a0001c0001t0003g0090 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.34+37458G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33527759 | ||||||
| chr20:33528174
|
G | A | 1 | a0001c0002t0002g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.34+37873G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33528174 | ||||||
| chr20:33528241
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0255 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.34+37940G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33528241 | ||||||
| chr20:33528540
|
C | A | 68 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(65): Show | 68 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.34+38239C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33528540 | ||||||
| chr20:33528691
|
CGT | C | 288 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.34+38408_34+38409d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33528691 | |||||
| chr20:33528834
|
C | T | 19 | a0001c0001t0001g0220a0001c0001t0001g0228a0001c0001t0001g0234others(16): Show | 19 | HG00597.hp1 HG00621.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.34+38533C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33528834 | ||||||
| chr20:33529010
|
AGTTTGTT others(10): Show |
A | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.34+38726_34+38742d others(19): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529010 | |||||
| chr20:33529049
|
G | A | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+38748G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529049 | ||||||
| chr20:33529087
|
G | T | 1 | a0001c0001t0001g0224 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.34+38786G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529087 | ||||||
| chr20:33529359
|
A | G | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+39058A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529359 | ||||||
| chr20:33529372
|
C | G | 1 | a0001c0001t0003g0111 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.34+39071C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529372 | ||||||
| chr20:33529415
|
C | T | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+39114C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529415 | ||||||
| chr20:33529742
|
G | GTT | 6 | a0001c0001t0004g0037a0001c0001t0004g0040a0001c0001t0004g0042others(3): Show | 6 | HG00438.hp1 HG01952.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.34+39442_34+39443d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529742 | |||||
| chr20:33529743
|
T | TTTTA | 5 | a0001c0001t0004g0041a0001c0001t0004g0048a0001c0001t0004g0049others(2): Show | 5 | HG02809.hp2 NA18944.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.34+39443_34+39444i others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
T | TTTTATAT others(1): Show |
4 | a0001c0001t0004g0038a0001c0001t0004g0058a0001c0001t0007g0010others(1): Show | 4 | HG01070.hp2 HG02155.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+39443_34+39444i others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
T | TTTTATAT others(3): Show |
4 | a0001c0001t0004g0039a0001c0001t0007g0008a0001c0001t0007g0013others(1): Show | 4 | HG01496.hp1 HG02145.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+39443_34+39444i others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
T | TTTTATAT others(5): Show |
2 | a0001c0001t0008g0004a0001c0001t0008g0007 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.34+39443_34+39444i others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
T | TTTTATAT others(7): Show |
1 | a0001c0001t0007g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.34+39443_34+39444i others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
T | TTTTATAT others(13): Show |
2 | a0001c0001t0008g0002a0001c0001t0008g0006 | 2 | HG01261.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.34+39443_34+39444i others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
TTA | T | 5 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+39480_34+39481d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
TTATA | T | 7 | a0001c0001t0004g0017a0001c0001t0007g0067a0001c0001t0007g0069others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+39478_34+39481d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
TTATATA | T | 5 | a0001c0001t0012g0162a0001c0001t0012g0164a0001c0001t0015g0015others(2): Show | 5 | HG01167.hp2 NA18522.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+39476_34+39481d others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
TTATATAT others(1): Show |
T | 14 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.34+39474_34+39481d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
TTATATAT others(3): Show |
T | 14 | a0001c0001t0003g0105a0001c0001t0003g0109a0001c0001t0003g0113others(11): Show | 14 | HG00741.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.34+39472_34+39481d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
TTATATAT others(5): Show |
T | 168 | a0001c0001t0001g0220a0001c0001t0001g0228a0001c0001t0001g0234others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.34+39470_34+39481d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
TTATATAT others(7): Show |
T | 53 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0222others(50): Show | 53 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.34+39468_34+39481d others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529743
|
TTATATAT others(15): Show |
T | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+39460_34+39481d others(24): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529743 | |||||
| chr20:33529745
|
A | T | 3 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0041g0273 | 3 | HG01261.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.34+39444A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529745 | ||||||
| chr20:33529747
|
A | T | 5 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+39446A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529747 | ||||||
| chr20:33529749
|
A | T | 5 | a0001c0001t0004g0017a0001c0001t0012g0163a0001c0001t0012g0165others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.34+39448A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529749 | ||||||
| chr20:33529751
|
A | T | 5 | a0001c0001t0012g0162a0001c0001t0012g0164a0001c0001t0015g0015others(2): Show | 5 | HG01167.hp2 NA18522.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+39450A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529751 | ||||||
| chr20:33529753
|
A | T | 14 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.34+39452A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529753 | ||||||
| chr20:33529755
|
A | T | 14 | a0001c0001t0003g0105a0001c0001t0003g0109a0001c0001t0003g0113others(11): Show | 14 | HG00741.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.34+39454A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529755 | ||||||
| chr20:33529757
|
A | T | 168 | a0001c0001t0001g0220a0001c0001t0001g0228a0001c0001t0001g0234others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.34+39456A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529757 | ||||||
| chr20:33529759
|
A | T | 53 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0222others(50): Show | 53 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.34+39458A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529759 | ||||||
| chr20:33529767
|
A | T | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+39466A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529767 | ||||||
| chr20:33529771
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0041g0273 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.34+39472_34+39483d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529771 | |||||
| chr20:33529785
|
CT | C | 16 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(13): Show | 16 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+39497delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33529785 | |||||
| chr20:33529951
|
A | T | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+39650A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33529951 | ||||||
| chr20:33530132
|
C | T | 1 | a0001c0001t0004g0058 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.34+39831C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33530132 | ||||||
| chr20:33530206
|
T | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+39905T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33530206 | ||||||
| chr20:33530368
|
G | T | 13 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(10): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.34+40067G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33530368 | ||||||
| chr20:33530422
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.34+40121T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33530422 | ||||||
| chr20:33530611
|
T | C | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.34+40310T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33530611 | ||||||
| chr20:33530794
|
G | C | 2 | a0001c0002t0002g0189a0001c0002t0002g0208 | 2 | HG00741.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.34+40493G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33530794 | ||||||
| chr20:33530795
|
A | G | 1 | a0001c0001t0001g0257 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.34+40494A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33530795 | ||||||
| chr20:33530807
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+40506G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33530807 | ||||||
| chr20:33530816
|
C | A | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+40515C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33530816 | ||||||
| chr20:33530852
|
G | A | 239 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.34+40551G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33530852 | ||||||
| chr20:33530974
|
A | G | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.34+40673A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33530974 | ||||||
| chr20:33531015
|
G | A | 1 | a0001c0001t0004g0017 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.34+40714G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33531015 | ||||||
| chr20:33531078
|
G | A | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+40777G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33531078 | ||||||
| chr20:33531091
|
TAAAC | T | 3 | a0001c0001t0006g0157a0001c0001t0031g0068a0001c0001t0032g0070 | 3 | HG02630.hp2 HG02698.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+40805_34+40808d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33531091 | |||||
| chr20:33531200
|
T | C | 16 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(13): Show | 16 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+40899T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33531200 | ||||||
| chr20:33531362
|
G | C | 1 | a0001c0002t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.34+41061G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33531362 | ||||||
| chr20:33531399
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.34+41098T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33531399 | ||||||
| chr20:33531447
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.34+41146T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33531447 | ||||||
| chr20:33531571
|
A | G | 58 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(55): Show | 58 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.34+41270A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33531571 | ||||||
| chr20:33531732
|
A | G | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+41431A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33531732 | ||||||
| chr20:33531891
|
A | G | 1 | a0001c0001t0004g0024 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.34+41590A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33531891 | ||||||
| chr20:33532169
|
C | T | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+41868C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33532169 | ||||||
| chr20:33532179
|
T | A | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+41878T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33532179 | ||||||
| chr20:33532236
|
C | T | 5 | a0001c0001t0003g0101a0001c0001t0003g0104a0001c0001t0003g0106others(2): Show | 5 | HG00408.hp1 HG02080.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.34+41935C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33532236 | ||||||
| chr20:33532253
|
A | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+41952A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33532253 | ||||||
| chr20:33532364
|
G | A | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+42063G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33532364 | ||||||
| chr20:33532403
|
C | T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+42102C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33532403 | ||||||
| chr20:33532724
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+42423G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33532724 | ||||||
| chr20:33533076
|
C | G | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+42775C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33533076 | ||||||
| chr20:33533118
|
T | TA | 9 | a0001c0001t0005g0078a0001c0001t0005g0084a0001c0001t0005g0085others(6): Show | 9 | HG02647.hp2 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.34+42827dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33533118 | |||||
| chr20:33533272
|
G | A | 1 | a0001c0001t0006g0095 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.34+42971G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33533272 | ||||||
| chr20:33533402
|
A | G | 1 | a0001c0001t0040g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.34+43101A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33533402 | ||||||
| chr20:33533432
|
C | T | 4 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+43131C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33533432 | ||||||
| chr20:33533585
|
C | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+43284C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33533585 | ||||||
| chr20:33533671
|
A | T | 4 | a0001c0001t0003g0077a0001c0001t0003g0135a0001c0001t0014g0184others(1): Show | 4 | HG01346.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+43370A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33533671 | ||||||
| chr20:33533696
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0042g0194 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.34+43395G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33533696 | ||||||
| chr20:33533715
|
T | G | 1 | a0001c0001t0001g0270 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.34+43414T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33533715 | ||||||
| chr20:33533881
|
T | C | 68 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(65): Show | 68 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.34+43580T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33533881 | ||||||
| chr20:33534110
|
G | A | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+43809G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33534110 | ||||||
| chr20:33534324
|
T | TTTTG | 62 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(59): Show | 62 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.34+44036_34+44039d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33534324 | |||||
| chr20:33534334
|
T | C | 68 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(65): Show | 68 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.34+44033T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33534334 | ||||||
| chr20:33534519
|
G | T | 1 | a0001c0002t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.34+44218G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33534519 | ||||||
| chr20:33534603
|
G | T | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+44302G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33534603 | ||||||
| chr20:33534751
|
C | CT | 181 | a0001c0001t0001g0245a0001c0001t0003g0071a0001c0001t0003g0072others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.34+44471dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33534751 | |||||
| chr20:33534751
|
C | CTT | 76 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(73): Show | 76 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.34+44470_34+44471d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33534751 | |||||
| chr20:33534864
|
T | A | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.34+44563T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33534864 | ||||||
| chr20:33535063
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+44762A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535063 | ||||||
| chr20:33535064
|
A | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+44763A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535064 | ||||||
| chr20:33535170
|
T | G | 2 | a0001c0002t0016g0193a0001c0002t0035g0202 | 2 | HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.34+44869T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535170 | ||||||
| chr20:33535176
|
G | T | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.34+44875G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535176 | ||||||
| chr20:33535320
|
C | A | 1 | a0001c0002t0002g0196 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.34+45019C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535320 | ||||||
| chr20:33535446
|
CCTT | C | 14 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.34+45146_34+45148d others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535446 | ||||||
| chr20:33535532
|
G | T | 2 | a0001c0001t0003g0135a0001c0001t0014g0184 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.34+45231G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535532 | ||||||
| chr20:33535588
|
A | G | 2 | a0001c0001t0006g0091a0001c0001t0006g0143 | 2 | HG01361.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.34+45287A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535588 | ||||||
| chr20:33535593
|
TTGAG | T | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+45294_34+45297d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33535593 | |||||
| chr20:33535602
|
A | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+45301A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535602 | ||||||
| chr20:33535606
|
T | A | 14 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.34+45305T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535606 | ||||||
| chr20:33535608
|
A | T | 40 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(37): Show | 40 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.34+45307A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535608 | ||||||
| chr20:33535616
|
A | T | 3 | a0001c0001t0018g0120a0001c0001t0018g0121a0001c0001t0030g0001 | 3 | HG01891.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.34+45315A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535616 | ||||||
| chr20:33535619
|
TTTTC | T | 14 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(11): Show | 14 | HG00438.hp1 HG01070.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.34+45322_34+45325d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33535619 | |||||
| chr20:33535620
|
T | A | 1 | a0001c0001t0004g0039 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.34+45319T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535620 | ||||||
| chr20:33535621
|
TTC | T | 19 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(16): Show | 19 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.34+45322_34+45323d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33535621 | |||||
| chr20:33535622
|
T | C | 2 | a0001c0001t0018g0120a0001c0001t0018g0121 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.34+45321T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535622 | ||||||
| chr20:33535623
|
C | A | 2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.34+45322C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535623 | ||||||
| chr20:33535623
|
C | T | 3 | a0001c0001t0004g0039a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01496.hp1 HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.34+45322C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535623 | ||||||
| chr20:33535624
|
T | A | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+45323T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535624 | ||||||
| chr20:33535627
|
T | A | 1 | a0001c0001t0004g0037 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.34+45326T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535627 | ||||||
| chr20:33535628
|
T | A | 3 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0028 | 3 | HG02615.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.34+45327T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535628 | ||||||
| chr20:33535651
|
ATTTAT | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.34+45368_34+45372d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33535651 | |||||
| chr20:33535690
|
T | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+45389T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535690 | ||||||
| chr20:33535818
|
C | T | 1 | a0001c0002t0002g0175 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.34+45517C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33535818 | ||||||
| chr20:33536003
|
C | T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+45702C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536003 | ||||||
| chr20:33536129
|
T | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+45828T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536129 | ||||||
| chr20:33536133
|
A | G | 1 | a0001c0002t0002g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.34+45832A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536133 | ||||||
| chr20:33536159
|
C | T | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+45858C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536159 | ||||||
| chr20:33536160
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+45859G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536160 | ||||||
| chr20:33536170
|
C | T | 1 | a0001c0002t0002g0178 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.34+45869C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536170 | ||||||
| chr20:33536230
|
ATCCCAGT others(121): Show |
A | 4 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0187others(1): Show | 4 | HG00735.hp1 HG01070.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+45965_34+46092d others(2): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33536230 | |||||
| chr20:33536248
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+45947G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536248 | ||||||
| chr20:33536266
|
T | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+45965T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536266 | ||||||
| chr20:33536272
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+45971A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536272 | ||||||
| chr20:33536272
|
A | T | 1 | a0001c0002t0002g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.34+45971A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536272 | ||||||
| chr20:33536303
|
CCCCCCCC others(120): Show |
C | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+46021_34+46147d others(2): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33536303 | |||||
| chr20:33536305
|
C | T | 1 | a0001c0002t0002g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.34+46004C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536305 | ||||||
| chr20:33536321
|
C | T | 1 | a0001c0001t0007g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.34+46020C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536321 | ||||||
| chr20:33536322
|
A | G | 57 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(54): Show | 57 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.34+46021A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536322 | ||||||
| chr20:33536385
|
C | T | 2 | a0001c0002t0002g0288a0001c0002t0009g0290 | 2 | NA19056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.34+46084C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536385 | ||||||
| chr20:33536432
|
C | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+46131C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536432 | ||||||
| chr20:33536432
|
CCCCCCAC others(39): Show |
C | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+46156_34+46201d others(48): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33536432 | |||||
| chr20:33536448
|
C | T | 1 | a0001c0001t0003g0111 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.34+46147C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536448 | ||||||
| chr20:33536466
|
T | G | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+46165T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536466 | ||||||
| chr20:33536499
|
G | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+46198G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536499 | ||||||
| chr20:33536521
|
A | G | 60 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(57): Show | 60 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.34+46220A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536521 | ||||||
| chr20:33536533
|
CCAGACGG others(33): Show |
C | 4 | a0001c0001t0006g0094a0001c0001t0006g0095a0001c0001t0006g0118others(1): Show | 4 | HG00408.hp2 HG00544.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+46242_34+46281d others(42): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33536533 | |||||
| chr20:33536556
|
T | TAGGGGCT others(33): Show |
37 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(34): Show | 37 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.34+46285_34+46324d others(42): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33536556 | |||||
| chr20:33536568
|
A | T | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+46267A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536568 | ||||||
| chr20:33536590
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.34+46289C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536590 | ||||||
| chr20:33536793
|
TACTTCCT others(33): Show |
T | 1 | a0001c0001t0003g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.34+46515_34+46554d others(42): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33536793 | |||||
| chr20:33536850
|
G | T | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+46549G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536850 | ||||||
| chr20:33536851
|
G | C | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+46550G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536851 | ||||||
| chr20:33536866
|
C | T | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.34+46565C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536866 | ||||||
| chr20:33536867
|
G | A | 1 | a0001c0001t0003g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.34+46566G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536867 | ||||||
| chr20:33536946
|
C | T | 1 | a0001c0002t0002g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.34+46645C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536946 | ||||||
| chr20:33536961
|
A | G | 14 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.34+46660A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536961 | ||||||
| chr20:33536986
|
C | T | 2 | a0001c0001t0003g0071a0001c0001t0003g0072 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.34+46685C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33536986 | ||||||
| chr20:33537111
|
C | T | 3 | a0001c0001t0007g0012a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+46810C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537111 | ||||||
| chr20:33537164
|
C | T | 1 | a0001c0001t0007g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.34+46863C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537164 | ||||||
| chr20:33537165
|
G | A | 19 | a0001c0001t0001g0220a0001c0001t0001g0228a0001c0001t0001g0234others(16): Show | 19 | HG00597.hp1 HG00621.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.34+46864G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537165 | ||||||
| chr20:33537199
|
T | C | 42 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(39): Show | 42 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.34+46898T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537199 | ||||||
| chr20:33537293
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.34+46992C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537293 | ||||||
| chr20:33537305
|
C | T | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+47004C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537305 | ||||||
| chr20:33537353
|
A | G | 58 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(55): Show | 58 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.34+47052A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537353 | ||||||
| chr20:33537431
|
G | A | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+47130G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537431 | ||||||
| chr20:33537451
|
C | T | 1 | a0001c0002t0002g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.34+47150C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537451 | ||||||
| chr20:33537453
|
G | T | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+47152G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537453 | ||||||
| chr20:33537462
|
CAGAGGGA others(18): Show |
C | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+47177_34+47201d others(27): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33537462 | |||||
| chr20:33537737
|
G | A | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+47436G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537737 | ||||||
| chr20:33537766
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.34+47465G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537766 | ||||||
| chr20:33537811
|
G | A | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+47510G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537811 | ||||||
| chr20:33537917
|
C | T | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+47616C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33537917 | ||||||
| chr20:33538000
|
T | TA | 14 | a0001c0001t0003g0097a0001c0001t0003g0147a0001c0001t0004g0021others(11): Show | 14 | HG00597.hp2 HG00738.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.34+47713dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33538000 | |||||
| chr20:33538000
|
TA | T | 9 | a0001c0001t0003g0077a0001c0001t0003g0131a0001c0001t0010g0075others(6): Show | 9 | HG00558.hp1 HG01346.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.34+47713delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33538000 | |||||
| chr20:33538064
|
GCTGACGT others(5): Show |
G | 1 | a0001c0001t0007g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.34+47765_34+47776d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33538064 | |||||
| chr20:33538069
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0003g0112 | 2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.34+47768C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33538069 | ||||||
| chr20:33538120
|
T | G | 1 | a0001c0001t0025g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.34+47819T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33538120 | ||||||
| chr20:33538368
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.34+48067T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33538368 | ||||||
| chr20:33538772
|
A | G | 1 | a0001c0001t0010g0150 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.34+48471A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33538772 | ||||||
| chr20:33538974
|
G | A | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+48673G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33538974 | ||||||
| chr20:33539000
|
T | C | 1 | a0001c0001t0003g0104 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.34+48699T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33539000 | ||||||
| chr20:33539064
|
C | T | 1 | a0001c0001t0015g0016 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.34+48763C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33539064 | ||||||
| chr20:33539083
|
T | A | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+48782T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33539083 | ||||||
| chr20:33539101
|
A | G | 1 | a0001c0001t0001g0275 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.34+48800A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33539101 | ||||||
| chr20:33539105
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.34+48804G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33539105 | ||||||
| chr20:33539685
|
G | A | 42 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(39): Show | 42 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.34+49384G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33539685 | ||||||
| chr20:33539687
|
G | GT | 18 | a0001c0001t0001g0250a0001c0001t0001g0270a0001c0001t0003g0089others(15): Show | 18 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.34+49400dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33539687 | |||||
| chr20:33539702
|
G | T | 1 | a0001c0001t0001g0272 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.34+49401G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33539702 | ||||||
| chr20:33539834
|
G | A | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+49533G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33539834 | ||||||
| chr20:33539864
|
T | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0268 | 2 | NA18945.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.34+49563T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33539864 | ||||||
| chr20:33539865
|
A | T | 40 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(37): Show | 40 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.34+49564A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33539865 | ||||||
| chr20:33539968
|
G | T | 2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.34+49667G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33539968 | ||||||
| chr20:33540136
|
C | G | 2 | a0001c0001t0004g0029a0001c0001t0004g0030 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.34+49835C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33540136 | ||||||
| chr20:33540243
|
A | G | 1 | a0001c0004t0006g0093 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.34+49942A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33540243 | ||||||
| chr20:33540387
|
G | A | 1 | a0001c0001t0005g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.34+50086G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33540387 | ||||||
| chr20:33540437
|
G | A | 1 | a0001c0002t0045g0216 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.34+50136G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33540437 | ||||||
| chr20:33540801
|
A | G | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0247others(1): Show | 4 | HG02015.hp1 NA18988.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+50500A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33540801 | ||||||
| chr20:33541074
|
G | A | 2 | a0001c0002t0002g0189a0001c0002t0002g0208 | 2 | HG00741.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.34+50773G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541074 | ||||||
| chr20:33541083
|
T | G | 147 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(144): Show | 147 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.34+50782T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541083 | ||||||
| chr20:33541247
|
G | A | 3 | a0001c0001t0005g0079a0001c0001t0005g0133a0001c0001t0005g0138 | 3 | HG02145.hp1 HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.34+50946G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541247 | ||||||
| chr20:33541262
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.34+50961G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541262 | ||||||
| chr20:33541364
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.34+51063G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541364 | ||||||
| chr20:33541444
|
G | A | 30 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(27): Show | 30 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.34+51143G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541444 | ||||||
| chr20:33541454
|
A | G | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+51153A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541454 | ||||||
| chr20:33541574
|
C | G | 2 | a0001c0001t0004g0029a0001c0001t0004g0030 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.34+51273C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541574 | ||||||
| chr20:33541598
|
A | G | 1 | a0001c0002t0009g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.34+51297A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541598 | ||||||
| chr20:33541767
|
T | G | 1 | a0001c0002t0002g0289 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.34+51466T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541767 | ||||||
| chr20:33541787
|
T | A | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+51486T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541787 | ||||||
| chr20:33541869
|
GGTTTTT | G | 4 | a0001c0004t0006g0093a0001c0004t0006g0140a0001c0004t0006g0142others(1): Show | 4 | HG01123.hp2 HG02109.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+51585_34+51590d others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33541869 | |||||
| chr20:33541991
|
G | A | 1 | a0001c0001t0004g0051 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.34+51690G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33541991 | ||||||
| chr20:33542040
|
A | T | 67 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(64): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.34+51739A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33542040 | ||||||
| chr20:33542114
|
T | C | 60 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(57): Show | 60 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.34+51813T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33542114 | ||||||
| chr20:33542274
|
A | C | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+51973A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33542274 | ||||||
| chr20:33542735
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.34+52434G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33542735 | ||||||
| chr20:33542767
|
G | C | 1 | a0001c0001t0004g0023 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.34+52466G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33542767 | ||||||
| chr20:33542845
|
G | C | 4 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(1): Show | 4 | HG01515.hp1 HG01517.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+52544G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33542845 | ||||||
| chr20:33543052
|
C | T | 1 | a0001c0002t0002g0287 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.34+52751C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33543052 | ||||||
| chr20:33543053
|
G | A | 2 | a0001c0001t0003g0152a0001c0010t0028g0132 | 2 | HG01106.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+52752G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33543053 | ||||||
| chr20:33543261
|
C | T | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.34+52960C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33543261 | ||||||
| chr20:33543283
|
TA | T | 86 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.34+52983delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33543283 | ||||||
| chr20:33543415
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.34+53114A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33543415 | ||||||
| chr20:33543508
|
A | G | 1 | a0001c0001t0003g0087 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.34+53207A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33543508 | ||||||
| chr20:33543515
|
G | T | 4 | a0001c0001t0003g0077a0001c0001t0003g0135a0001c0001t0014g0184others(1): Show | 4 | HG01346.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+53214G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33543515 | ||||||
| chr20:33543571
|
G | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.34+53270G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33543571 | ||||||
| chr20:33543838
|
A | T | 10 | a0001c0001t0003g0131a0001c0001t0004g0026a0001c0001t0006g0083others(7): Show | 10 | HG00558.hp1 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.34+53537A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33543838 | ||||||
| chr20:33543842
|
T | A | 18 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0255others(15): Show | 18 | HG00735.hp2 HG01261.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.34+53541T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33543842 | ||||||
| chr20:33543952
|
C | T | 16 | a0001c0001t0006g0083a0001c0001t0006g0091a0001c0001t0006g0094others(13): Show | 16 | HG00408.hp2 HG00544.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.34+53651C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33543952 | ||||||
| chr20:33544297
|
A | C | 1 | a0001c0001t0004g0040 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.34+53996A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544297 | ||||||
| chr20:33544318
|
C | G | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+54017C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544318 | ||||||
| chr20:33544426
|
C | T | 54 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(51): Show | 54 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.34+54125C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544426 | ||||||
| chr20:33544454
|
G | A | 16 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(13): Show | 16 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+54153G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544454 | ||||||
| chr20:33544743
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+54442C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544743 | ||||||
| chr20:33544791
|
C | T | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.34+54490C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544791 | ||||||
| chr20:33544891
|
A | T | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+54590A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544891 | ||||||
| chr20:33544931
|
TGAATAGA others(8): Show |
T | 1 | a0001c0001t0014g0032 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.34+54644_34+54658d others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544931 | |||||
| chr20:33544940
|
T | TAGAAC | 3 | a0001c0001t0004g0061a0001c0001t0015g0015a0001c0001t0018g0120 | 3 | HG01891.hp2 HG02738.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.34+54644_34+54648d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544940 | |||||
| chr20:33544940
|
T | TAGAACAG others(13): Show |
1 | a0001c0001t0015g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.34+54648_34+54649i others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544940 | |||||
| chr20:33544945
|
C | CAGAACAG others(3): Show |
2 | a0001c0001t0004g0056a0001c0001t0031g0068 | 2 | NA19012.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+54648_34+54649i others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
C | CAGAACAG others(8): Show |
1 | a0001c0001t0004g0048 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.34+54648_34+54649i others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
C | CAGAAT | 13 | a0001c0001t0003g0089a0001c0001t0003g0111a0001c0001t0003g0126others(10): Show | 13 | HG00323.hp2 HG00438.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.34+54709_34+54713d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
C | CAGAATAG others(3): Show |
12 | a0001c0001t0003g0096a0001c0001t0003g0115a0001c0001t0003g0158others(9): Show | 12 | HG01074.hp2 HG01516.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.34+54704_34+54713d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
C | CAGAATAG others(8): Show |
3 | a0001c0001t0003g0153a0001c0001t0005g0138a0001c0001t0008g0007 | 3 | HG02970.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.34+54699_34+54713d others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
C | CAGAATAG others(13): Show |
3 | a0001c0001t0005g0130a0001c0001t0008g0003a0001c0001t0019g0117 | 3 | HG02809.hp2 HG03139.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.34+54694_34+54713d others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
C | CAGAATAG others(18): Show |
2 | a0001c0001t0008g0002a0001c0001t0008g0006 | 2 | HG01261.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.34+54689_34+54713d others(27): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
C | CAGAATAG others(53): Show |
1 | a0001c0001t0038g0116 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.34+54654_34+54713d others(62): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
CAGAAT | C | 73 | a0001c0001t0001g0252a0001c0001t0001g0255a0001c0001t0003g0077others(70): Show | 73 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.34+54709_34+54713d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
CAGAATAG others(3): Show |
C | 39 | a0001c0001t0001g0237a0001c0001t0001g0253a0001c0001t0001g0276others(36): Show | 39 | HG00738.hp1 HG01070.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.34+54704_34+54713d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
CAGAATAG others(5): Show |
C | 1 | a0001c0004t0006g0140 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.34+54646_34+54657d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
CAGAATAG others(8): Show |
C | 46 | a0001c0001t0001g0195a0001c0001t0001g0236a0001c0001t0001g0238others(43): Show | 46 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.34+54699_34+54713d others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
CAGAATAG others(13): Show |
C | 31 | a0001c0001t0001g0159a0001c0001t0001g0220a0001c0001t0001g0224others(28): Show | 31 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.34+54694_34+54713d others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
CAGAATAG others(18): Show |
C | 6 | a0001c0001t0001g0259a0001c0001t0012g0163a0001c0001t0012g0165others(3): Show | 6 | HG02273.hp1 HG02486.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.34+54689_34+54713d others(27): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544945
|
CAGAATAG others(23): Show |
C | 11 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0225others(8): Show | 11 | HG02698.hp1 HG03017.hp1 HG04115.hp1 others(8): Show |
intron_variant | MODIFIER | c.34+54684_34+54713d others(32): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544945 | |||||
| chr20:33544950
|
T | C | 21 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(18): Show | 21 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.34+54649T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544950 | ||||||
| chr20:33544955
|
T | C | 10 | a0001c0001t0004g0025a0001c0001t0004g0039a0001c0001t0004g0042others(7): Show | 10 | HG00438.hp1 HG01496.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.34+54654T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544955 | ||||||
| chr20:33544960
|
T | C | 8 | a0001c0001t0004g0028a0001c0001t0004g0038a0001c0001t0004g0040others(5): Show | 8 | HG01070.hp2 HG02273.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.34+54659T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544960 | ||||||
| chr20:33544965
|
T | C | 7 | a0001c0001t0004g0017a0001c0001t0004g0051a0001c0001t0004g0058others(4): Show | 7 | HG01981.hp1 HG02155.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.34+54664T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544965 | ||||||
| chr20:33544985
|
T | TAGAACAG others(8): Show |
2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.34+54688_34+54689i others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544985 | |||||
| chr20:33544985
|
T | TAGAACAG others(18): Show |
2 | a0001c0001t0004g0024a0001c0001t0036g0018 | 2 | HG01361.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.34+54688_34+54689i others(27): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544985 | |||||
| chr20:33544985
|
T | TAGAACAG others(38): Show |
1 | a0001c0001t0004g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.34+54688_34+54689i others(47): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544985 | |||||
| chr20:33544990
|
T | C | 5 | a0001c0001t0004g0019a0001c0001t0004g0024a0001c0001t0007g0067others(2): Show | 5 | HG01361.hp1 HG02572.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+54689T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544990 | ||||||
| chr20:33544990
|
T | TAGAACAG others(3): Show |
1 | a0001c0001t0004g0023 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.34+54693_34+54694i others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544990 | |||||
| chr20:33544990
|
T | TAGAACAG others(8): Show |
1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.34+54693_34+54694i others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544990 | |||||
| chr20:33544990
|
T | TAGAACAG others(13): Show |
3 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022 | 3 | HG00738.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.34+54693_34+54694i others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544990 | |||||
| chr20:33544990
|
T | TAGAACAG others(18): Show |
4 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0011g0063others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+54693_34+54694i others(27): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544990 | |||||
| chr20:33544990
|
T | TAGAACAG others(23): Show |
1 | a0001c0001t0011g0066 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.34+54693_34+54694i others(32): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33544990 | |||||
| chr20:33544995
|
T | C | 15 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(12): Show | 15 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.34+54694T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33544995 | ||||||
| chr20:33545000
|
T | C | 15 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(12): Show | 15 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.34+54699T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545000 | ||||||
| chr20:33545005
|
T | C | 15 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(12): Show | 15 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.34+54704T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545005 | ||||||
| chr20:33545005
|
TAGAATAG others(3): Show |
T | 1 | a0001c0001t0033g0052 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.34+54709_34+54718d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545005 | |||||
| chr20:33545010
|
T | C | 21 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(18): Show | 21 | HG00408.hp2 HG00544.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.34+54709T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545010 | ||||||
| chr20:33545010
|
T | TAGAAC | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01070.hp1 HG01261.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.34+54719_34+54723d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545010 | |||||
| chr20:33545010
|
T | TAGAACAG others(8): Show |
2 | a0001c0001t0015g0014a0001c0001t0015g0015 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.34+54723_34+54724i others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545010 | |||||
| chr20:33545010
|
T | TAGAACAG others(13): Show |
2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.34+54723_34+54724i others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545010 | |||||
| chr20:33545010
|
T | TAGAACAG others(18): Show |
3 | a0001c0001t0004g0041a0001c0001t0004g0048a0001c0001t0004g0056 | 3 | NA18944.hp2 NA18960.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.34+54723_34+54724i others(27): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545010 | |||||
| chr20:33545010
|
T | TAGAACAG others(23): Show |
7 | a0001c0001t0004g0026a0001c0001t0004g0042a0001c0001t0004g0049others(4): Show | 7 | HG00438.hp1 HG01981.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.34+54723_34+54724i others(32): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545010 | |||||
| chr20:33545010
|
T | TAGAACAG others(28): Show |
10 | a0001c0001t0004g0017a0001c0001t0004g0025a0001c0001t0004g0028others(7): Show | 10 | HG01070.hp2 HG01496.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.34+54723_34+54724i others(37): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545010 | |||||
| chr20:33545010
|
T | TAGAACAG others(33): Show |
2 | a0001c0001t0004g0291a0001c0001t0011g0062 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.34+54723_34+54724i others(42): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545010 | |||||
| chr20:33545010
|
T | TAGAACAG others(48): Show |
1 | a0001c0001t0015g0016 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.34+54723_34+54724i others(57): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545010 | |||||
| chr20:33545010
|
T | TAGAATAG others(3): Show |
1 | a0001c0001t0003g0122 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.34+54713_34+54714i others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545010 | |||||
| chr20:33545010
|
T | TAGAATAG others(13): Show |
1 | a0001c0001t0003g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.34+54713_34+54714i others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545010 | |||||
| chr20:33545015
|
C | CAGAAA | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+54718_34+54719i others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545015 | |||||
| chr20:33545020
|
C | CAGAAT | 78 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(75): Show | 78 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.34+54720_34+54724d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545020 | |||||
| chr20:33545020
|
C | T | 83 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(80): Show | 83 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.34+54719C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545020 | ||||||
| chr20:33545025
|
T | C | 14 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.34+54724T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545025 | ||||||
| chr20:33545093
|
G | A | 2 | a0001c0002t0002g0031a0001c0002t0034g0043 | 2 | NA18983.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.34+54792G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545093 | ||||||
| chr20:33545131
|
CA | C | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+54834delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545131 | |||||
| chr20:33545269
|
T | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+54968T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545269 | ||||||
| chr20:33545439
|
C | CTCTT | 17 | a0001c0001t0004g0048a0001c0001t0005g0084a0001c0001t0013g0197others(14): Show | 17 | HG02080.hp1 HG02622.hp2 HG03209.hp2 others(14): Show |
intron_variant | MODIFIER | c.34+55169_34+55172d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
C | CTCTTTCT others(1): Show |
10 | a0001c0001t0001g0195a0001c0001t0001g0236a0001c0001t0001g0237others(7): Show | 10 | HG00621.hp1 HG02015.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.34+55165_34+55172d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
C | CTCTTTCT others(5): Show |
5 | a0001c0001t0001g0247a0001c0001t0001g0268a0001c0001t0012g0162others(2): Show | 5 | HG01167.hp2 HG02015.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+55161_34+55172d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
C | CTCTTTCT others(9): Show |
21 | a0001c0001t0001g0222a0001c0001t0001g0224a0001c0001t0001g0234others(18): Show | 21 | HG00597.hp1 HG00621.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.34+55157_34+55172d others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
C | CTCTTTCT others(13): Show |
17 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0238others(14): Show | 17 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.34+55153_34+55172d others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
C | CTCTTTCT others(17): Show |
21 | a0001c0001t0001g0225a0001c0001t0001g0240a0001c0001t0001g0245others(18): Show | 21 | HG01175.hp2 HG01243.hp1 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.34+55149_34+55172d others(26): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
C | CTCTTTCT others(21): Show |
10 | a0001c0001t0001g0159a0001c0001t0001g0258a0001c0001t0001g0259others(7): Show | 10 | HG02083.hp1 HG02273.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.34+55145_34+55172d others(30): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
C | CTCTTTCT others(25): Show |
7 | a0001c0001t0001g0241a0001c0001t0001g0279a0001c0001t0007g0067others(4): Show | 7 | HG01261.hp2 HG02132.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.34+55141_34+55172d others(34): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
C | CTCTTTCT others(29): Show |
2 | a0001c0001t0008g0005a0001c0001t0025g0009 | 2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.34+55172_34+55173i others(38): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
C | CTCTTTCT others(37): Show |
1 | a0001c0001t0007g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.34+55172_34+55173i others(46): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
CTCTT | C | 5 | a0001c0001t0003g0100a0001c0001t0004g0019a0001c0001t0004g0024others(2): Show | 5 | HG01361.hp1 HG01361.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.34+55169_34+55172d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
CTCTTTCT others(1): Show |
C | 4 | a0001c0001t0001g0228a0001c0001t0003g0135a0001c0001t0014g0184others(1): Show | 4 | HG02559.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+55165_34+55172d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545439
|
CTCTTTCT others(5): Show |
C | 1 | a0001c0001t0003g0111 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.34+55161_34+55172d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545439 | |||||
| chr20:33545470
|
T | TTTCTTTC others(13): Show |
3 | a0001c0001t0001g0277a0001c0001t0014g0293a0001c0001t0030g0001 | 3 | HG03195.hp2 HG03579.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.34+55172_34+55173i others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545470 | |||||
| chr20:33545470
|
T | TTTCTTTC others(17): Show |
1 | a0001c0001t0011g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.34+55172_34+55173i others(26): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545470 | |||||
| chr20:33545470
|
T | TTTCTTTC others(21): Show |
6 | a0001c0001t0001g0256a0001c0001t0007g0008a0001c0001t0007g0010others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.34+55172_34+55173i others(30): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545470 | |||||
| chr20:33545470
|
T | TTTCTTTC others(32): Show |
1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.34+55172_34+55173i others(41): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545470 | |||||
| chr20:33545474
|
G | T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.34+55173G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545474 | ||||||
| chr20:33545548
|
A | AG | 297 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.34+55249dupG | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545548 | |||||
| chr20:33545597
|
C | T | 14 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(11): Show | 14 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.34+55296C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545597 | ||||||
| chr20:33545678
|
G | C | 86 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.34+55377G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545678 | ||||||
| chr20:33545683
|
G | A | 86 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.34+55382G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545683 | ||||||
| chr20:33545685
|
T | G | 86 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.34+55384T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545685 | ||||||
| chr20:33545794
|
AT | A | 3 | a0001c0001t0004g0019a0001c0001t0004g0024a0001c0001t0036g0018 | 3 | HG01361.hp1 NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.34+55496delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33545794 | |||||
| chr20:33545975
|
T | A | 1 | a0001c0001t0001g0274 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.34+55674T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33545975 | ||||||
| chr20:33546015
|
A | G | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.34+55714A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33546015 | ||||||
| chr20:33546076
|
A | G | 1 | a0001c0001t0007g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.34+55775A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33546076 | ||||||
| chr20:33546327
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.34+56026G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33546327 | ||||||
| chr20:33546426
|
C | CT | 6 | a0001c0001t0005g0136a0001c0001t0015g0014a0001c0002t0002g0207others(3): Show | 6 | HG01074.hp1 HG02559.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.34+56142dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33546426 | |||||
| chr20:33546426
|
CT | C | 12 | a0001c0001t0001g0255a0001c0001t0004g0017a0001c0001t0004g0020others(9): Show | 12 | HG00639.hp1 HG00738.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.34+56142delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33546426 | |||||
| chr20:33546430
|
T | A | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.34+56129T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33546430 | ||||||
| chr20:33546473
|
G | C | 5 | a0001c0002t0016g0170a0001c0002t0016g0190a0001c0002t0016g0193others(2): Show | 5 | HG01255.hp2 HG02148.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.34+56172G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33546473 | ||||||
| chr20:33546480
|
T | G | 4 | a0001c0001t0013g0197a0001c0001t0013g0199a0001c0001t0013g0212others(1): Show | 4 | HG02622.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+56179T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33546480 | ||||||
| chr20:33546572
|
A | G | 16 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0080others(13): Show | 16 | HG01243.hp2 HG02145.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.34+56271A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33546572 | ||||||
| chr20:33546620
|
T | A | 1 | a0001c0001t0005g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.34+56319T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33546620 | ||||||
| chr20:33546640
|
A | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.34+56339A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33546640 | ||||||
| chr20:33546674
|
T | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.34+56373T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33546674 | ||||||
| chr20:33547148
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+56847C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33547148 | ||||||
| chr20:33547149
|
G | A | 2 | a0001c0001t0018g0120a0001c0001t0018g0121 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.34+56848G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33547149 | ||||||
| chr20:33547159
|
A | G | 1 | a0001c0002t0002g0189 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.34+56858A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33547159 | ||||||
| chr20:33547166
|
C | G | 1 | a0001c0001t0007g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.34+56865C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33547166 | ||||||
| chr20:33547374
|
A | G | 1 | a0001c0001t0007g0008 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.34+57073A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33547374 | ||||||
| chr20:33547627
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+57326G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33547627 | ||||||
| chr20:33547687
|
A | ATG | 61 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0238others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.34+57428_34+57429d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33547687 | |||||
| chr20:33547687
|
A | ATGTG | 57 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0235others(54): Show | 57 | HG00323.hp2 HG00597.hp1 HG01175.hp1 others(54): Show |
intron_variant | MODIFIER | c.34+57426_34+57429d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33547687 | |||||
| chr20:33547687
|
A | ATGTGTG | 47 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0225others(44): Show | 47 | HG00621.hp2 HG00639.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.34+57424_34+57429d others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33547687 | |||||
| chr20:33547687
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0001g0241a0001c0001t0007g0010a0001c0002t0045g0216 | 3 | HG02132.hp2 HG03453.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.34+57422_34+57429d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33547687 | |||||
| chr20:33547687
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0005g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.34+57420_34+57429d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33547687 | |||||
| chr20:33547687
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.34+57418_34+57429d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33547687 | |||||
| chr20:33547687
|
ATG | A | 37 | a0001c0001t0001g0259a0001c0001t0004g0017a0001c0001t0004g0023others(34): Show | 37 | HG00738.hp1 HG01109.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.34+57428_34+57429d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33547687 | |||||
| chr20:33547687
|
ATGTG | A | 17 | a0001c0001t0003g0149a0001c0001t0004g0048a0001c0001t0004g0049others(14): Show | 17 | HG01258.hp2 HG02015.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.34+57426_34+57429d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33547687 | |||||
| chr20:33547687
|
ATGTGTG | A | 12 | a0001c0001t0001g0222a0001c0001t0004g0029a0001c0001t0004g0030others(9): Show | 12 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.34+57424_34+57429d others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33547687 | |||||
| chr20:33547687
|
ATGTGTGT others(5): Show |
A | 2 | a0001c0002t0002g0178a0001c0002t0002g0180 | 2 | HG01123.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.34+57418_34+57429d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33547687 | |||||
| chr20:33547732
|
A | G | 1 | a0001c0002t0002g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.34+57431A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33547732 | ||||||
| chr20:33547802
|
A | G | 1 | a0001c0002t0002g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.34+57501A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33547802 | ||||||
| chr20:33547815
|
G | A | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+57514G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33547815 | ||||||
| chr20:33547920
|
GTTACAC | G | 3 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073 | 3 | HG01515.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.34+57622_34+57627d others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33547920 | |||||
| chr20:33548009
|
G | A | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+57708G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33548009 | ||||||
| chr20:33548062
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.34+57761G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33548062 | ||||||
| chr20:33548409
|
A | C | 1 | a0001c0001t0003g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.34+58108A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33548409 | ||||||
| chr20:33548422
|
T | G | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.34+58121T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33548422 | ||||||
| chr20:33548463
|
C | T | 2 | a0001c0001t0018g0120a0001c0001t0018g0121 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.34+58162C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33548463 | ||||||
| chr20:33548497
|
G | A | 1 | a0001c0002t0002g0181 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.34+58196G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33548497 | ||||||
| chr20:33548573
|
G | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+58272G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33548573 | ||||||
| chr20:33548807
|
A | G | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.35-58149A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33548807 | ||||||
| chr20:33548841
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-58115C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33548841 | ||||||
| chr20:33548891
|
G | A | 1 | a0001c0001t0007g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.35-58065G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33548891 | ||||||
| chr20:33548974
|
GTCCA | G | 16 | a0001c0001t0001g0159a0001c0001t0001g0241a0001c0001t0001g0246others(13): Show | 16 | HG00099.hp2 HG00597.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.35-57954_35-57951d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33548974 | |||||
| chr20:33548974
|
GTCCATCC others(1): Show |
G | 42 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(39): Show | 42 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.35-57958_35-57951d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33548974 | |||||
| chr20:33548974
|
GTCCATCC others(5): Show |
G | 4 | a0001c0001t0013g0197a0001c0001t0013g0199a0001c0001t0013g0212others(1): Show | 4 | HG02622.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-57962_35-57951d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33548974 | |||||
| chr20:33549000
|
C | T | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-57956C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33549000 | ||||||
| chr20:33549085
|
T | C | 1 | a0001c0001t0003g0123 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.35-57871T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33549085 | ||||||
| chr20:33549086
|
C | T | 1 | a0001c0001t0003g0123 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.35-57870C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33549086 | ||||||
| chr20:33549277
|
TA | T | 85 | a0001c0001t0001g0272a0001c0001t0003g0071a0001c0001t0003g0072others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.35-57667delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33549277 | |||||
| chr20:33549341
|
C | G | 3 | a0001c0001t0004g0019a0001c0001t0004g0024a0001c0001t0036g0018 | 3 | HG01361.hp1 NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.35-57615C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33549341 | ||||||
| chr20:33549428
|
A | G | 6 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-57528A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33549428 | ||||||
| chr20:33549505
|
G | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-57451G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33549505 | ||||||
| chr20:33549511
|
T | G | 1 | a0001c0001t0017g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.35-57445T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33549511 | ||||||
| chr20:33549695
|
A | G | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-57261A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33549695 | ||||||
| chr20:33549785
|
T | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-57171T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33549785 | ||||||
| chr20:33549861
|
C | CT | 6 | a0001c0001t0037g0296a0001c0001t0040g0295a0001c0002t0002g0169others(3): Show | 6 | HG00438.hp2 HG02109.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.35-57075dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33549861 | |||||
| chr20:33549861
|
CT | C | 59 | a0001c0001t0001g0279a0001c0001t0004g0017a0001c0001t0004g0019others(56): Show | 59 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.35-57075delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33549861 | |||||
| chr20:33550041
|
C | T | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.35-56915C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33550041 | ||||||
| chr20:33550247
|
T | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0280 | 2 | NA18960.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.35-56709T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33550247 | ||||||
| chr20:33550556
|
G | A | 1 | a0001c0002t0002g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.35-56400G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33550556 | ||||||
| chr20:33550572
|
G | A | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.35-56384G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33550572 | ||||||
| chr20:33550587
|
A | T | 1 | a0001c0001t0001g0223 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.35-56369A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33550587 | ||||||
| chr20:33550608
|
G | GTTAT | 23 | a0001c0001t0001g0245a0001c0001t0006g0083a0001c0001t0006g0091others(20): Show | 23 | HG00408.hp2 HG00544.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.35-56323_35-56320d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33550608 | |||||
| chr20:33550608
|
G | GTTATTTA others(1): Show |
31 | a0001c0001t0003g0089a0001c0001t0003g0096a0001c0001t0003g0107others(28): Show | 31 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.35-56327_35-56320d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33550608 | |||||
| chr20:33550608
|
G | GTTATTTA others(5): Show |
49 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(46): Show | 49 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.35-56331_35-56320d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33550608 | |||||
| chr20:33550608
|
G | GTTATTTA others(9): Show |
5 | a0001c0001t0003g0123a0001c0001t0007g0008a0001c0001t0010g0075others(2): Show | 5 | HG02257.hp1 HG03130.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-56335_35-56320d others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33550608 | |||||
| chr20:33550608
|
G | GTTATTTA others(13): Show |
2 | a0001c0001t0007g0010a0001c0001t0007g0013 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.35-56339_35-56320d others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33550608 | |||||
| chr20:33550608
|
GTTAT | G | 6 | a0001c0001t0004g0291a0001c0001t0012g0162a0001c0001t0012g0163others(3): Show | 6 | HG01167.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-56323_35-56320d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33550608 | |||||
| chr20:33550837
|
G | T | 2 | a0001c0001t0004g0291a0001c0001t0004g0292 | 2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.35-56119G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33550837 | ||||||
| chr20:33550994
|
T | A | 1 | a0001c0003t0001g0232 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.35-55962T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33550994 | ||||||
| chr20:33551007
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-55949A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551007 | ||||||
| chr20:33551037
|
T | C | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-55919T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551037 | ||||||
| chr20:33551061
|
T | C | 1 | a0001c0001t0031g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.35-55895T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551061 | ||||||
| chr20:33551092
|
T | C | 1 | a0001c0002t0002g0196 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.35-55864T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551092 | ||||||
| chr20:33551255
|
C | T | 1 | a0001c0002t0002g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.35-55701C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551255 | ||||||
| chr20:33551278
|
G | A | 5 | a0001c0001t0001g0236a0001c0001t0001g0256a0001c0001t0033g0052others(2): Show | 5 | HG01884.hp2 NA18957.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-55678G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551278 | ||||||
| chr20:33551305
|
C | T | 1 | a0001c0002t0002g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.35-55651C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551305 | ||||||
| chr20:33551436
|
G | A | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-55520G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551436 | ||||||
| chr20:33551460
|
C | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-55496C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551460 | ||||||
| chr20:33551539
|
TTTG | T | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.35-55407_35-55405d others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33551539 | |||||
| chr20:33551545
|
G | A | 12 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0251others(9): Show | 12 | HG00735.hp2 HG01243.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.35-55411G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551545 | ||||||
| chr20:33551579
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.35-55377G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551579 | ||||||
| chr20:33551596
|
T | A | 1 | a0001c0004t0006g0140 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.35-55360T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551596 | ||||||
| chr20:33551677
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0042g0194 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.35-55279G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551677 | ||||||
| chr20:33551919
|
C | T | 1 | a0001c0001t0003g0127 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.35-55037C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33551919 | ||||||
| chr20:33552067
|
C | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0246 | 2 | HG02132.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.35-54889C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33552067 | ||||||
| chr20:33552075
|
G | GT | 40 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(37): Show | 40 | HG00438.hp1 HG00738.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.35-54866dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33552075 | |||||
| chr20:33552099
|
A | G | 7 | a0001c0001t0005g0078a0001c0001t0005g0084a0001c0001t0005g0085others(4): Show | 7 | HG02647.hp2 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.35-54857A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33552099 | ||||||
| chr20:33552120
|
A | G | 1 | a0001c0002t0002g0183 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.35-54836A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33552120 | ||||||
| chr20:33552226
|
G | A | 7 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.35-54730G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33552226 | ||||||
| chr20:33552481
|
T | C | 147 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(144): Show | 147 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.35-54475T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33552481 | ||||||
| chr20:33552521
|
C | T | 16 | a0001c0001t0006g0083a0001c0001t0006g0091a0001c0001t0006g0094others(13): Show | 16 | HG00408.hp2 HG00544.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.35-54435C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33552521 | ||||||
| chr20:33552570
|
G | C | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-54386G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33552570 | ||||||
| chr20:33552658
|
G | A | 7 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.35-54298G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33552658 | ||||||
| chr20:33552682
|
G | C | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-54274G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33552682 | ||||||
| chr20:33552768
|
C | G | 14 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.35-54188C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33552768 | ||||||
| chr20:33553182
|
A | T | 1 | a0001c0001t0001g0277 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.35-53774A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33553182 | ||||||
| chr20:33553281
|
A | G | 1 | a0001c0001t0007g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.35-53675A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33553281 | ||||||
| chr20:33553412
|
A | C | 1 | a0001c0002t0017g0124 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.35-53544A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33553412 | ||||||
| chr20:33553560
|
T | C | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.35-53396T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33553560 | ||||||
| chr20:33553781
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.35-53175T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33553781 | ||||||
| chr20:33554065
|
G | A | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.35-52891G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33554065 | ||||||
| chr20:33554211
|
G | A | 54 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(51): Show | 54 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.35-52745G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33554211 | ||||||
| chr20:33554255
|
C | T | 1 | a0001c0002t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.35-52701C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33554255 | ||||||
| chr20:33554260
|
T | C | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.35-52696T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33554260 | ||||||
| chr20:33554270
|
T | C | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.35-52686T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33554270 | ||||||
| chr20:33554333
|
G | A | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-52623G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33554333 | ||||||
| chr20:33554437
|
C | T | 2 | a0001c0001t0008g0004a0001c0001t0008g0005 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.35-52519C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33554437 | ||||||
| chr20:33554530
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.35-52426T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33554530 | ||||||
| chr20:33554558
|
T | TTTTTCTT others(3): Show |
4 | a0001c0001t0013g0197a0001c0001t0013g0199a0001c0001t0013g0212others(1): Show | 4 | HG02622.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-52384_35-52375d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33554558 | |||||
| chr20:33554558
|
TTTTTC | T | 19 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0004g0017others(16): Show | 19 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.35-52379_35-52375d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33554558 | |||||
| chr20:33554594
|
T | C | 1 | a0001c0002t0002g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.35-52362T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33554594 | ||||||
| chr20:33554600
|
C | CT | 27 | a0001c0001t0001g0195a0001c0001t0001g0279a0001c0001t0004g0027others(24): Show | 27 | HG00438.hp1 HG01109.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.35-52333dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33554600 | |||||
| chr20:33554600
|
CT | C | 37 | a0001c0001t0001g0246a0001c0001t0001g0251a0001c0001t0001g0263others(34): Show | 37 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.35-52333delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33554600 | |||||
| chr20:33554600
|
CTT | C | 6 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0015g0014others(3): Show | 6 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-52334_35-52333d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33554600 | |||||
| chr20:33554604
|
T | C | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.35-52352T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33554604 | ||||||
| chr20:33555031
|
C | T | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.35-51925C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33555031 | ||||||
| chr20:33555072
|
G | A | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-51884G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33555072 | ||||||
| chr20:33555231
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35-51725C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33555231 | ||||||
| chr20:33555660
|
C | G | 1 | a0001c0001t0006g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.35-51296C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33555660 | ||||||
| chr20:33555694
|
G | C | 1 | a0001c0003t0001g0281 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.35-51262G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33555694 | ||||||
| chr20:33556136
|
G | A | 68 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(65): Show | 68 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.35-50820G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33556136 | ||||||
| chr20:33556158
|
C | T | 1 | a0001c0001t0017g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.35-50798C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33556158 | ||||||
| chr20:33556209
|
C | G | 1 | a0001c0002t0002g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.35-50747C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33556209 | ||||||
| chr20:33556503
|
G | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-50453G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33556503 | ||||||
| chr20:33556714
|
C | T | 2 | a0001c0001t0003g0123a0001c0001t0003g0131 | 2 | HG00558.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.35-50242C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33556714 | ||||||
| chr20:33556724
|
T | C | 1 | a0001c0001t0008g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.35-50232T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33556724 | ||||||
| chr20:33556824
|
G | A | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-50132G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33556824 | ||||||
| chr20:33557004
|
C | CT | 131 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0223others(128): Show | 131 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.35-49924dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33557004 | |||||
| chr20:33557004
|
C | CTT | 42 | a0001c0001t0001g0222a0001c0001t0001g0241a0001c0001t0001g0245others(39): Show | 42 | HG00323.hp2 HG01106.hp2 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.35-49925_35-49924d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33557004 | |||||
| chr20:33557004
|
C | CTTT | 21 | a0001c0001t0004g0019a0001c0001t0004g0024a0001c0001t0004g0037others(18): Show | 21 | HG00438.hp1 HG01070.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.35-49926_35-49924d others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33557004 | |||||
| chr20:33557004
|
C | CTTTT | 7 | a0001c0001t0003g0110a0001c0001t0003g0134a0001c0001t0004g0025others(4): Show | 7 | HG00099.hp2 HG00639.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.35-49927_35-49924d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33557004 | |||||
| chr20:33557004
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0015g0016 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.35-49936_35-49924d others(15): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33557004 | |||||
| chr20:33557004
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-49938_35-49924d others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33557004 | |||||
| chr20:33557004
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0015g0015 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.35-49950_35-49924d others(29): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33557004 | |||||
| chr20:33557004
|
C | T | 3 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022 | 3 | HG00738.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.35-49952C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33557004 | ||||||
| chr20:33557004
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.35-49933_35-49924d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33557004 | |||||
| chr20:33557059
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.35-49897G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33557059 | ||||||
| chr20:33557536
|
T | TCA | 88 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(85): Show | 88 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.35-49418_35-49417d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33557536 | |||||
| chr20:33557564
|
T | C | 6 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0235others(3): Show | 6 | HG00597.hp1 HG01175.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-49392T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33557564 | ||||||
| chr20:33557960
|
C | G | 1 | a0001c0001t0001g0275 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.35-48996C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33557960 | ||||||
| chr20:33558073
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-48883C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558073 | ||||||
| chr20:33558126
|
C | T | 2 | a0001c0001t0003g0127a0003c0009t0029g0283 | 2 | HG02886.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.35-48830C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558126 | ||||||
| chr20:33558136
|
C | CT | 15 | a0001c0001t0004g0027a0001c0001t0007g0067a0001c0001t0007g0069others(12): Show | 15 | HG01109.hp2 HG01255.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.35-48805dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33558136 | |||||
| chr20:33558138
|
T | C | 3 | a0001c0001t0003g0096a0001c0001t0003g0145a0001c0001t0003g0153 | 3 | HG02615.hp1 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.35-48818T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558138 | ||||||
| chr20:33558386
|
A | G | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.35-48570A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558386 | ||||||
| chr20:33558584
|
C | G | 1 | a0001c0002t0002g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.35-48372C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558584 | ||||||
| chr20:33558602
|
A | C | 2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.35-48354A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558602 | ||||||
| chr20:33558701
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-48255A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558701 | ||||||
| chr20:33558791
|
T | A | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.35-48165T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558791 | ||||||
| chr20:33558823
|
T | TG | 12 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(9): Show | 12 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.35-48126dupG | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33558823 | |||||
| chr20:33558824
|
G | T | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-48132G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558824 | ||||||
| chr20:33558830
|
G | C | 1 | a0001c0002t0002g0201 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.35-48126G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558830 | ||||||
| chr20:33558831
|
C | G | 60 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(57): Show | 60 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.35-48125C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558831 | ||||||
| chr20:33558832
|
G | C | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.35-48124G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558832 | ||||||
| chr20:33558934
|
C | T | 14 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.35-48022C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558934 | ||||||
| chr20:33558956
|
A | AAC | 4 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0255others(1): Show | 4 | HG00735.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-47997_35-47996d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33558956 | |||||
| chr20:33558994
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.35-47962G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33558994 | ||||||
| chr20:33559082
|
CAATT | C | 54 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(51): Show | 54 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.35-47872_35-47869d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33559082 | |||||
| chr20:33559095
|
T | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-47861T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33559095 | ||||||
| chr20:33559172
|
C | CT | 87 | a0001c0001t0001g0220a0001c0001t0001g0242a0001c0001t0001g0243others(84): Show | 87 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.35-47763dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33559172 | |||||
| chr20:33559172
|
C | CTTTTTTT | 7 | a0001c0001t0007g0010a0001c0001t0007g0011a0001c0001t0007g0013others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.35-47769_35-47763d others(9): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33559172 | |||||
| chr20:33559172
|
C | CTTTTTTT others(3): Show |
5 | a0001c0001t0004g0019a0001c0001t0004g0024a0001c0001t0004g0027others(2): Show | 5 | HG01109.hp2 HG01361.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-47772_35-47763d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33559172 | |||||
| chr20:33559172
|
C | CTTTTTTT others(4): Show |
17 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022others(14): Show | 17 | HG00738.hp2 HG01070.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.35-47773_35-47763d others(13): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33559172 | |||||
| chr20:33559172
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0050others(2): Show | 5 | HG02155.hp2 HG02738.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-47774_35-47763d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33559172 | |||||
| chr20:33559172
|
C | CTTTTTTT others(6): Show |
5 | a0001c0001t0004g0017a0001c0001t0004g0023a0001c0001t0004g0042others(2): Show | 5 | HG00438.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-47775_35-47763d others(15): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33559172 | |||||
| chr20:33559172
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0004g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.35-47776_35-47763d others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33559172 | |||||
| chr20:33559172
|
CTTTTT | C | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01261.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-47767_35-47763d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33559172 | |||||
| chr20:33559175
|
T | TC | 3 | a0001c0001t0006g0094a0001c0001t0006g0095a0001c0001t0006g0144 | 3 | HG00408.hp2 HG00544.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.35-47781_35-47780i others(3): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33559175 | ||||||
| chr20:33559193
|
T | TTTTTTTT others(3): Show |
4 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-47763_35-47762i others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33559193 | ||||||
| chr20:33559371
|
A | T | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-47585A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33559371 | ||||||
| chr20:33559374
|
A | G | 3 | a0001c0002t0002g0196a0001c0002t0002g0206a0001c0002t0002g0211 | 3 | HG01891.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.35-47582A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33559374 | ||||||
| chr20:33559426
|
A | G | 60 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(57): Show | 60 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.35-47530A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33559426 | ||||||
| chr20:33559582
|
G | T | 1 | a0001c0002t0002g0210 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.35-47374G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33559582 | ||||||
| chr20:33559632
|
G | A | 2 | a0001c0001t0003g0128a0001c0001t0003g0129 | 2 | NA18941.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.35-47324G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33559632 | ||||||
| chr20:33560005
|
G | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-46951G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560005 | ||||||
| chr20:33560021
|
T | G | 1 | a0004c0007t0002g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.35-46935T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560021 | ||||||
| chr20:33560076
|
C | T | 1 | a0001c0001t0005g0078 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.35-46880C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560076 | ||||||
| chr20:33560078
|
C | T | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01261.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-46878C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560078 | ||||||
| chr20:33560187
|
A | G | 16 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0080others(13): Show | 16 | HG01243.hp2 HG02145.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.35-46769A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560187 | ||||||
| chr20:33560198
|
G | A | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-46758G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560198 | ||||||
| chr20:33560263
|
G | A | 54 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(51): Show | 54 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.35-46693G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560263 | ||||||
| chr20:33560334
|
G | A | 30 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(27): Show | 30 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.35-46622G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560334 | ||||||
| chr20:33560337
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.35-46619T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560337 | ||||||
| chr20:33560418
|
A | G | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.35-46538A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560418 | ||||||
| chr20:33560709
|
A | G | 5 | a0001c0001t0005g0080a0001c0001t0005g0081a0001c0001t0005g0136others(2): Show | 5 | HG01243.hp2 HG03130.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-46247A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560709 | ||||||
| chr20:33560741
|
CTATA | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-46203_35-46200d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33560741 | |||||
| chr20:33560868
|
T | G | 2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.35-46088T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33560868 | ||||||
| chr20:33561016
|
T | C | 1 | a0001c0001t0003g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.35-45940T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33561016 | ||||||
| chr20:33561067
|
A | G | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.35-45889A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33561067 | ||||||
| chr20:33561137
|
A | C | 42 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(39): Show | 42 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.35-45819A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33561137 | ||||||
| chr20:33561237
|
C | T | 4 | a0001c0001t0003g0077a0001c0001t0003g0135a0001c0001t0014g0184others(1): Show | 4 | HG01346.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-45719C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33561237 | ||||||
| chr20:33561251
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.35-45705C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33561251 | ||||||
| chr20:33561321
|
C | A | 4 | a0001c0001t0003g0126a0001c0001t0003g0128a0001c0001t0003g0129others(1): Show | 4 | HG00621.hp1 NA18941.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-45635C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33561321 | ||||||
| chr20:33561632
|
G | C | 3 | a0001c0001t0003g0096a0001c0001t0003g0145a0001c0001t0003g0153 | 3 | HG02615.hp1 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.35-45324G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33561632 | ||||||
| chr20:33562036
|
C | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-44920C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33562036 | ||||||
| chr20:33562652
|
T | C | 12 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(9): Show | 12 | HG02486.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.35-44304T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33562652 | ||||||
| chr20:33562776
|
G | T | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-44180G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33562776 | ||||||
| chr20:33562844
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.35-44112A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33562844 | ||||||
| chr20:33562990
|
G | A | 1 | a0001c0002t0002g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.35-43966G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33562990 | ||||||
| chr20:33563069
|
G | A | 60 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(57): Show | 60 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.35-43887G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33563069 | ||||||
| chr20:33563128
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-43828G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33563128 | ||||||
| chr20:33563188
|
A | G | 1 | a0001c0003t0001g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.35-43768A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33563188 | ||||||
| chr20:33563346
|
T | A | 1 | a0001c0001t0005g0146 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.35-43610T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33563346 | ||||||
| chr20:33563620
|
C | G | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-43336C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33563620 | ||||||
| chr20:33563919
|
A | G | 4 | a0001c0001t0003g0126a0001c0001t0003g0128a0001c0001t0003g0129others(1): Show | 4 | HG00621.hp1 NA18941.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-43037A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33563919 | ||||||
| chr20:33564036
|
C | T | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.35-42920C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564036 | ||||||
| chr20:33564068
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-42888C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564068 | ||||||
| chr20:33564107
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.35-42849A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564107 | ||||||
| chr20:33564257
|
T | C | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.35-42699T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564257 | ||||||
| chr20:33564263
|
TTC | T | 39 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(36): Show | 39 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.35-42691_35-42690d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33564263 | |||||
| chr20:33564356
|
G | A | 2 | a0001c0001t0004g0058a0001c0001t0030g0001 | 2 | HG02155.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.35-42600G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564356 | ||||||
| chr20:33564404
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-42552C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564404 | ||||||
| chr20:33564446
|
C | T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-42510C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564446 | ||||||
| chr20:33564467
|
G | A | 1 | a0001c0005t0002g0179 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.35-42489G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564467 | ||||||
| chr20:33564487
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.35-42469A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564487 | ||||||
| chr20:33564497
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-42459C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564497 | ||||||
| chr20:33564546
|
C | T | 1 | a0001c0002t0002g0175 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.35-42410C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564546 | ||||||
| chr20:33564750
|
TG | T | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.35-42204delG | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33564750 | |||||
| chr20:33564831
|
C | T | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.35-42125C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564831 | ||||||
| chr20:33564926
|
T | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-42030T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564926 | ||||||
| chr20:33564932
|
C | T | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-42024C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564932 | ||||||
| chr20:33564989
|
G | A | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.35-41967G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33564989 | ||||||
| chr20:33565010
|
C | G | 1 | a0001c0001t0007g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.35-41946C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33565010 | ||||||
| chr20:33565067
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.35-41889C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33565067 | ||||||
| chr20:33565102
|
G | A | 1 | a0001c0002t0016g0193 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.35-41854G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33565102 | ||||||
| chr20:33565106
|
A | T | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.35-41850A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33565106 | ||||||
| chr20:33565459
|
A | G | 1 | a0001c0001t0015g0015 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.35-41497A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33565459 | ||||||
| chr20:33565915
|
C | T | 1 | a0001c0001t0015g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.35-41041C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33565915 | ||||||
| chr20:33566549
|
G | T | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-40407G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33566549 | ||||||
| chr20:33566605
|
CA | C | 59 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(56): Show | 59 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.35-40338delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33566605 | |||||
| chr20:33566689
|
C | T | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.35-40267C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33566689 | ||||||
| chr20:33566989
|
G | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-39967G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33566989 | ||||||
| chr20:33567075
|
A | G | 1 | a0001c0001t0040g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.35-39881A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33567075 | ||||||
| chr20:33567424
|
G | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-39532G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33567424 | ||||||
| chr20:33567668
|
C | T | 1 | a0001c0002t0002g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.35-39288C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33567668 | ||||||
| chr20:33567684
|
G | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-39272G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33567684 | ||||||
| chr20:33567746
|
T | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-39210T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33567746 | ||||||
| chr20:33567869
|
C | G | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.35-39087C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33567869 | ||||||
| chr20:33567969
|
T | C | 2 | a0001c0001t0018g0120a0001c0001t0018g0121 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.35-38987T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33567969 | ||||||
| chr20:33568130
|
C | G | 42 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(39): Show | 42 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.35-38826C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33568130 | ||||||
| chr20:33568275
|
T | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-38681T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33568275 | ||||||
| chr20:33568543
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-38413C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33568543 | ||||||
| chr20:33568565
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.35-38391G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33568565 | ||||||
| chr20:33568775
|
A | G | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-38181A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33568775 | ||||||
| chr20:33568834
|
A | G | 1 | a0001c0001t0003g0087 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.35-38122A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33568834 | ||||||
| chr20:33568893
|
T | C | 3 | a0001c0001t0003g0126a0001c0001t0003g0128a0001c0001t0003g0129 | 3 | NA18941.hp2 NA18979.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.35-38063T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33568893 | ||||||
| chr20:33568994
|
G | C | 3 | a0001c0001t0003g0096a0001c0001t0003g0145a0001c0001t0003g0153 | 3 | HG02615.hp1 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.35-37962G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33568994 | ||||||
| chr20:33570128
|
G | A | 147 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(144): Show | 147 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.35-36828G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570128 | ||||||
| chr20:33570139
|
G | A | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.35-36817G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570139 | ||||||
| chr20:33570169
|
T | C | 7 | a0001c0001t0003g0101a0001c0001t0003g0104a0001c0001t0003g0105others(4): Show | 7 | HG00408.hp1 HG02080.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.35-36787T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570169 | ||||||
| chr20:33570177
|
A | C | 1 | a0001c0002t0002g0205 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.35-36779A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570177 | ||||||
| chr20:33570241
|
A | G | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-36715A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570241 | ||||||
| chr20:33570282
|
A | T | 2 | a0001c0001t0003g0123a0001c0001t0003g0131 | 2 | HG00558.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.35-36674A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570282 | ||||||
| chr20:33570283
|
AAAAC | A | 42 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(39): Show | 42 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.35-36661_35-36658d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33570283 | |||||
| chr20:33570323
|
C | A | 1 | a0001c0001t0025g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.35-36633C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570323 | ||||||
| chr20:33570344
|
G | A | 1 | a0001c0001t0040g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.35-36612G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570344 | ||||||
| chr20:33570392
|
A | G | 2 | a0001c0001t0019g0082a0001c0001t0019g0117 | 2 | NA18971.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.35-36564A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570392 | ||||||
| chr20:33570524
|
CAG | C | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-36429_35-36428d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33570524 | |||||
| chr20:33570635
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.35-36321A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570635 | ||||||
| chr20:33570657
|
T | C | 1 | a0001c0001t0006g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.35-36299T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570657 | ||||||
| chr20:33570777
|
C | G | 67 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(64): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.35-36179C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33570777 | ||||||
| chr20:33571261
|
C | T | 85 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.35-35695C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33571261 | ||||||
| chr20:33571536
|
C | T | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-35420C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33571536 | ||||||
| chr20:33571769
|
G | C | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.35-35187G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33571769 | ||||||
| chr20:33571930
|
G | A | 2 | a0001c0001t0018g0120a0001c0001t0018g0121 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.35-35026G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33571930 | ||||||
| chr20:33571943
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.35-35013T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33571943 | ||||||
| chr20:33572140
|
A | G | 1 | a0002c0008t0002g0047 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.35-34816A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33572140 | ||||||
| chr20:33572215
|
A | C | 4 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-34741A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33572215 | ||||||
| chr20:33572411
|
A | T | 1 | a0001c0001t0003g0131 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.35-34545A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33572411 | ||||||
| chr20:33572529
|
A | G | 2 | a0001c0001t0003g0097a0001c0001t0003g0147 | 2 | HG00597.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.35-34427A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33572529 | ||||||
| chr20:33572721
|
A | G | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.35-34235A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33572721 | ||||||
| chr20:33572798
|
G | C | 1 | a0001c0003t0001g0229 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.35-34158G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33572798 | ||||||
| chr20:33572920
|
A | C | 30 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(27): Show | 30 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.35-34036A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33572920 | ||||||
| chr20:33573446
|
G | T | 1 | a0002c0008t0002g0047 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.35-33510G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33573446 | ||||||
| chr20:33573604
|
C | T | 1 | a0001c0002t0002g0183 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.35-33352C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33573604 | ||||||
| chr20:33573634
|
A | C | 66 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(63): Show | 66 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.35-33322A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33573634 | ||||||
| chr20:33573871
|
C | A | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.35-33085C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33573871 | ||||||
| chr20:33573908
|
A | G | 62 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(59): Show | 62 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.35-33048A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33573908 | ||||||
| chr20:33573918
|
C | CT | 38 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(35): Show | 38 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.35-33037dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33573918 | |||||
| chr20:33573956
|
A | AT | 17 | a0001c0001t0003g0147a0001c0001t0007g0008a0001c0001t0007g0010others(14): Show | 17 | HG01261.hp2 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.35-32987dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33573956 | |||||
| chr20:33574014
|
C | T | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.35-32942C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33574014 | ||||||
| chr20:33574036
|
A | G | 1 | a0001c0002t0002g0210 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.35-32920A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33574036 | ||||||
| chr20:33574231
|
G | A | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-32725G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33574231 | ||||||
| chr20:33574261
|
G | C | 1 | a0001c0002t0002g0177 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.35-32695G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33574261 | ||||||
| chr20:33574388
|
G | A | 1 | a0001c0002t0002g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.35-32568G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33574388 | ||||||
| chr20:33574439
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-32517A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33574439 | ||||||
| chr20:33574683
|
C | G | 60 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(57): Show | 60 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.35-32273C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33574683 | ||||||
| chr20:33574736
|
T | C | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-32220T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33574736 | ||||||
| chr20:33574915
|
A | G | 217 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(214): Show | 217 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.35-32041A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33574915 | ||||||
| chr20:33575266
|
C | G | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-31690C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33575266 | ||||||
| chr20:33575313
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02300.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.35-31643G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33575313 | ||||||
| chr20:33575482
|
T | G | 1 | a0001c0002t0002g0185 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.35-31474T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33575482 | ||||||
| chr20:33575486
|
G | A | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-31470G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33575486 | ||||||
| chr20:33575624
|
T | C | 297 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.35-31332T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33575624 | ||||||
| chr20:33575755
|
A | G | 3 | a0001c0002t0002g0167a0001c0002t0002g0187a0001c0002t0002g0204 | 3 | HG00735.hp1 HG02523.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.35-31201A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33575755 | ||||||
| chr20:33575816
|
C | T | 1 | a0001c0001t0006g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.35-31140C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33575816 | ||||||
| chr20:33575977
|
C | T | 16 | a0001c0001t0006g0083a0001c0001t0006g0091a0001c0001t0006g0094others(13): Show | 16 | HG00408.hp2 HG00544.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.35-30979C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33575977 | ||||||
| chr20:33576029
|
C | T | 1 | a0001c0002t0002g0053 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.35-30927C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33576029 | ||||||
| chr20:33576161
|
A | T | 6 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-30795A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33576161 | ||||||
| chr20:33576231
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-30725A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33576231 | ||||||
| chr20:33576274
|
C | G | 1 | a0004c0007t0002g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.35-30682C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33576274 | ||||||
| chr20:33576328
|
G | C | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.35-30628G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33576328 | ||||||
| chr20:33576765
|
A | G | 1 | a0001c0001t0037g0296 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.35-30191A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33576765 | ||||||
| chr20:33576901
|
G | A | 1 | a0001c0001t0011g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.35-30055G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33576901 | ||||||
| chr20:33576959
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-29997A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33576959 | ||||||
| chr20:33577146
|
G | T | 1 | a0001c0002t0002g0207 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.35-29810G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33577146 | ||||||
| chr20:33577207
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.35-29749G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33577207 | ||||||
| chr20:33577269
|
A | G | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.35-29687A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33577269 | ||||||
| chr20:33577304
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-29652A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33577304 | ||||||
| chr20:33577535
|
G | A | 1 | a0001c0002t0002g0196 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.35-29421G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33577535 | ||||||
| chr20:33577561
|
G | A | 1 | a0001c0002t0002g0045 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.35-29395G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33577561 | ||||||
| chr20:33577706
|
G | A | 3 | a0001c0001t0007g0067a0001c0001t0007g0069a0003c0009t0029g0283 | 3 | HG02572.hp1 HG02886.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.35-29250G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33577706 | ||||||
| chr20:33577944
|
A | G | 4 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0235others(1): Show | 4 | HG00597.hp1 HG01175.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-29012A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33577944 | ||||||
| chr20:33578007
|
C | A | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.35-28949C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33578007 | ||||||
| chr20:33578156
|
C | T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-28800C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33578156 | ||||||
| chr20:33578698
|
A | G | 1 | a0001c0001t0003g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.35-28258A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33578698 | ||||||
| chr20:33578846
|
G | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-28110G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33578846 | ||||||
| chr20:33578918
|
A | C | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-28038A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33578918 | ||||||
| chr20:33579104
|
G | GTT | 5 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(2): Show | 5 | HG01070.hp2 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-27852_35-27851i others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33579104 | ||||||
| chr20:33579105
|
G | GTT | 7 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0041others(4): Show | 7 | HG00438.hp1 HG02155.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.35-27843_35-27842d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33579105 | |||||
| chr20:33579105
|
G | T | 9 | a0001c0001t0001g0225a0001c0001t0004g0037a0001c0001t0004g0038others(6): Show | 9 | HG01070.hp2 HG01496.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.35-27851G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33579105 | ||||||
| chr20:33579115
|
G | GT | 16 | a0001c0001t0003g0073a0001c0001t0003g0109a0001c0001t0003g0113others(13): Show | 16 | HG01169.hp2 HG01346.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.35-27826dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33579115 | |||||
| chr20:33579115
|
G | GTT | 12 | a0001c0001t0001g0257a0001c0001t0004g0017a0001c0001t0004g0019others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.35-27827_35-27826d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33579115 | |||||
| chr20:33579115
|
G | T | 17 | a0001c0001t0001g0225a0001c0001t0004g0029a0001c0001t0004g0030others(14): Show | 17 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.35-27841G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33579115 | ||||||
| chr20:33579123
|
T | G | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-27833T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33579123 | ||||||
| chr20:33579235
|
A | G | 5 | a0001c0002t0002g0286a0001c0002t0002g0287a0001c0002t0002g0288others(2): Show | 5 | NA18944.hp1 NA18994.hp2 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-27721A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33579235 | ||||||
| chr20:33579554
|
C | CT | 15 | a0001c0001t0001g0235a0001c0001t0001g0257a0001c0001t0001g0264others(12): Show | 15 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.35-27385dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33579554 | |||||
| chr20:33579605
|
A | G | 1 | a0001c0001t0015g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.35-27351A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33579605 | ||||||
| chr20:33579799
|
GTCTC | G | 5 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016others(2): Show | 5 | HG02559.hp1 HG02630.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-27141_35-27138d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33579799 | |||||
| chr20:33579817
|
C | CT | 9 | a0001c0002t0002g0031a0001c0002t0002g0166a0001c0002t0002g0177others(6): Show | 9 | HG00099.hp1 HG01074.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.35-27125dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33579817 | |||||
| chr20:33579817
|
CT | C | 203 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(200): Show | 203 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.35-27125delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33579817 | |||||
| chr20:33579819
|
T | C | 1 | a0001c0001t0018g0121 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.35-27137T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33579819 | ||||||
| chr20:33579885
|
G | T | 16 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(13): Show | 16 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.35-27071G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33579885 | ||||||
| chr20:33579969
|
C | T | 2 | a0001c0001t0004g0029a0001c0001t0004g0030 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.35-26987C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33579969 | ||||||
| chr20:33580114
|
G | A | 4 | a0001c0001t0006g0094a0001c0001t0006g0095a0001c0001t0006g0118others(1): Show | 4 | HG00408.hp2 HG00544.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-26842G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33580114 | ||||||
| chr20:33580407
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-26549C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33580407 | ||||||
| chr20:33580645
|
A | G | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-26311A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33580645 | ||||||
| chr20:33581095
|
A | G | 59 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(56): Show | 59 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.35-25861A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33581095 | ||||||
| chr20:33581124
|
C | T | 1 | a0001c0002t0002g0033 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.35-25832C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33581124 | ||||||
| chr20:33581311
|
C | A | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.35-25645C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33581311 | ||||||
| chr20:33581417
|
T | C | 16 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(13): Show | 16 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.35-25539T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33581417 | ||||||
| chr20:33581480
|
T | TTG | 16 | a0001c0001t0003g0156a0001c0001t0007g0067a0001c0001t0007g0069others(13): Show | 16 | HG02109.hp2 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.35-25456_35-25455d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33581480 | |||||
| chr20:33581480
|
T | TTGTGTGT others(1): Show |
5 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(2): Show | 5 | HG01167.hp2 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-25462_35-25455d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33581480 | |||||
| chr20:33581735
|
T | C | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-25221T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33581735 | ||||||
| chr20:33581794
|
A | G | 147 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(144): Show | 147 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.35-25162A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33581794 | ||||||
| chr20:33581916
|
A | G | 6 | a0001c0002t0002g0033a0001c0002t0002g0036a0001c0002t0002g0044others(3): Show | 6 | HG02080.hp1 NA18939.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.35-25040A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33581916 | ||||||
| chr20:33582119
|
T | C | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-24837T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33582119 | ||||||
| chr20:33582418
|
G | T | 42 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(39): Show | 42 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.35-24538G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33582418 | ||||||
| chr20:33582602
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0280 | 2 | NA18960.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.35-24354C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33582602 | ||||||
| chr20:33582716
|
C | T | 2 | a0001c0001t0004g0029a0001c0001t0004g0030 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.35-24240C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33582716 | ||||||
| chr20:33582927
|
G | A | 54 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(51): Show | 54 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.35-24029G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33582927 | ||||||
| chr20:33582938
|
T | TA | 8 | a0001c0001t0004g0041a0001c0001t0004g0048a0001c0001t0004g0056others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.35-24005dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33582938 | |||||
| chr20:33583054
|
G | A | 42 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(39): Show | 42 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.35-23902G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583054 | ||||||
| chr20:33583115
|
C | G | 2 | a0001c0001t0011g0063a0001c0001t0011g0064 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.35-23841C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583115 | ||||||
| chr20:33583230
|
T | C | 2 | a0001c0002t0002g0189a0001c0002t0002g0208 | 2 | HG00741.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.35-23726T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583230 | ||||||
| chr20:33583252
|
G | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-23704G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583252 | ||||||
| chr20:33583415
|
A | G | 1 | a0001c0001t0007g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.35-23541A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583415 | ||||||
| chr20:33583439
|
C | A | 5 | a0001c0002t0002g0031a0001c0002t0002g0046a0001c0002t0017g0124others(2): Show | 5 | HG02135.hp2 NA18943.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-23517C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583439 | ||||||
| chr20:33583440
|
G | A | 1 | a0001c0002t0002g0053 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.35-23516G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583440 | ||||||
| chr20:33583494
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-23462A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583494 | ||||||
| chr20:33583904
|
A | G | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.35-23052A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583904 | ||||||
| chr20:33583910
|
TTTTA | T | 18 | a0001c0001t0001g0220a0001c0001t0001g0234a0001c0001t0001g0235others(15): Show | 18 | HG00597.hp1 HG00621.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.35-23026_35-23023d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33583910 | |||||
| chr20:33583930
|
A | G | 8 | a0001c0001t0001g0159a0001c0001t0003g0109a0001c0001t0004g0054others(5): Show | 8 | HG01070.hp1 HG01258.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.35-23026A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583930 | ||||||
| chr20:33583942
|
G | T | 1 | a0001c0001t0003g0145 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.35-23014G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583942 | ||||||
| chr20:33583954
|
A | G | 62 | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(59): Show | 62 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.35-23002A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583954 | ||||||
| chr20:33583958
|
A | G | 5 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016others(2): Show | 5 | HG02559.hp1 HG02630.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-22998A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33583958 | ||||||
| chr20:33584016
|
T | G | 1 | a0001c0002t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.35-22940T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33584016 | ||||||
| chr20:33584204
|
C | T | 1 | a0001c0002t0002g0060 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.35-22752C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33584204 | ||||||
| chr20:33584319
|
A | G | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-22637A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33584319 | ||||||
| chr20:33584362
|
T | C | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.35-22594T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33584362 | ||||||
| chr20:33584380
|
C | T | 68 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(65): Show | 68 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.35-22576C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33584380 | ||||||
| chr20:33584530
|
T | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-22426T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33584530 | ||||||
| chr20:33584532
|
C | T | 1 | a0001c0001t0008g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.35-22424C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33584532 | ||||||
| chr20:33584553
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0276 | 2 | HG01243.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.35-22403G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33584553 | ||||||
| chr20:33584576
|
G | C | 1 | a0001c0001t0001g0249 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.35-22380G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33584576 | ||||||
| chr20:33584843
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-22113A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33584843 | ||||||
| chr20:33584987
|
A | T | 62 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(59): Show | 62 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.35-21969A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33584987 | ||||||
| chr20:33585260
|
A | T | 1 | a0001c0001t0001g0237 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.35-21696A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33585260 | ||||||
| chr20:33585262
|
A | G | 1 | a0001c0001t0006g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.35-21694A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33585262 | ||||||
| chr20:33585274
|
A | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.35-21682A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33585274 | ||||||
| chr20:33585412
|
A | G | 1 | a0001c0001t0032g0070 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.35-21544A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33585412 | ||||||
| chr20:33585686
|
C | T | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-21270C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33585686 | ||||||
| chr20:33585738
|
A | T | 1 | a0001c0002t0002g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.35-21218A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33585738 | ||||||
| chr20:33585861
|
G | T | 2 | a0001c0001t0003g0071a0001c0001t0003g0072 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.35-21095G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33585861 | ||||||
| chr20:33585923
|
T | G | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.35-21033T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33585923 | ||||||
| chr20:33585938
|
G | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-21018G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33585938 | ||||||
| chr20:33586098
|
A | G | 5 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016others(2): Show | 5 | HG02559.hp1 HG02630.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-20858A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33586098 | ||||||
| chr20:33586116
|
A | G | 1 | a0001c0002t0027g0213 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.35-20840A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33586116 | ||||||
| chr20:33586165
|
TC | T | 10 | a0001c0003t0001g0226a0001c0003t0001g0227a0001c0003t0001g0229others(7): Show | 10 | NA18941.hp1 NA18968.hp1 NA18982.hp2 others(7): Show |
intron_variant | MODIFIER | c.35-20790delC | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33586165 | ||||||
| chr20:33586205
|
G | A | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.35-20751G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33586205 | ||||||
| chr20:33586242
|
A | G | 294 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.35-20714A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33586242 | ||||||
| chr20:33586298
|
C | T | 65 | a0001c0001t0001g0159a0001c0001t0001g0220a0001c0001t0001g0222others(62): Show | 65 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.35-20658C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33586298 | ||||||
| chr20:33586479
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.35-20477C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33586479 | ||||||
| chr20:33586576
|
T | C | 6 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-20380T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33586576 | ||||||
| chr20:33586736
|
G | A | 7 | a0001c0002t0002g0166a0001c0002t0002g0177a0001c0002t0002g0203others(4): Show | 7 | HG00099.hp1 HG01074.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.35-20220G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33586736 | ||||||
| chr20:33586998
|
A | G | 11 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(8): Show | 11 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.35-19958A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33586998 | ||||||
| chr20:33587066
|
C | T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-19890C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33587066 | ||||||
| chr20:33587256
|
TTTTTG | T | 69 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(66): Show | 69 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.35-19674_35-19670d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33587256 | |||||
| chr20:33587256
|
TTTTTGTT others(3): Show |
T | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.35-19679_35-19670d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33587256 | |||||
| chr20:33587297
|
C | T | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-19659C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33587297 | ||||||
| chr20:33587428
|
G | A | 2 | a0001c0001t0001g0275a0001c0001t0001g0279 | 2 | HG03710.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.35-19528G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33587428 | ||||||
| chr20:33587440
|
A | G | 215 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(212): Show | 215 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.35-19516A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33587440 | ||||||
| chr20:33587447
|
T | C | 75 | a0001c0001t0001g0257a0001c0001t0003g0071a0001c0001t0003g0072others(72): Show | 75 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.35-19509T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33587447 | ||||||
| chr20:33587467
|
C | T | 218 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(215): Show | 218 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.35-19489C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33587467 | ||||||
| chr20:33587546
|
G | A | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-19410G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33587546 | ||||||
| chr20:33587558
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.35-19398G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33587558 | ||||||
| chr20:33588030
|
A | G | 16 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0080others(13): Show | 16 | HG01243.hp2 HG02145.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.35-18926A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33588030 | ||||||
| chr20:33588071
|
A | G | 1 | a0001c0002t0002g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.35-18885A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33588071 | ||||||
| chr20:33588320
|
A | T | 9 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0251others(6): Show | 9 | HG00735.hp2 HG01243.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.35-18636A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33588320 | ||||||
| chr20:33588359
|
A | AAT | 5 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-18585_35-18584d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33588359 | |||||
| chr20:33588359
|
AAT | A | 3 | a0001c0001t0008g0002a0001c0001t0031g0068a0001c0001t0032g0070 | 3 | HG01261.hp2 HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.35-18585_35-18584d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33588359 | |||||
| chr20:33588381
|
T | C | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.35-18575T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33588381 | ||||||
| chr20:33588528
|
A | T | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-18428A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33588528 | ||||||
| chr20:33588700
|
A | T | 1 | a0001c0001t0011g0062 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.35-18256A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33588700 | ||||||
| chr20:33588741
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.35-18215G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33588741 | ||||||
| chr20:33589127
|
A | G | 2 | a0001c0001t0003g0109a0001c0001t0003g0113 | 2 | HG02257.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.35-17829A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33589127 | ||||||
| chr20:33589273
|
T | C | 85 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.35-17683T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33589273 | ||||||
| chr20:33589626
|
G | A | 2 | a0001c0001t0018g0120a0001c0001t0018g0121 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.35-17330G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33589626 | ||||||
| chr20:33589674
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.35-17282G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33589674 | ||||||
| chr20:33589994
|
T | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-16962T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33589994 | ||||||
| chr20:33590077
|
T | TA | 7 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.35-16868dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33590077 | |||||
| chr20:33590232
|
G | A | 13 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(10): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.35-16724G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33590232 | ||||||
| chr20:33590248
|
C | CA | 14 | a0001c0001t0005g0133a0001c0001t0007g0067a0001c0001t0007g0069others(11): Show | 14 | HG01255.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.35-16692dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33590248 | |||||
| chr20:33590248
|
CA | C | 7 | a0001c0001t0003g0090a0001c0001t0003g0096a0001c0001t0003g0145others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.35-16692delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33590248 | |||||
| chr20:33590425
|
TG | T | 6 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-16530delG | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33590425 | ||||||
| chr20:33590570
|
C | T | 1 | a0001c0002t0002g0177 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.35-16386C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33590570 | ||||||
| chr20:33590699
|
T | C | 1 | a0001c0001t0006g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.35-16257T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33590699 | ||||||
| chr20:33590932
|
T | C | 1 | a0001c0002t0002g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.35-16024T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33590932 | ||||||
| chr20:33591103
|
C | T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-15853C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33591103 | ||||||
| chr20:33591179
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0004g0017 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.35-15767_35-15766i others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33591179 | |||||
| chr20:33591179
|
C | CAAAAAAA others(6): Show |
16 | a0001c0001t0003g0090a0001c0001t0003g0100a0001c0001t0003g0106others(13): Show | 16 | HG00099.hp2 HG00738.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.35-15767_35-15766i others(15): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33591179 | |||||
| chr20:33591179
|
C | CAAAAAAA others(7): Show |
106 | a0001c0001t0001g0234a0001c0001t0001g0255a0001c0001t0001g0256others(103): Show | 106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.35-15767_35-15766i others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33591179 | |||||
| chr20:33591179
|
C | CAAAAAAA others(8): Show |
75 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0222others(72): Show | 75 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.35-15767_35-15766i others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33591179 | |||||
| chr20:33591179
|
C | CAAAAAAA others(9): Show |
7 | a0001c0001t0001g0220a0001c0001t0001g0236a0001c0001t0003g0154others(4): Show | 7 | HG00621.hp1 HG01255.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.35-15767_35-15766i others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33591179 | |||||
| chr20:33591179
|
C | CAAAAAAA others(10): Show |
12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.35-15767_35-15766i others(19): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33591179 | |||||
| chr20:33591182
|
A | G | 4 | a0001c0002t0002g0192a0001c0005t0002g0179a0001c0005t0002g0182others(1): Show | 4 | HG00639.hp1 HG01346.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-15774A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33591182 | ||||||
| chr20:33591273
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-15683C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33591273 | ||||||
| chr20:33591302
|
G | A | 1 | a0001c0002t0002g0188 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.35-15654G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33591302 | ||||||
| chr20:33591406
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0264 | 2 | HG02083.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.35-15550C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33591406 | ||||||
| chr20:33591467
|
C | CA | 13 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(10): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.35-15471dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33591467 | |||||
| chr20:33591467
|
CA | C | 142 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0222others(139): Show | 142 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.35-15471delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33591467 | |||||
| chr20:33591467
|
CAA | C | 6 | a0001c0001t0001g0263a0001c0001t0003g0100a0001c0001t0003g0110others(3): Show | 6 | HG00099.hp2 HG00558.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.35-15472_35-15471d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33591467 | |||||
| chr20:33591467
|
CAAAAAAA others(5): Show |
C | 35 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(32): Show | 35 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.35-15482_35-15471d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33591467 | |||||
| chr20:33591626
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.35-15330G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33591626 | ||||||
| chr20:33591660
|
C | T | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.35-15296C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33591660 | ||||||
| chr20:33591863
|
G | A | 4 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-15093G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33591863 | ||||||
| chr20:33591864
|
G | A | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-15092G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33591864 | ||||||
| chr20:33591864
|
G | C | 2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.35-15092G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33591864 | ||||||
| chr20:33592137
|
C | T | 1 | a0002c0008t0002g0047 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.35-14819C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33592137 | ||||||
| chr20:33592144
|
C | T | 13 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(10): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.35-14812C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33592144 | ||||||
| chr20:33592290
|
G | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-14666G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33592290 | ||||||
| chr20:33592366
|
A | AAAAAATT others(26): Show |
1 | a0001c0001t0004g0040 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.35-14582_35-14550d others(35): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33592366 | |||||
| chr20:33592372
|
T | A | 1 | a0001c0003t0001g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.35-14584T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33592372 | ||||||
| chr20:33592372
|
T | TTA | 3 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073 | 3 | HG01515.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.35-14583_35-14582i others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33592372 | |||||
| chr20:33592374
|
T | A | 3 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073 | 3 | HG01515.hp1 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.35-14582T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33592374 | ||||||
| chr20:33592374
|
T | TTA | 82 | a0001c0001t0003g0077a0001c0001t0003g0089a0001c0001t0003g0090others(79): Show | 82 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.35-14565_35-14564d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33592374 | |||||
| chr20:33592374
|
T | TTATA | 63 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(60): Show | 63 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.35-14567_35-14564d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33592374 | |||||
| chr20:33592374
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0257 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.35-14575_35-14564d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33592374 | |||||
| chr20:33592374
|
TTA | T | 3 | a0001c0001t0030g0001a0001c0001t0032g0070a0001c0010t0028g0132 | 3 | HG02630.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.35-14565_35-14564d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33592374 | |||||
| chr20:33592382
|
A | ATATATAT others(16): Show |
23 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(20): Show | 23 | HG00099.hp1 HG01074.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.35-14542_35-14520d others(25): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33592382 | |||||
| chr20:33592382
|
A | ATATATAT others(18): Show |
6 | a0001c0001t0003g0087a0001c0001t0005g0079a0001c0001t0008g0002others(3): Show | 6 | HG01261.hp2 HG02895.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-14564_35-14563i others(27): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33592382 | |||||
| chr20:33592528
|
T | C | 1 | a0004c0007t0002g0055 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.35-14428T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33592528 | ||||||
| chr20:33592672
|
G | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-14284G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33592672 | ||||||
| chr20:33592689
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.35-14267C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33592689 | ||||||
| chr20:33592741
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.35-14215A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33592741 | ||||||
| chr20:33592882
|
A | G | 1 | a0001c0001t0003g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.35-14074A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33592882 | ||||||
| chr20:33593377
|
A | G | 3 | a0001c0002t0002g0287a0001c0002t0002g0288a0001c0002t0009g0290 | 3 | NA18944.hp1 NA19056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.35-13579A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33593377 | ||||||
| chr20:33593391
|
A | AT | 22 | a0001c0001t0001g0195a0001c0001t0013g0197a0001c0001t0020g0160others(19): Show | 22 | HG00438.hp2 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.35-13543dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33593391 | |||||
| chr20:33593391
|
A | ATT | 43 | a0001c0001t0001g0159a0001c0001t0001g0224a0001c0001t0001g0225others(40): Show | 43 | HG00621.hp2 HG01106.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.35-13544_35-13543d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33593391 | |||||
| chr20:33593391
|
A | ATTT | 21 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0001t0001g0223others(18): Show | 21 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.35-13545_35-13543d others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33593391 | |||||
| chr20:33593391
|
AT | A | 96 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(93): Show | 96 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.35-13543delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33593391 | |||||
| chr20:33593391
|
ATT | A | 37 | a0001c0001t0003g0111a0001c0001t0004g0017a0001c0001t0004g0019others(34): Show | 37 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.35-13544_35-13543d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33593391 | |||||
| chr20:33593593
|
A | G | 1 | a0001c0001t0004g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.35-13363A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33593593 | ||||||
| chr20:33593683
|
A | G | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.35-13273A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33593683 | ||||||
| chr20:33593787
|
A | AAG | 215 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(212): Show | 215 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.35-13166_35-13165d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33593787 | |||||
| chr20:33593819
|
T | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-13137T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33593819 | ||||||
| chr20:33593879
|
C | A | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.35-13077C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33593879 | ||||||
| chr20:33593934
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.35-13022G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33593934 | ||||||
| chr20:33594023
|
G | A | 1 | a0001c0001t0040g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.35-12933G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594023 | ||||||
| chr20:33594075
|
A | C | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.35-12881A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594075 | ||||||
| chr20:33594148
|
G | A | 48 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(45): Show | 48 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.35-12808G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594148 | ||||||
| chr20:33594198
|
T | C | 1 | a0001c0002t0002g0035 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.35-12758T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594198 | ||||||
| chr20:33594322
|
A | C | 1 | a0001c0002t0002g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.35-12634A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594322 | ||||||
| chr20:33594326
|
A | C | 16 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(13): Show | 16 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.35-12630A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594326 | ||||||
| chr20:33594346
|
C | T | 1 | a0001c0001t0012g0163 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.35-12610C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594346 | ||||||
| chr20:33594442
|
G | C | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.35-12514G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594442 | ||||||
| chr20:33594456
|
G | A | 67 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(64): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.35-12500G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594456 | ||||||
| chr20:33594517
|
G | T | 3 | a0001c0002t0002g0196a0001c0002t0002g0206a0001c0002t0002g0211 | 3 | HG01891.hp1 HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.35-12439G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594517 | ||||||
| chr20:33594555
|
G | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-12401G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594555 | ||||||
| chr20:33594655
|
G | A | 14 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(11): Show | 14 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.35-12301G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594655 | ||||||
| chr20:33594666
|
T | C | 3 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0013 | 3 | HG02145.hp2 HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.35-12290T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594666 | ||||||
| chr20:33594689
|
T | C | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.35-12267T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594689 | ||||||
| chr20:33594760
|
G | C | 1 | a0001c0002t0027g0213 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.35-12196G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594760 | ||||||
| chr20:33594765
|
C | T | 4 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-12191C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594765 | ||||||
| chr20:33594893
|
G | T | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.35-12063G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594893 | ||||||
| chr20:33594931
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-12025C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33594931 | ||||||
| chr20:33595086
|
A | G | 3 | a0001c0002t0002g0169a0001c0002t0002g0171a0001c0002t0002g0200 | 3 | HG00438.hp2 HG02155.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.35-11870A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595086 | ||||||
| chr20:33595127
|
G | A | 1 | a0001c0001t0006g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.35-11829G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595127 | ||||||
| chr20:33595144
|
C | T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-11812C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595144 | ||||||
| chr20:33595173
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-11783G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595173 | ||||||
| chr20:33595201
|
T | C | 6 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-11755T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595201 | ||||||
| chr20:33595220
|
T | A | 15 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(12): Show | 15 | HG00738.hp1 HG01261.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.35-11736T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595220 | ||||||
| chr20:33595221
|
T | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.35-11735T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595221 | ||||||
| chr20:33595238
|
G | A | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.35-11718G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595238 | ||||||
| chr20:33595242
|
C | T | 6 | a0001c0002t0002g0031a0001c0002t0002g0046a0001c0002t0002g0053others(3): Show | 6 | HG02135.hp2 NA18943.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-11714C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595242 | ||||||
| chr20:33595400
|
C | T | 1 | a0001c0002t0002g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.35-11556C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595400 | ||||||
| chr20:33595473
|
G | A | 1 | a0001c0002t0002g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.35-11483G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595473 | ||||||
| chr20:33595575
|
C | T | 4 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0006others(1): Show | 4 | HG01261.hp2 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-11381C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595575 | ||||||
| chr20:33595621
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.35-11335G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595621 | ||||||
| chr20:33595800
|
A | G | 4 | a0001c0001t0013g0197a0001c0001t0013g0199a0001c0001t0013g0212others(1): Show | 4 | HG02622.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-11156A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33595800 | ||||||
| chr20:33596050
|
T | C | 1 | a0001c0002t0002g0187 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.35-10906T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33596050 | ||||||
| chr20:33596200
|
C | G | 54 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(51): Show | 54 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.35-10756C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33596200 | ||||||
| chr20:33596215
|
G | A | 2 | a0001c0001t0018g0120a0001c0001t0018g0121 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.35-10741G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33596215 | ||||||
| chr20:33596239
|
CAGTTA | C | 14 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(11): Show | 14 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.35-10712_35-10708d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33596239 | |||||
| chr20:33596398
|
A | T | 1 | a0001c0002t0002g0206 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.35-10558A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33596398 | ||||||
| chr20:33596613
|
G | A | 2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.35-10343G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33596613 | ||||||
| chr20:33596716
|
C | G | 68 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(65): Show | 68 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.35-10240C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33596716 | ||||||
| chr20:33596720
|
A | G | 1 | a0001c0001t0010g0088 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.35-10236A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33596720 | ||||||
| chr20:33596746
|
C | T | 1 | a0001c0002t0017g0124 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.35-10210C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33596746 | ||||||
| chr20:33596864
|
A | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0280 | 2 | NA18960.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.35-10092A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33596864 | ||||||
| chr20:33596919
|
G | GT | 28 | a0001c0001t0001g0267a0001c0001t0004g0029a0001c0001t0004g0030others(25): Show | 28 | HG00438.hp1 HG00639.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.35-10019dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33596919 | |||||
| chr20:33596919
|
GT | G | 104 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(101): Show | 104 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.35-10019delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33596919 | |||||
| chr20:33596934
|
T | C | 5 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-10022T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33596934 | ||||||
| chr20:33597120
|
C | T | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.35-9836C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33597120 | ||||||
| chr20:33597378
|
T | C | 8 | a0001c0001t0005g0079a0001c0001t0005g0080a0001c0001t0005g0081others(5): Show | 8 | HG01243.hp2 HG02145.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.35-9578T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33597378 | ||||||
| chr20:33597482
|
A | G | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.35-9474A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33597482 | ||||||
| chr20:33597743
|
C | T | 3 | a0001c0002t0016g0170a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.35-9213C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33597743 | ||||||
| chr20:33597839
|
C | T | 3 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0013 | 3 | HG02145.hp2 HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.35-9117C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33597839 | ||||||
| chr20:33597855
|
A | G | 1 | a0001c0001t0004g0023 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.35-9101A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33597855 | ||||||
| chr20:33597895
|
C | G | 1 | a0001c0001t0001g0268 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.35-9061C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33597895 | ||||||
| chr20:33598184
|
G | A | 1 | a0001c0002t0045g0216 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.35-8772G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33598184 | ||||||
| chr20:33598465
|
T | C | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-8491T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33598465 | ||||||
| chr20:33598486
|
A | C | 1 | a0001c0001t0006g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.35-8470A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33598486 | ||||||
| chr20:33598491
|
C | T | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.35-8465C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33598491 | ||||||
| chr20:33598676
|
A | C | 1 | a0001c0001t0010g0150 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.35-8280A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33598676 | ||||||
| chr20:33599058
|
C | T | 14 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.35-7898C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33599058 | ||||||
| chr20:33599240
|
C | T | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.35-7716C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33599240 | ||||||
| chr20:33599262
|
G | A | 219 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(216): Show | 219 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.35-7694G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33599262 | ||||||
| chr20:33599302
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.35-7654A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33599302 | ||||||
| chr20:33599588
|
C | CT | 8 | a0001c0001t0005g0078a0001c0001t0005g0084a0001c0001t0005g0085others(5): Show | 8 | HG02559.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.35-7354dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33599588 | |||||
| chr20:33599588
|
CT | C | 6 | a0001c0001t0001g0250a0001c0001t0014g0184a0001c0001t0031g0068others(3): Show | 6 | HG02630.hp2 HG03491.hp2 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-7354delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33599588 | |||||
| chr20:33599641
|
A | G | 67 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(64): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.35-7315A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33599641 | ||||||
| chr20:33599809
|
G | A | 67 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(64): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.35-7147G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33599809 | ||||||
| chr20:33599813
|
T | G | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-7143T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33599813 | ||||||
| chr20:33600087
|
A | C | 1 | a0001c0001t0010g0150 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.35-6869A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33600087 | ||||||
| chr20:33600101
|
C | T | 1 | a0001c0001t0026g0198 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.35-6855C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33600101 | ||||||
| chr20:33600169
|
T | C | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.35-6787T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33600169 | ||||||
| chr20:33600182
|
G | GT | 131 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(128): Show | 131 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.35-6745dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33600182 | |||||
| chr20:33600182
|
G | GTT | 36 | a0001c0001t0001g0223a0001c0001t0001g0228a0001c0001t0001g0237others(33): Show | 36 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.35-6746_35-6745dup others(2): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33600182 | |||||
| chr20:33600184
|
T | TG | 7 | a0001c0002t0002g0178a0001c0002t0002g0180a0001c0002t0016g0170others(4): Show | 7 | HG01123.hp1 HG01255.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.35-6772_35-6771ins others(1): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33600184 | ||||||
| chr20:33600262
|
A | T | 85 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.35-6694A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33600262 | ||||||
| chr20:33600336
|
C | T | 12 | a0001c0001t0003g0089a0001c0001t0003g0090a0001c0001t0003g0109others(9): Show | 12 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.35-6620C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33600336 | ||||||
| chr20:33600376
|
T | G | 3 | a0001c0001t0006g0094a0001c0001t0006g0095a0001c0001t0006g0144 | 3 | HG00408.hp2 HG00544.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.35-6580T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33600376 | ||||||
| chr20:33600886
|
A | C | 1 | a0001c0001t0007g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.35-6070A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33600886 | ||||||
| chr20:33601156
|
C | T | 67 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(64): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.35-5800C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33601156 | ||||||
| chr20:33601508
|
G | A | 1 | a0001c0003t0001g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.35-5448G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33601508 | ||||||
| chr20:33601512
|
G | A | 1 | a0001c0001t0006g0144 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.35-5444G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33601512 | ||||||
| chr20:33601607
|
C | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-5349C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33601607 | ||||||
| chr20:33601782
|
A | C | 3 | a0001c0001t0019g0082a0001c0001t0019g0117a0001c0001t0038g0116 | 3 | NA18939.hp2 NA18971.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.35-5174A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33601782 | ||||||
| chr20:33601809
|
A | AT | 222 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(219): Show | 222 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.35-5134dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33601809 | |||||
| chr20:33601868
|
G | A | 1 | a0001c0001t0010g0075 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.35-5088G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33601868 | ||||||
| chr20:33601953
|
C | T | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.35-5003C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33601953 | ||||||
| chr20:33601989
|
G | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.35-4967G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33601989 | ||||||
| chr20:33602437
|
T | TA | 16 | a0001c0001t0005g0078a0001c0001t0005g0079a0001c0001t0005g0080others(13): Show | 16 | HG01243.hp2 HG02145.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.35-4503dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33602437 | |||||
| chr20:33602437
|
TA | T | 55 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(52): Show | 55 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.35-4503delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33602437 | |||||
| chr20:33602652
|
T | C | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.35-4304T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33602652 | ||||||
| chr20:33602801
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.35-4155G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33602801 | ||||||
| chr20:33602955
|
G | A | 3 | a0001c0004t0006g0140a0001c0004t0006g0142a0001c0004t0044g0092 | 3 | HG01123.hp2 HG02109.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.35-4001G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33602955 | ||||||
| chr20:33603054
|
T | C | 4 | a0001c0001t0006g0094a0001c0001t0006g0095a0001c0001t0006g0118others(1): Show | 4 | HG00408.hp2 HG00544.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-3902T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33603054 | ||||||
| chr20:33603124
|
G | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-3832G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33603124 | ||||||
| chr20:33603417
|
A | G | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.35-3539A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33603417 | ||||||
| chr20:33603723
|
A | G | 3 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0028 | 3 | HG02615.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.35-3233A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33603723 | ||||||
| chr20:33604044
|
C | T | 4 | a0001c0001t0006g0094a0001c0001t0006g0095a0001c0001t0006g0118others(1): Show | 4 | HG00408.hp2 HG00544.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-2912C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33604044 | ||||||
| chr20:33604354
|
C | G | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.35-2602C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33604354 | ||||||
| chr20:33604463
|
C | G | 4 | a0001c0001t0001g0159a0001c0001t0001g0241a0001c0001t0001g0246others(1): Show | 4 | HG02132.hp2 HG02523.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-2493C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33604463 | ||||||
| chr20:33604581
|
C | G | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.35-2375C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33604581 | ||||||
| chr20:33604723
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-2233A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33604723 | ||||||
| chr20:33604847
|
G | A | 1 | a0001c0002t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.35-2109G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33604847 | ||||||
| chr20:33605206
|
G | T | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.35-1750G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33605206 | ||||||
| chr20:33605305
|
T | C | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-1651T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33605305 | ||||||
| chr20:33605732
|
A | G | 1 | a0001c0004t0006g0093 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.35-1224A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33605732 | ||||||
| chr20:33605797
|
A | G | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-1159A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33605797 | ||||||
| chr20:33605825
|
A | AT | 17 | a0001c0001t0006g0083a0001c0001t0006g0091a0001c0001t0006g0094others(14): Show | 17 | HG00408.hp2 HG00544.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.35-1118dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33605825 | |||||
| chr20:33605825
|
AT | A | 9 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(6): Show | 9 | HG00438.hp2 HG02155.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.35-1118delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr20 | 33605825 | |||||
| chr20:33605899
|
A | G | 1 | a0001c0001t0022g0103 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.35-1057A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33605899 | ||||||
| chr20:33605904
|
C | T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.35-1052C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33605904 | ||||||
| chr20:33605992
|
T | C | 1 | a0001c0001t0003g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.35-964T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33605992 | ||||||
| chr20:33606118
|
C | G | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.35-838C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33606118 | ||||||
| chr20:33606166
|
T | C | 3 | a0001c0001t0004g0025a0001c0001t0004g0026a0001c0001t0004g0028 | 3 | HG02615.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.35-790T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33606166 | ||||||
| chr20:33606178
|
C | G | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.35-778C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33606178 | ||||||
| chr20:33606208
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.35-748T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33606208 | ||||||
| chr20:33606244
|
G | T | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.35-712G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33606244 | ||||||
| chr20:33606444
|
A | C | 2 | a0001c0001t0018g0120a0001c0001t0018g0121 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.35-512A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33606444 | ||||||
| chr20:33606445
|
A | T | 2 | a0001c0001t0018g0120a0001c0001t0018g0121 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.35-511A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33606445 | ||||||
| chr20:33606491
|
G | A | 2 | a0001c0001t0003g0115a0001c0001t0003g0158 | 2 | HG01074.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.35-465G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33606491 | ||||||
| chr20:33606599
|
T | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.35-357T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33606599 | ||||||
| chr20:33606601
|
G | A | 5 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016others(2): Show | 5 | HG02559.hp1 HG02630.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-355G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 1/10 | chr20 | 33606601 | ||||||
| chr20:33607797
|
C | A | 57 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(54): Show | 57 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.178+698C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33607797 | ||||||
| chr20:33607939
|
A | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178+840A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33607939 | ||||||
| chr20:33607945
|
C | T | 16 | a0001c0001t0006g0083a0001c0001t0006g0091a0001c0001t0006g0094others(13): Show | 16 | HG00408.hp2 HG00544.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.178+846C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33607945 | ||||||
| chr20:33608060
|
A | G | 2 | a0001c0001t0031g0068a0001c0001t0032g0070 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.178+961A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33608060 | ||||||
| chr20:33608102
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.178+1003C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33608102 | ||||||
| chr20:33608542
|
A | C | 1 | a0001c0001t0006g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.178+1443A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33608542 | ||||||
| chr20:33608862
|
G | A | 1 | a0001c0001t0004g0051 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.178+1763G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33608862 | ||||||
| chr20:33609141
|
C | G | 4 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-1953C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33609141 | ||||||
| chr20:33609166
|
TTAA | T | 4 | a0001c0001t0005g0084a0001c0001t0005g0085a0001c0001t0005g0086others(1): Show | 4 | HG02647.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-1924_179-1922d others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr20 | 33609166 | |||||
| chr20:33609201
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.179-1893T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33609201 | ||||||
| chr20:33609233
|
G | C | 7 | a0001c0001t0004g0027a0001c0001t0007g0067a0001c0001t0007g0069others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-1861G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33609233 | ||||||
| chr20:33609305
|
A | G | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.179-1789A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33609305 | ||||||
| chr20:33609314
|
A | G | 3 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022 | 3 | HG00738.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.179-1780A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33609314 | ||||||
| chr20:33609339
|
A | G | 1 | a0001c0002t0002g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.179-1755A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33609339 | ||||||
| chr20:33609405
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.179-1689G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33609405 | ||||||
| chr20:33609581
|
C | T | 1 | a0001c0001t0007g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.179-1513C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33609581 | ||||||
| chr20:33609980
|
G | A | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.179-1114G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33609980 | ||||||
| chr20:33610567
|
A | G | 1 | a0001c0002t0002g0204 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.179-527A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33610567 | ||||||
| chr20:33610747
|
GTATCCCA others(12): Show |
G | 1 | a0001c0004t0044g0092 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.179-345_179-327del others(19): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr20 | 33610747 | |||||
| chr20:33610800
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.179-294G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33610800 | ||||||
| chr20:33611060
|
G | A | 2 | a0001c0002t0002g0288a0001c0002t0009g0290 | 2 | NA19056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.179-34G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 2/10 | chr20 | 33611060 | ||||||
| chr20:33611393
|
C | T | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.420+58C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33611393 | ||||||
| chr20:33611767
|
G | A | 1 | a0001c0001t0040g0295 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.420+432G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33611767 | ||||||
| chr20:33611804
|
A | G | 1 | a0001c0001t0006g0157 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.420+469A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33611804 | ||||||
| chr20:33611826
|
C | T | 4 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+491C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33611826 | ||||||
| chr20:33612066
|
G | A | 219 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(216): Show | 219 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.420+731G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33612066 | ||||||
| chr20:33612217
|
G | A | 2 | a0001c0002t0002g0183a0001c0002t0002g0201 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.420+882G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33612217 | ||||||
| chr20:33612232
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.420+897C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33612232 | ||||||
| chr20:33612534
|
GTATGCTA others(21): Show |
G | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.420+1223_420+1250d others(30): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33612534 | |||||
| chr20:33612619
|
G | A | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.420+1284G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33612619 | ||||||
| chr20:33612760
|
T | C | 2 | a0001c0002t0002g0046a0002c0008t0002g0047 | 2 | HG02135.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.420+1425T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33612760 | ||||||
| chr20:33612817
|
A | G | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.420+1482A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33612817 | ||||||
| chr20:33612914
|
C | T | 1 | a0001c0002t0002g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.420+1579C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33612914 | ||||||
| chr20:33612986
|
T | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.420+1651T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33612986 | ||||||
| chr20:33613031
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.420+1696C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33613031 | ||||||
| chr20:33613064
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0280 | 2 | NA18960.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.420+1729C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33613064 | ||||||
| chr20:33613508
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.420+2173A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33613508 | ||||||
| chr20:33613601
|
A | C | 2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.420+2266A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33613601 | ||||||
| chr20:33613664
|
C | T | 1 | a0001c0001t0003g0149 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.420+2329C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33613664 | ||||||
| chr20:33613665
|
C | G | 1 | a0001c0001t0005g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.420+2330C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33613665 | ||||||
| chr20:33613676
|
C | T | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.420+2341C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33613676 | ||||||
| chr20:33613700
|
C | T | 1 | a0001c0003t0001g0233 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.420+2365C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33613700 | ||||||
| chr20:33613959
|
C | T | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.420+2624C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33613959 | ||||||
| chr20:33614040
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.420+2705C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33614040 | ||||||
| chr20:33614057
|
G | T | 1 | a0001c0001t0004g0037 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.420+2722G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33614057 | ||||||
| chr20:33614114
|
C | CA | 17 | a0001c0001t0001g0249a0001c0001t0005g0136a0001c0001t0007g0008others(14): Show | 17 | HG01175.hp1 HG01261.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+2795dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33614114 | |||||
| chr20:33614114
|
CA | C | 20 | a0001c0001t0004g0019a0001c0001t0004g0024a0001c0001t0004g0029others(17): Show | 20 | HG00438.hp1 HG01361.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.420+2795delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33614114 | |||||
| chr20:33614485
|
A | C | 4 | a0001c0001t0006g0094a0001c0001t0006g0095a0001c0001t0006g0118others(1): Show | 4 | HG00408.hp2 HG00544.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+3150A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33614485 | ||||||
| chr20:33614973
|
C | T | 67 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(64): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.420+3638C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33614973 | ||||||
| chr20:33615007
|
C | G | 1 | a0001c0001t0001g0256 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.420+3672C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33615007 | ||||||
| chr20:33615015
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.420+3680C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33615015 | ||||||
| chr20:33615116
|
T | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.420+3781T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33615116 | ||||||
| chr20:33615521
|
G | A | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.421-3996G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33615521 | ||||||
| chr20:33615557
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG02300.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.421-3960G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33615557 | ||||||
| chr20:33615582
|
C | T | 1 | a0001c0001t0004g0017 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.421-3935C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33615582 | ||||||
| chr20:33615633
|
A | G | 1 | a0001c0001t0004g0040 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.421-3884A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33615633 | ||||||
| chr20:33615833
|
C | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.421-3684C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33615833 | ||||||
| chr20:33616078
|
G | GAGAT | 43 | a0001c0001t0001g0222a0001c0001t0001g0237a0001c0001t0001g0240others(40): Show | 43 | HG00544.hp1 HG00639.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.421-3386_421-3383d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616078 | |||||
| chr20:33616078
|
G | GAGATAGA others(1): Show |
13 | a0001c0001t0001g0195a0001c0001t0001g0225a0001c0001t0001g0244others(10): Show | 13 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.421-3390_421-3383d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616078 | |||||
| chr20:33616078
|
G | GAGATAGA others(5): Show |
4 | a0001c0002t0002g0034a0001c0002t0002g0044a0001c0002t0002g0059others(1): Show | 4 | HG02080.hp1 NA18747.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.421-3394_421-3383d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616078 | |||||
| chr20:33616078
|
G | GAGATAGA others(9): Show |
1 | a0001c0002t0002g0033 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.421-3398_421-3383d others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616078 | |||||
| chr20:33616078
|
GAGAT | G | 55 | a0001c0001t0001g0224a0001c0001t0001g0238a0001c0001t0001g0241others(52): Show | 55 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.421-3386_421-3383d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616078 | |||||
| chr20:33616078
|
GAGATAGA others(1): Show |
G | 26 | a0001c0001t0001g0236a0001c0001t0001g0246a0001c0001t0001g0259others(23): Show | 26 | HG00323.hp2 HG00408.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.421-3390_421-3383d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616078 | |||||
| chr20:33616078
|
GAGATAGA others(5): Show |
G | 3 | a0001c0001t0004g0030a0001c0002t0002g0177a0001c0010t0028g0132 | 3 | HG00099.hp1 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.421-3394_421-3383d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616078 | |||||
| chr20:33616078
|
GAGATAGA others(9): Show |
G | 2 | a0001c0001t0004g0039a0001c0001t0004g0058 | 2 | HG01496.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.421-3398_421-3383d others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616078 | |||||
| chr20:33616078
|
GAGATAGA others(13): Show |
G | 13 | a0001c0001t0003g0109a0001c0001t0004g0037a0001c0001t0004g0038others(10): Show | 13 | HG00438.hp1 HG01070.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.421-3402_421-3383d others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616078 | |||||
| chr20:33616078
|
GAGATAGA others(17): Show |
G | 1 | a0001c0002t0002g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.421-3406_421-3383d others(26): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616078 | |||||
| chr20:33616165
|
A | T | 1 | a0001c0001t0003g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.421-3352A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33616165 | ||||||
| chr20:33616508
|
CTTGAGGT others(6): Show |
C | 1 | a0001c0001t0004g0061 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.421-3005_421-2993d others(15): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616508 | |||||
| chr20:33616602
|
C | T | 1 | a0001c0001t0007g0012 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.421-2915C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33616602 | ||||||
| chr20:33616669
|
G | C | 2 | a0001c0001t0001g0195a0001c0001t0042g0194 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.421-2848G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33616669 | ||||||
| chr20:33616726
|
CA | C | 17 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(14): Show | 17 | HG01261.hp2 HG01884.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-2777delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33616726 | |||||
| chr20:33617194
|
A | G | 7 | a0001c0001t0003g0101a0001c0001t0003g0104a0001c0001t0003g0105others(4): Show | 7 | HG00408.hp1 HG02080.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-2323A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33617194 | ||||||
| chr20:33617217
|
G | C | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.421-2300G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33617217 | ||||||
| chr20:33617235
|
G | GA | 46 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(43): Show | 46 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.421-2271dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33617235 | |||||
| chr20:33617247
|
T | A | 1 | a0001c0002t0002g0284 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.421-2270T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33617247 | ||||||
| chr20:33617330
|
T | G | 1 | a0001c0001t0004g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.421-2187T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33617330 | ||||||
| chr20:33617351
|
A | G | 1 | a0001c0002t0002g0201 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.421-2166A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33617351 | ||||||
| chr20:33617419
|
T | G | 4 | a0001c0001t0006g0094a0001c0001t0006g0095a0001c0001t0006g0118others(1): Show | 4 | HG00408.hp2 HG00544.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-2098T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33617419 | ||||||
| chr20:33617687
|
T | C | 2 | a0001c0001t0018g0120a0001c0001t0018g0121 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.421-1830T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33617687 | ||||||
| chr20:33617971
|
T | A | 1 | a0001c0001t0010g0151 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.421-1546T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33617971 | ||||||
| chr20:33618095
|
C | G | 2 | a0001c0001t0003g0089a0001c0001t0010g0114 | 2 | HG00323.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.421-1422C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33618095 | ||||||
| chr20:33618155
|
G | A | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.421-1362G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33618155 | ||||||
| chr20:33618164
|
T | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.421-1353T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33618164 | ||||||
| chr20:33618173
|
C | CT | 89 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(86): Show | 89 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.421-1329dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33618173 | |||||
| chr20:33618173
|
CT | C | 36 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(33): Show | 36 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.421-1329delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33618173 | |||||
| chr20:33618275
|
A | G | 1 | a0001c0002t0002g0284 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.421-1242A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33618275 | ||||||
| chr20:33618361
|
T | G | 3 | a0001c0001t0021g0265a0001c0001t0021g0278a0001c0001t0043g0221 | 3 | HG02735.hp1 HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.421-1156T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33618361 | ||||||
| chr20:33618551
|
G | T | 1 | a0001c0001t0005g0138 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.421-966G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33618551 | ||||||
| chr20:33618641
|
T | G | 1 | a0001c0001t0003g0122 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.421-876T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33618641 | ||||||
| chr20:33618641
|
TTTTGTTT others(1): Show |
T | 30 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(27): Show | 30 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.421-851_421-844del others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33618641 | |||||
| chr20:33618783
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.421-734G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33618783 | ||||||
| chr20:33618860
|
A | G | 2 | a0001c0001t0037g0296a0001c0001t0040g0295 | 2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.421-657A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33618860 | ||||||
| chr20:33618933
|
G | T | 1 | a0001c0001t0015g0015 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.421-584G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33618933 | ||||||
| chr20:33619102
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.421-415C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33619102 | ||||||
| chr20:33619127
|
C | G | 2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.421-390C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33619127 | ||||||
| chr20:33619246
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.421-271G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33619246 | ||||||
| chr20:33619262
|
G | A | 7 | a0001c0001t0004g0027a0001c0001t0007g0067a0001c0001t0007g0069others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.421-255G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33619262 | ||||||
| chr20:33619348
|
A | G | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.421-169A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33619348 | ||||||
| chr20:33619406
|
CAAAT | C | 28 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(25): Show | 28 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.421-92_421-89delAT others(2): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33619406 | |||||
| chr20:33619428
|
A | G | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.421-89A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | chr20 | 33619428 | ||||||
| chr20:33619432
|
TA | T | 9 | a0001c0001t0001g0272a0001c0001t0010g0151a0001c0001t0013g0197others(6): Show | 9 | HG02080.hp2 HG02622.hp2 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.421-70delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr20 | 33619432 | |||||
| chr20:33619691
|
C | T | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.510+85C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33619691 | ||||||
| chr20:33620103
|
A | G | 1 | a0001c0002t0002g0060 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.510+497A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33620103 | ||||||
| chr20:33620459
|
T | C | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.510+853T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33620459 | ||||||
| chr20:33620562
|
G | A | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.510+956G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33620562 | ||||||
| chr20:33620895
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510+1289G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33620895 | ||||||
| chr20:33621067
|
C | T | 1 | a0001c0001t0014g0032 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.510+1461C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33621067 | ||||||
| chr20:33621150
|
C | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.510+1544C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33621150 | ||||||
| chr20:33621187
|
CTGTATTC others(101): Show |
C | 1 | a0001c0003t0001g0266 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.510+1583_510+1690d others(2): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621187 | |||||
| chr20:33621192
|
T | TTCAATTG others(20): Show |
1 | a0001c0001t0001g0241 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.510+1592_510+1618d others(29): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621192 | |||||
| chr20:33621287
|
C | CT | 30 | a0001c0001t0001g0261a0001c0001t0001g0280a0001c0001t0004g0019others(27): Show | 30 | HG00438.hp1 HG00741.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.510+1707dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTT | 9 | a0001c0001t0001g0248a0001c0001t0004g0027a0001c0002t0002g0033others(6): Show | 9 | HG00438.hp2 HG01109.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+1706_510+1707d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTT | 7 | a0001c0001t0001g0235a0001c0001t0008g0002a0001c0001t0008g0006others(4): Show | 7 | HG00597.hp1 HG00741.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+1705_510+1707d others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0269a0001c0001t0018g0120a0001c0001t0037g0296others(1): Show | 4 | HG00544.hp2 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+1698_510+1707d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0249 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.510+1697_510+1707d others(13): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.510+1696_510+1707d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(8): Show |
4 | a0001c0001t0013g0197a0001c0001t0013g0199a0001c0001t0013g0212others(1): Show | 4 | HG02622.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+1693_510+1707d others(17): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(13): Show |
4 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0013others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+1688_510+1707d others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0001g0195a0001c0001t0001g0236 | 2 | HG02280.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.510+1687_510+1707d others(23): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0001g0253a0001c0001t0001g0270 | 2 | HG00735.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.510+1686_510+1707d others(24): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(16): Show |
5 | a0001c0001t0001g0228a0001c0001t0001g0234a0001c0001t0001g0239others(2): Show | 5 | NA18965.hp1 NA18982.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+1685_510+1707d others(25): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(17): Show |
9 | a0001c0001t0001g0225a0001c0001t0001g0240a0001c0001t0001g0247others(6): Show | 9 | HG01243.hp1 HG01261.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+1684_510+1707d others(26): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(18): Show |
4 | a0001c0001t0001g0159a0001c0001t0001g0274a0001c0001t0021g0278others(1): Show | 4 | HG00621.hp2 HG03688.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+1683_510+1707d others(27): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(19): Show |
3 | a0001c0001t0001g0238a0001c0001t0007g0011a0001c0003t0001g0230 | 3 | HG02300.hp2 HG02723.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.510+1682_510+1707d others(28): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(20): Show |
2 | a0001c0001t0001g0258a0001c0001t0001g0268 | 2 | HG02523.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.510+1707_510+1708i others(29): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(21): Show |
6 | a0001c0001t0001g0224a0001c0001t0001g0242a0001c0001t0001g0255others(3): Show | 6 | HG01516.hp1 HG02735.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+1707_510+1708i others(30): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(22): Show |
2 | a0001c0001t0001g0237a0001c0001t0001g0252 | 2 | HG01517.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.510+1707_510+1708i others(31): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(23): Show |
2 | a0001c0001t0001g0272a0001c0001t0043g0221 | 2 | HG03669.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.510+1707_510+1708i others(32): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(24): Show |
3 | a0001c0001t0001g0244a0001c0001t0001g0267a0001c0001t0008g0005 | 3 | HG01106.hp1 HG01175.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.510+1707_510+1708i others(33): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0008g0004 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.510+1707_510+1708i others(34): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(26): Show |
2 | a0001c0001t0001g0251a0001c0001t0001g0254 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.510+1707_510+1708i others(35): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(27): Show |
2 | a0001c0001t0001g0243a0001c0001t0001g0298 | 2 | NA19002.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.510+1707_510+1708i others(36): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0001g0262 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.510+1707_510+1708i others(37): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
C | CTTTTTTT others(30): Show |
1 | a0001c0001t0001g0246 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.510+1707_510+1708i others(39): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
CTTTTT | C | 10 | a0001c0001t0007g0067a0001c0001t0011g0062a0001c0001t0011g0063others(7): Show | 10 | HG01167.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.510+1703_510+1707d others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
CTTTTTTT others(1): Show |
C | 45 | a0001c0001t0001g0275a0001c0001t0003g0089a0001c0001t0003g0090others(42): Show | 45 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.510+1700_510+1707d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621287
|
CTTTTTTT others(2): Show |
C | 39 | a0001c0001t0001g0279a0001c0001t0003g0071a0001c0001t0003g0072others(36): Show | 39 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.510+1699_510+1707d others(11): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr20 | 33621287 | |||||
| chr20:33621313
|
T | G | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.510+1707T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33621313 | ||||||
| chr20:33621313
|
T | TTTTTTTT others(22): Show |
1 | a0001c0001t0001g0241 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.510+1707_510+1708i others(31): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33621313 | ||||||
| chr20:33621450
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.511-1665C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33621450 | ||||||
| chr20:33621625
|
C | G | 1 | a0001c0003t0001g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.511-1490C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33621625 | ||||||
| chr20:33622093
|
C | T | 1 | a0001c0002t0009g0290 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.511-1022C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33622093 | ||||||
| chr20:33622432
|
T | G | 85 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.511-683T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33622432 | ||||||
| chr20:33622508
|
G | T | 6 | a0001c0001t0008g0002a0001c0001t0008g0003a0001c0001t0008g0004others(3): Show | 6 | HG01261.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-607G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33622508 | ||||||
| chr20:33622818
|
T | G | 14 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.511-297T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 4/10 | chr20 | 33622818 | ||||||
| chr20:33623337
|
G | A | 57 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(54): Show | 57 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.692+41G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33623337 | ||||||
| chr20:33623362
|
A | T | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.692+66A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33623362 | ||||||
| chr20:33623463
|
G | A | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.692+167G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33623463 | ||||||
| chr20:33623467
|
C | T | 1 | a0001c0001t0004g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.692+171C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33623467 | ||||||
| chr20:33623529
|
A | G | 1 | a0001c0001t0025g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.692+233A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33623529 | ||||||
| chr20:33623540
|
G | A | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.692+244G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33623540 | ||||||
| chr20:33623559
|
A | ATGTT | 50 | a0001c0001t0003g0101a0001c0001t0003g0104a0001c0001t0003g0105others(47): Show | 50 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.692+301_692+304dup others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 33623559 | |||||
| chr20:33623559
|
A | ATGTTTGT others(1): Show |
3 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022 | 3 | HG00738.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.692+297_692+304dup others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 33623559 | |||||
| chr20:33623559
|
ATGTT | A | 111 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(108): Show | 111 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.692+301_692+304del others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 33623559 | |||||
| chr20:33623559
|
ATGTTTGT others(1): Show |
A | 5 | a0001c0001t0001g0258a0001c0001t0004g0019a0001c0001t0010g0150others(2): Show | 5 | HG01981.hp2 HG02523.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.692+297_692+304del others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 33623559 | |||||
| chr20:33623892
|
G | A | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.692+596G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33623892 | ||||||
| chr20:33623953
|
G | A | 35 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(32): Show | 35 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.692+657G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33623953 | ||||||
| chr20:33624142
|
A | G | 1 | a0001c0002t0002g0034 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.693-622A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33624142 | ||||||
| chr20:33624236
|
T | TA | 22 | a0001c0001t0001g0238a0001c0001t0005g0078a0001c0001t0005g0084others(19): Show | 22 | HG01175.hp1 HG01261.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.693-509dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 33624236 | |||||
| chr20:33624236
|
TA | T | 14 | a0001c0001t0001g0251a0001c0001t0001g0256a0001c0001t0003g0107others(11): Show | 14 | HG00741.hp1 HG01256.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.693-509delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 33624236 | |||||
| chr20:33624237
|
A | T | 4 | a0001c0001t0006g0094a0001c0001t0006g0095a0001c0001t0006g0118others(1): Show | 4 | HG00408.hp2 HG00544.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.693-527A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33624237 | ||||||
| chr20:33624251
|
A | G | 1 | a0001c0002t0002g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.693-513A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33624251 | ||||||
| chr20:33624252
|
A | G | 1 | a0001c0001t0010g0075 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.693-512A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33624252 | ||||||
| chr20:33624336
|
T | TA | 37 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(34): Show | 37 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.693-414dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 33624336 | |||||
| chr20:33624336
|
TA | T | 6 | a0001c0001t0001g0236a0001c0001t0003g0100a0001c0001t0005g0084others(3): Show | 6 | HG03209.hp2 HG03579.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.693-414delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr20 | 33624336 | |||||
| chr20:33624353
|
C | T | 2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.693-411C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33624353 | ||||||
| chr20:33624503
|
T | C | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.693-261T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33624503 | ||||||
| chr20:33624534
|
G | T | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.693-230G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33624534 | ||||||
| chr20:33624587
|
A | G | 1 | a0001c0001t0010g0075 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.693-177A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 5/10 | chr20 | 33624587 | ||||||
| chr20:33625359
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.946+342C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33625359 | ||||||
| chr20:33625517
|
A | C | 2 | a0001c0001t0007g0067a0001c0001t0007g0069 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.946+500A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33625517 | ||||||
| chr20:33625589
|
T | A | 13 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(10): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.946+572T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33625589 | ||||||
| chr20:33625679
|
G | A | 2 | a0001c0002t0002g0178a0001c0002t0002g0180 | 2 | HG01123.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.946+662G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33625679 | ||||||
| chr20:33625872
|
G | A | 1 | a0001c0001t0005g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.946+855G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33625872 | ||||||
| chr20:33625875
|
G | T | 1 | a0001c0002t0002g0196 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.946+858G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33625875 | ||||||
| chr20:33625956
|
G | C | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.946+939G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33625956 | ||||||
| chr20:33625977
|
C | T | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.946+960C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33625977 | ||||||
| chr20:33625996
|
G | A | 1 | a0001c0001t0010g0151 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.946+979G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33625996 | ||||||
| chr20:33626255
|
T | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.946+1238T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33626255 | ||||||
| chr20:33626285
|
G | T | 1 | a0001c0002t0002g0201 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.946+1268G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33626285 | ||||||
| chr20:33626396
|
G | A | 7 | a0001c0001t0005g0078a0001c0001t0005g0084a0001c0001t0005g0085others(4): Show | 7 | HG02647.hp2 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.946+1379G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33626396 | ||||||
| chr20:33626526
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.946+1509G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33626526 | ||||||
| chr20:33626757
|
A | G | 1 | a0001c0002t0002g0174 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.947-1593A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33626757 | ||||||
| chr20:33626926
|
C | T | 1 | a0001c0001t0007g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.947-1424C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33626926 | ||||||
| chr20:33626936
|
A | G | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.947-1414A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33626936 | ||||||
| chr20:33626964
|
T | A | 62 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(59): Show | 62 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.947-1386T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33626964 | ||||||
| chr20:33626989
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.947-1361A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33626989 | ||||||
| chr20:33627001
|
A | T | 1 | a0001c0002t0002g0046 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.947-1349A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627001 | ||||||
| chr20:33627177
|
C | T | 2 | a0001c0001t0003g0158a0001c0001t0030g0001 | 2 | HG01074.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.947-1173C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627177 | ||||||
| chr20:33627186
|
A | G | 3 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02559.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.947-1164A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627186 | ||||||
| chr20:33627194
|
G | A | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.947-1156G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627194 | ||||||
| chr20:33627224
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.947-1126C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627224 | ||||||
| chr20:33627225
|
G | A | 1 | a0001c0001t0013g0212 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.947-1125G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627225 | ||||||
| chr20:33627361
|
C | T | 3 | a0001c0001t0003g0096a0001c0001t0003g0145a0001c0001t0003g0153 | 3 | HG02615.hp1 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.947-989C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627361 | ||||||
| chr20:33627390
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.947-960C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627390 | ||||||
| chr20:33627391
|
G | A | 1 | a0001c0001t0003g0127 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.947-959G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627391 | ||||||
| chr20:33627397
|
G | A | 1 | a0001c0002t0002g0196 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.947-953G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627397 | ||||||
| chr20:33627403
|
GA | G | 4 | a0001c0001t0030g0001a0001c0002t0002g0171a0001c0006t0007g0282others(1): Show | 4 | HG02155.hp1 HG02559.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-940delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr20 | 33627403 | |||||
| chr20:33627404
|
A | G | 4 | a0001c0002t0002g0167a0001c0002t0002g0168a0001c0002t0002g0187others(1): Show | 4 | HG00735.hp1 HG01070.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.947-946A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627404 | ||||||
| chr20:33627438
|
A | G | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.947-912A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627438 | ||||||
| chr20:33627680
|
C | T | 1 | a0001c0001t0004g0051 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.947-670C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33627680 | ||||||
| chr20:33628178
|
C | T | 3 | a0001c0002t0016g0193a0001c0002t0024g0074a0001c0002t0035g0202 | 3 | HG01255.hp2 HG02148.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.947-172C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 6/10 | chr20 | 33628178 | ||||||
| chr20:33628592
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1032+157C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 7/10 | chr20 | 33628592 | ||||||
| chr20:33628611
|
G | A | 1 | a0001c0002t0002g0201 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1032+176G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 7/10 | chr20 | 33628611 | ||||||
| chr20:33629429
|
T | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1033-290T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 7/10 | chr20 | 33629429 | ||||||
| chr20:33629557
|
G | A | 2 | a0001c0001t0003g0119a0001c0001t0003g0139 | 2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1033-162G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 7/10 | chr20 | 33629557 | ||||||
| chr20:33629931
|
C | T | 1 | a0001c0001t0020g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1228+17C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33629931 | ||||||
| chr20:33630037
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1228+123A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33630037 | ||||||
| chr20:33630104
|
C | T | 1 | a0001c0002t0002g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1228+190C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33630104 | ||||||
| chr20:33630186
|
A | C | 1 | a0001c0001t0001g0277 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1228+272A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33630186 | ||||||
| chr20:33630266
|
A | T | 1 | a0001c0002t0002g0214 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1228+352A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33630266 | ||||||
| chr20:33630388
|
A | G | 30 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(27): Show | 30 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1228+474A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33630388 | ||||||
| chr20:33630643
|
C | T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1228+729C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33630643 | ||||||
| chr20:33630807
|
T | G | 14 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1228+893T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33630807 | ||||||
| chr20:33631335
|
C | T | 2 | a0001c0002t0002g0189a0001c0002t0002g0208 | 2 | HG00741.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1228+1421C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33631335 | ||||||
| chr20:33631482
|
T | C | 13 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(10): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1228+1568T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33631482 | ||||||
| chr20:33631556
|
C | CTCTTGCT others(13): Show |
5 | a0001c0001t0015g0014a0001c0001t0015g0015a0001c0001t0015g0016others(2): Show | 5 | HG02559.hp1 HG02630.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1228+1659_1228+167 others(24): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33631556 | |||||
| chr20:33631583
|
T | C | 1 | a0001c0005t0002g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1228+1669T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33631583 | ||||||
| chr20:33631608
|
A | G | 1 | a0001c0001t0004g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1228+1694A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33631608 | ||||||
| chr20:33631980
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0264 | 2 | HG02083.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1228+2066C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33631980 | ||||||
| chr20:33632190
|
C | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1228+2276C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33632190 | ||||||
| chr20:33632219
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1228+2305T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33632219 | ||||||
| chr20:33632471
|
C | CT | 28 | a0001c0001t0003g0101a0001c0001t0004g0017a0001c0001t0004g0019others(25): Show | 28 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1228+2574dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33632471 | |||||
| chr20:33632471
|
C | CTTT | 63 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(60): Show | 63 | HG00544.hp2 HG00597.hp1 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.1228+2572_1228+257 others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33632471 | |||||
| chr20:33632801
|
T | C | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1228+2887T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33632801 | ||||||
| chr20:33632954
|
T | A | 1 | a0001c0002t0002g0294 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1228+3040T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33632954 | ||||||
| chr20:33633020
|
A | T | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1228+3106A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33633020 | ||||||
| chr20:33633121
|
C | T | 2 | a0001c0001t0010g0088a0001c0001t0022g0103 | 2 | NA18969.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1228+3207C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33633121 | ||||||
| chr20:33633214
|
CA | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1228+3307delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33633214 | |||||
| chr20:33633304
|
G | A | 6 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1229-3336G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33633304 | ||||||
| chr20:33633363
|
T | A | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1229-3277T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33633363 | ||||||
| chr20:33633370
|
CAAA | C | 10 | a0001c0001t0003g0101a0001c0001t0003g0104a0001c0001t0003g0105others(7): Show | 10 | HG00408.hp1 HG00408.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1229-3262_1229-326 others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33633370 | |||||
| chr20:33633370
|
CAAAA | C | 5 | a0001c0001t0003g0077a0001c0001t0003g0135a0001c0001t0007g0012others(2): Show | 5 | HG01346.hp1 HG02572.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1229-3263_1229-326 others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33633370 | |||||
| chr20:33633377
|
AAAAT | A | 199 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(196): Show | 199 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.1229-3239_1229-323 others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33633377 | |||||
| chr20:33633379
|
AAT | A | 7 | a0001c0001t0004g0027a0001c0001t0007g0067a0001c0001t0007g0069others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1229-3259_1229-325 others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33633379 | |||||
| chr20:33633380
|
AT | A | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1229-3259delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33633380 | ||||||
| chr20:33633385
|
T | A | 33 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(30): Show | 33 | HG00438.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1229-3255T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33633385 | ||||||
| chr20:33633385
|
TAAA | T | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1229-3254_1229-325 others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33633385 | ||||||
| chr20:33633803
|
T | TTGCCATG others(7): Show |
13 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(10): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1229-2835_1229-282 others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33633803 | |||||
| chr20:33633902
|
T | G | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1229-2738T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33633902 | ||||||
| chr20:33633942
|
C | T | 57 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(54): Show | 57 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.1229-2698C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33633942 | ||||||
| chr20:33633961
|
T | G | 52 | a0001c0001t0001g0159a0001c0001t0001g0220a0001c0001t0001g0222others(49): Show | 52 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1229-2679T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33633961 | ||||||
| chr20:33633980
|
T | G | 1 | a0001c0001t0005g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1229-2660T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33633980 | ||||||
| chr20:33634003
|
C | T | 1 | a0001c0001t0013g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1229-2637C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33634003 | ||||||
| chr20:33634018
|
G | A | 1 | a0001c0001t0006g0091 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1229-2622G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33634018 | ||||||
| chr20:33634409
|
C | G | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1229-2231C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33634409 | ||||||
| chr20:33634557
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0280 | 2 | NA18960.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1229-2083G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33634557 | ||||||
| chr20:33634610
|
G | A | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1229-2030G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33634610 | ||||||
| chr20:33634670
|
C | CA | 75 | a0001c0001t0001g0159a0001c0001t0001g0220a0001c0001t0001g0222others(72): Show | 75 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1229-1944dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33634670 | |||||
| chr20:33634670
|
C | CAA | 6 | a0001c0001t0001g0195a0001c0001t0001g0261a0001c0001t0001g0272others(3): Show | 6 | HG01261.hp1 HG02280.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.1229-1945_1229-194 others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33634670 | |||||
| chr20:33634670
|
CA | C | 21 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(18): Show | 21 | HG01167.hp2 HG01361.hp2 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.1229-1944delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33634670 | |||||
| chr20:33634670
|
CAAAAAA | C | 35 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(32): Show | 35 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1229-1949_1229-194 others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33634670 | |||||
| chr20:33634670
|
CAAAAAAA | C | 8 | a0001c0001t0001g0248a0001c0001t0004g0291a0001c0001t0004g0292others(5): Show | 8 | HG02145.hp2 HG02148.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1229-1950_1229-194 others(11): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33634670 | |||||
| chr20:33634670
|
CAAAAAAA others(3): Show |
C | 6 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1229-1953_1229-194 others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33634670 | |||||
| chr20:33634670
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0009g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1229-1954_1229-194 others(15): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33634670 | |||||
| chr20:33634771
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1229-1869G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33634771 | ||||||
| chr20:33634832
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1229-1808C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33634832 | ||||||
| chr20:33635001
|
A | G | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1229-1639A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33635001 | ||||||
| chr20:33635067
|
A | G | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1229-1573A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33635067 | ||||||
| chr20:33635079
|
A | G | 1 | a0001c0002t0002g0181 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1229-1561A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33635079 | ||||||
| chr20:33635193
|
T | C | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1229-1447T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33635193 | ||||||
| chr20:33635234
|
A | G | 85 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(82): Show | 85 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1229-1406A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33635234 | ||||||
| chr20:33635378
|
G | A | 1 | a0001c0001t0005g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1229-1262G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33635378 | ||||||
| chr20:33635463
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1229-1177G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33635463 | ||||||
| chr20:33635480
|
G | C | 3 | a0001c0001t0004g0019a0001c0001t0004g0024a0001c0001t0036g0018 | 3 | HG01361.hp1 NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1229-1160G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33635480 | ||||||
| chr20:33635904
|
A | C | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1229-736A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33635904 | ||||||
| chr20:33635925
|
A | C | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1229-715A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33635925 | ||||||
| chr20:33636036
|
C | T | 1 | a0001c0001t0003g0087 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1229-604C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33636036 | ||||||
| chr20:33636258
|
C | CA | 36 | a0001c0001t0001g0225a0001c0001t0001g0272a0001c0001t0001g0275others(33): Show | 36 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1229-361dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33636258 | |||||
| chr20:33636258
|
CA | C | 38 | a0001c0001t0003g0129a0001c0001t0004g0029a0001c0001t0004g0030others(35): Show | 38 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.1229-361delA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr20 | 33636258 | |||||
| chr20:33636318
|
G | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1229-322G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33636318 | ||||||
| chr20:33636426
|
C | T | 67 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(64): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1229-214C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33636426 | ||||||
| chr20:33636614
|
C | G | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1229-26C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 8/10 | chr20 | 33636614 | ||||||
| chr20:33636958
|
C | T | 1 | a0001c0002t0002g0175 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1297+250C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33636958 | ||||||
| chr20:33636991
|
G | C | 7 | a0001c0002t0002g0166a0001c0002t0002g0177a0001c0002t0002g0203others(4): Show | 7 | HG00099.hp1 HG01074.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1297+283G>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33636991 | ||||||
| chr20:33637087
|
C | T | 1 | a0001c0002t0002g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1297+379C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33637087 | ||||||
| chr20:33637198
|
G | A | 1 | a0001c0001t0003g0089 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1297+490G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33637198 | ||||||
| chr20:33637220
|
G | T | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1297+512G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33637220 | ||||||
| chr20:33637655
|
C | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1297+947C>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33637655 | ||||||
| chr20:33637697
|
C | T | 3 | a0001c0001t0003g0096a0001c0001t0003g0145a0001c0001t0003g0153 | 3 | HG02615.hp1 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1297+989C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33637697 | ||||||
| chr20:33637962
|
C | T | 1 | a0001c0006t0007g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1297+1254C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33637962 | ||||||
| chr20:33637966
|
C | CT | 32 | a0001c0001t0001g0159a0001c0001t0001g0220a0001c0001t0001g0246others(29): Show | 32 | HG00741.hp2 HG01109.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1297+1284dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 33637966 | |||||
| chr20:33637966
|
C | CTTT | 14 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022others(11): Show | 14 | HG00738.hp2 HG01070.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1297+1282_1297+128 others(7): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 33637966 | |||||
| chr20:33637966
|
CT | C | 83 | a0001c0001t0001g0195a0001c0001t0003g0071a0001c0001t0003g0072others(80): Show | 83 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1297+1284delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 33637966 | |||||
| chr20:33637970
|
T | G | 1 | a0001c0002t0009g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1297+1262T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33637970 | ||||||
| chr20:33638115
|
C | T | 2 | a0001c0001t0015g0015a0001c0001t0015g0016 | 2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1297+1407C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33638115 | ||||||
| chr20:33638201
|
T | C | 61 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(58): Show | 61 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.1297+1493T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33638201 | ||||||
| chr20:33638551
|
A | G | 56 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(53): Show | 56 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.1298-1790A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33638551 | ||||||
| chr20:33638562
|
T | A | 1 | a0001c0001t0001g0234 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1298-1779T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33638562 | ||||||
| chr20:33638591
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1298-1750G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33638591 | ||||||
| chr20:33638747
|
G | A | 1 | a0001c0001t0003g0139 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1298-1594G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33638747 | ||||||
| chr20:33638874
|
G | A | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1298-1467G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33638874 | ||||||
| chr20:33639110
|
G | A | 1 | a0001c0001t0004g0023 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1298-1231G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33639110 | ||||||
| chr20:33639116
|
C | T | 2 | a0001c0001t0004g0029a0001c0001t0004g0030 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1298-1225C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33639116 | ||||||
| chr20:33639303
|
G | A | 1 | a0001c0002t0016g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1298-1038G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33639303 | ||||||
| chr20:33639345
|
T | C | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1298-996T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33639345 | ||||||
| chr20:33639448
|
C | G | 1 | a0001c0001t0043g0221 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1298-893C>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33639448 | ||||||
| chr20:33639522
|
A | C | 67 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(64): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1298-819A>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33639522 | ||||||
| chr20:33639573
|
C | CA | 19 | a0001c0001t0004g0029a0001c0001t0004g0030a0001c0001t0004g0037others(16): Show | 19 | HG00438.hp1 HG01070.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.1298-755dupA | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr20 | 33639573 | |||||
| chr20:33639843
|
C | T | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1298-498C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33639843 | ||||||
| chr20:33639864
|
G | A | 1 | a0001c0003t0001g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1298-477G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33639864 | ||||||
| chr20:33639923
|
C | T | 54 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0020others(51): Show | 54 | HG00438.hp1 HG00738.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.1298-418C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33639923 | ||||||
| chr20:33639988
|
G | T | 1 | a0001c0002t0002g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1298-353G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33639988 | ||||||
| chr20:33640107
|
G | A | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1298-234G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33640107 | ||||||
| chr20:33640200
|
T | C | 3 | a0001c0001t0018g0120a0001c0001t0018g0121a0001c0010t0028g0132 | 3 | HG01891.hp2 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1298-141T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33640200 | ||||||
| chr20:33640239
|
G | A | 1 | a0001c0001t0006g0141 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1298-102G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33640239 | ||||||
| chr20:33640250
|
T | C | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1298-91T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33640250 | ||||||
| chr20:33640282
|
C | T | 1 | a0001c0004t0006g0093 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1298-59C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33640282 | ||||||
| chr20:33640309
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1298-32G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 9/10 | chr20 | 33640309 | ||||||
| chr20:33640585
|
G | A | 3 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0010t0028g0132 | 3 | HG02572.hp1 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1488+54G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33640585 | ||||||
| chr20:33640599
|
A | G | 1 | a0001c0002t0002g0033 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1488+68A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33640599 | ||||||
| chr20:33640686
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0042g0194 | 2 | HG02280.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1488+155T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33640686 | ||||||
| chr20:33640726
|
AT | A | 10 | a0001c0001t0003g0077a0001c0001t0003g0087a0001c0001t0003g0097others(7): Show | 10 | HG00597.hp2 HG01346.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1488+197delT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33640726 | |||||
| chr20:33640729
|
G | T | 4 | a0001c0001t0013g0197a0001c0001t0013g0199a0001c0001t0013g0212others(1): Show | 4 | HG02622.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488+198G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33640729 | ||||||
| chr20:33640746
|
C | CAT | 15 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(12): Show | 15 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1488+225_1488+226d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33640746 | |||||
| chr20:33640756
|
T | G | 154 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0222others(151): Show | 154 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1488+225T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33640756 | ||||||
| chr20:33640758
|
G | T | 21 | a0001c0001t0007g0011a0001c0001t0007g0067a0001c0001t0007g0069others(18): Show | 21 | HG00741.hp1 HG01884.hp1 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.1488+227G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33640758 | ||||||
| chr20:33640923
|
A | G | 2 | a0001c0006t0007g0282a0001c0010t0028g0132 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1488+392A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33640923 | ||||||
| chr20:33641267
|
GCACCTAG others(27): Show |
G | 1 | a0001c0001t0017g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1488+737_1488+770d others(36): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33641267 | ||||||
| chr20:33641625
|
C | T | 1 | a0001c0001t0010g0150 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1488+1094C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33641625 | ||||||
| chr20:33641668
|
C | T | 3 | a0001c0001t0014g0293a0001c0001t0018g0120a0001c0001t0018g0121 | 3 | HG01891.hp2 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1488+1137C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33641668 | ||||||
| chr20:33641732
|
A | G | 3 | a0001c0001t0030g0001a0001c0006t0007g0282a0001c0010t0028g0132 | 3 | HG02559.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1488+1201A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33641732 | ||||||
| chr20:33642105
|
C | CT | 6 | a0001c0002t0002g0284a0001c0002t0002g0285a0001c0002t0002g0286others(3): Show | 6 | NA18944.hp1 NA19000.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.1488+1586dupT | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642105 | |||||
| chr20:33642105
|
CTT | C | 6 | a0001c0001t0013g0197a0001c0001t0013g0212a0001c0001t0026g0198others(3): Show | 6 | HG00738.hp1 HG01515.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1488+1585_1488+158 others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642105 | |||||
| chr20:33642105
|
CTTTT | C | 10 | a0001c0001t0004g0027a0001c0001t0004g0041a0001c0001t0004g0042others(7): Show | 10 | HG00438.hp1 HG01109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1488+1583_1488+158 others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642105 | |||||
| chr20:33642105
|
CTTTTTT | C | 14 | a0001c0001t0004g0017a0001c0001t0004g0025a0001c0001t0004g0028others(11): Show | 14 | HG01070.hp2 HG01167.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1488+1581_1488+158 others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642105 | |||||
| chr20:33642105
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022others(6): Show | 9 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1488+1579_1488+158 others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642105 | |||||
| chr20:33642106
|
TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0014g0293 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1488+1577_1488+158 others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642106 | |||||
| chr20:33642108
|
TTTTTTTT others(3): Show |
T | 5 | a0001c0001t0004g0019a0001c0001t0004g0024a0001c0001t0018g0120others(2): Show | 5 | HG01361.hp1 HG01891.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1488+1579_1488+158 others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642108 | |||||
| chr20:33642108
|
TTTTTTTT others(5): Show |
T | 2 | a0001c0001t0015g0015a0003c0009t0029g0283 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1488+1579_1488+159 others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642108 | |||||
| chr20:33642108
|
TTTTTTTT others(7): Show |
T | 7 | a0001c0001t0001g0241a0001c0001t0001g0251a0001c0001t0001g0254others(4): Show | 7 | HG01256.hp1 HG01258.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.1488+1579_1488+159 others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642108 | |||||
| chr20:33642108
|
TTTTTTTT others(9): Show |
T | 6 | a0001c0001t0007g0067a0001c0001t0007g0069a0001c0001t0011g0062others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1488+1579_1488+159 others(20): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642108 | |||||
| chr20:33642108
|
TTTTTTTT others(11): Show |
T | 3 | a0001c0001t0015g0014a0001c0001t0037g0296a0001c0001t0040g0295 | 3 | HG02109.hp2 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1488+1579_1488+159 others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642108 | |||||
| chr20:33642108
|
TTTTTTTT others(15): Show |
T | 13 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(10): Show | 13 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1488+1579_1488+160 others(26): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642108 | |||||
| chr20:33642108
|
TTTTTTTT others(17): Show |
T | 1 | a0001c0010t0028g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1488+1579_1488+160 others(28): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642108 | |||||
| chr20:33642110
|
T | G | 1 | a0001c0001t0004g0058 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1488+1579T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642110 | ||||||
| chr20:33642110
|
T | TTGTGTGT others(7): Show |
1 | a0001c0005t0002g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1488+1580_1488+158 others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642110 | |||||
| chr20:33642110
|
TTTTTTTT others(3): Show |
T | 2 | a0001c0001t0001g0276a0001c0001t0010g0114 | 2 | HG01243.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1488+1581_1488+159 others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642110 | |||||
| chr20:33642110
|
TTTTTTTT others(5): Show |
T | 4 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0021g0265others(1): Show | 4 | HG00558.hp2 HG02273.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1488+1581_1488+159 others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642110 | |||||
| chr20:33642110
|
TTTTTTTT others(7): Show |
T | 50 | a0001c0001t0001g0159a0001c0001t0001g0220a0001c0001t0001g0222others(47): Show | 50 | HG00597.hp1 HG00621.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1488+1581_1488+159 others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642110 | |||||
| chr20:33642110
|
TTTTTTTT others(9): Show |
T | 3 | a0001c0001t0001g0258a0001c0001t0001g0269a0001c0001t0020g0160 | 3 | HG00544.hp2 HG00741.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1488+1581_1488+159 others(20): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642110 | |||||
| chr20:33642110
|
TTTTTTTT others(13): Show |
T | 1 | a0001c0001t0001g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1488+1581_1488+160 others(24): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642110 | |||||
| chr20:33642112
|
T | G | 2 | a0001c0001t0004g0058a0001c0005t0002g0182 | 2 | HG02155.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1488+1581T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642112 | ||||||
| chr20:33642112
|
TTTTTTGT others(3): Show |
T | 3 | a0001c0001t0003g0113a0001c0001t0005g0136a0001c0001t0005g0138 | 3 | HG03098.hp1 HG03516.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1488+1583_1488+159 others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642112 | |||||
| chr20:33642112
|
TTTTTTGT others(5): Show |
T | 14 | a0001c0001t0003g0073a0001c0001t0003g0090a0001c0001t0003g0109others(11): Show | 14 | HG00099.hp2 HG01074.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1488+1583_1488+159 others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642112 | |||||
| chr20:33642112
|
TTTTTTGT others(11): Show |
T | 1 | a0001c0001t0003g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1488+1583_1488+160 others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642112 | |||||
| chr20:33642114
|
T | G | 14 | a0001c0001t0004g0027a0001c0001t0004g0041a0001c0001t0004g0042others(11): Show | 14 | HG00438.hp1 HG01109.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1488+1583T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642114 | ||||||
| chr20:33642114
|
T | TTGTGTGT others(3): Show |
1 | a0001c0005t0002g0179 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1488+1584_1488+158 others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642114 | |||||
| chr20:33642114
|
TTTTGTGT others(3): Show |
T | 9 | a0001c0001t0003g0096a0001c0001t0003g0100a0001c0001t0003g0145others(6): Show | 9 | HG01243.hp2 HG02615.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488+1585_1488+159 others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642114 | |||||
| chr20:33642114
|
TTTTGTGT others(5): Show |
T | 32 | a0001c0001t0003g0077a0001c0001t0003g0087a0001c0001t0003g0089others(29): Show | 32 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1488+1585_1488+159 others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642114 | |||||
| chr20:33642114
|
TTTTGTGT others(7): Show |
T | 2 | a0001c0001t0001g0277a0001c0001t0019g0082 | 2 | HG04199.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1488+1585_1488+159 others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642114 | |||||
| chr20:33642114
|
TTTTGTGT others(9): Show |
T | 1 | a0001c0002t0002g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1488+1585_1488+160 others(20): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642114 | |||||
| chr20:33642116
|
T | G | 38 | a0001c0001t0004g0017a0001c0001t0004g0025a0001c0001t0004g0027others(35): Show | 38 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1488+1585T>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642116 | ||||||
| chr20:33642116
|
T | TG | 3 | a0001c0002t0002g0053a0001c0002t0002g0176a0001c0002t0009g0217 | 3 | HG02683.hp1 HG04184.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1488+1585_1488+158 others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642116 | ||||||
| chr20:33642116
|
TTGTG | T | 9 | a0001c0002t0002g0034a0001c0002t0002g0035a0001c0002t0002g0036others(6): Show | 9 | HG02015.hp2 HG02080.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.1488+1630_1488+163 others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642116 | |||||
| chr20:33642116
|
TTGTGTGT others(3): Show |
T | 3 | a0001c0001t0005g0079a0001c0001t0005g0133a0001c0001t0006g0095 | 3 | HG00544.hp1 HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1488+1624_1488+163 others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642116 | |||||
| chr20:33642116
|
TTGTGTGT others(5): Show |
T | 11 | a0001c0001t0003g0097a0001c0001t0003g0119a0001c0001t0003g0122others(8): Show | 11 | HG00408.hp2 HG00597.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.1488+1622_1488+163 others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33642116 | |||||
| chr20:33642118
|
G | T | 9 | a0001c0002t0002g0046a0001c0002t0002g0171a0001c0002t0002g0178others(6): Show | 9 | HG01256.hp2 HG02135.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488+1587G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642118 | ||||||
| chr20:33642120
|
G | T | 5 | a0001c0001t0017g0102a0001c0002t0002g0046a0001c0002t0002g0185others(2): Show | 5 | HG01256.hp2 HG02135.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1488+1589G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642120 | ||||||
| chr20:33642122
|
G | T | 2 | a0001c0002t0002g0045a0001c0002t0002g0188 | 2 | HG01256.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1488+1591G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642122 | ||||||
| chr20:33642124
|
G | T | 1 | a0001c0002t0002g0045 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1488+1593G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642124 | ||||||
| chr20:33642130
|
G | T | 2 | a0001c0001t0003g0119a0001c0001t0005g0130 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1488+1599G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642130 | ||||||
| chr20:33642165
|
G | T | 2 | a0001c0001t0030g0001a0001c0002t0002g0214 | 2 | HG02738.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1488+1634G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642165 | ||||||
| chr20:33642180
|
C | T | 1 | a0001c0001t0003g0089 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1488+1649C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642180 | ||||||
| chr20:33642510
|
G | T | 12 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0007g0011others(9): Show | 12 | HG01261.hp2 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1489-1837G>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642510 | ||||||
| chr20:33642825
|
C | T | 1 | a0001c0001t0003g0122 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1489-1522C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642825 | ||||||
| chr20:33642998
|
G | A | 1 | a0001c0002t0002g0059 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1489-1349G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33642998 | ||||||
| chr20:33643048
|
C | T | 1 | a0001c0002t0016g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1489-1299C>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643048 | ||||||
| chr20:33643719
|
G | A | 1 | a0001c0001t0003g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1489-628G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643719 | ||||||
| chr20:33643753
|
C | CTA | 9 | a0001c0001t0012g0163a0001c0001t0017g0102a0001c0001t0025g0009others(6): Show | 9 | HG01255.hp2 HG01884.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1489-531_1489-530d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
C | CTATA | 8 | a0001c0002t0002g0035a0001c0002t0002g0046a0001c0002t0002g0177others(5): Show | 8 | HG00099.hp1 HG02015.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.1489-533_1489-530d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
C | CTATATAT others(5): Show |
2 | a0001c0002t0002g0169a0004c0007t0002g0055 | 2 | HG00438.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1489-541_1489-530d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTA | C | 16 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0010g0151others(13): Show | 16 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.1489-531_1489-530d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATA | C | 7 | a0001c0001t0007g0013a0001c0001t0008g0003a0001c0001t0008g0007others(4): Show | 7 | HG01123.hp1 HG02080.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1489-533_1489-530d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATA | C | 6 | a0001c0001t0012g0165a0001c0001t0020g0160a0001c0002t0002g0181others(3): Show | 6 | HG00741.hp1 HG02280.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1489-535_1489-530d others(8): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(1): Show |
C | 7 | a0001c0001t0003g0115a0001c0001t0007g0010a0001c0001t0014g0293others(4): Show | 7 | HG03017.hp2 HG03195.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1489-537_1489-530d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(3): Show |
C | 5 | a0001c0001t0007g0008a0001c0001t0018g0120a0001c0001t0018g0121others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1489-539_1489-530d others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(5): Show |
C | 2 | a0001c0001t0007g0012a0001c0002t0002g0183 | 2 | HG01515.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1489-541_1489-530d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(7): Show |
C | 4 | a0001c0001t0003g0101a0001c0001t0003g0106a0001c0001t0003g0108others(1): Show | 4 | HG04228.hp2 NA18968.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.1489-543_1489-530d others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(9): Show |
C | 3 | a0001c0001t0003g0110a0001c0001t0005g0081a0001c0002t0002g0175 | 3 | HG00099.hp2 HG03453.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1489-545_1489-530d others(18): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(11): Show |
C | 5 | a0001c0001t0003g0090a0001c0001t0003g0104a0001c0001t0003g0148others(2): Show | 5 | HG00408.hp1 HG00738.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1489-547_1489-530d others(20): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(13): Show |
C | 6 | a0001c0001t0003g0077a0001c0001t0003g0100a0001c0001t0005g0138others(3): Show | 6 | HG01346.hp1 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1489-549_1489-530d others(22): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(15): Show |
C | 13 | a0001c0001t0003g0097a0001c0001t0003g0134a0001c0001t0003g0152others(10): Show | 13 | HG00597.hp2 HG00639.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1489-551_1489-530d others(24): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(17): Show |
C | 26 | a0001c0001t0003g0087a0001c0001t0003g0089a0001c0001t0003g0109others(23): Show | 26 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.1489-553_1489-530d others(26): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(19): Show |
C | 29 | a0001c0001t0003g0071a0001c0001t0003g0072a0001c0001t0003g0073others(26): Show | 29 | HG00558.hp1 HG00621.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1489-555_1489-530d others(28): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(21): Show |
C | 1 | a0001c0002t0002g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1489-557_1489-530d others(30): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(25): Show |
C | 4 | a0001c0001t0004g0017a0001c0001t0004g0019a0001c0001t0004g0024others(1): Show | 4 | HG01361.hp1 HG02976.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-561_1489-530d others(34): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(27): Show |
C | 16 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022others(13): Show | 16 | HG00438.hp1 HG00738.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1489-563_1489-530d others(36): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(29): Show |
C | 21 | a0001c0001t0004g0027a0001c0001t0004g0037a0001c0001t0004g0038others(18): Show | 21 | HG01070.hp2 HG01109.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.1489-565_1489-530d others(38): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(31): Show |
C | 6 | a0001c0001t0011g0062a0001c0001t0011g0063a0001c0001t0011g0064others(3): Show | 6 | HG01074.hp1 HG02486.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1489-567_1489-530d others(40): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(37): Show |
C | 1 | a0001c0001t0007g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1489-573_1489-530d others(46): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643753
|
CTATATAT others(41): Show |
C | 67 | a0001c0001t0001g0159a0001c0001t0001g0195a0001c0001t0001g0220others(64): Show | 67 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1489-577_1489-530d others(50): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643753 | |||||
| chr20:33643757
|
A | ATATATAT others(7): Show |
1 | a0001c0002t0024g0074 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1489-577_1489-576i others(16): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643757 | |||||
| chr20:33643764
|
T | C | 2 | a0001c0001t0018g0120a0001c0001t0018g0121 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1489-583T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643764 | ||||||
| chr20:33643791
|
ATATATAT others(10): Show |
A | 1 | a0001c0002t0002g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1489-555_1489-539d others(19): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643791 | ||||||
| chr20:33643794
|
T | A | 1 | a0001c0001t0005g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1489-553T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643794 | ||||||
| chr20:33643795
|
A | G | 1 | a0001c0001t0005g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1489-552A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643795 | ||||||
| chr20:33643797
|
ATATATAT others(6): Show |
A | 4 | a0001c0001t0003g0096a0001c0001t0005g0086a0001c0001t0006g0141others(1): Show | 4 | HG01516.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-549_1489-537d others(15): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643797 | ||||||
| chr20:33643797
|
ATATATAT others(30): Show |
A | 1 | a0001c0001t0005g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1489-549_1489-513d others(39): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643797 | ||||||
| chr20:33643799
|
ATATATAT others(4): Show |
A | 1 | a0001c0002t0002g0168 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1489-547_1489-537d others(13): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643799 | ||||||
| chr20:33643799
|
ATATATAT others(32): Show |
A | 1 | a0001c0001t0003g0147 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1489-547_1489-509d others(41): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643799 | ||||||
| chr20:33643809
|
A | G | 1 | a0001c0002t0002g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1489-538A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643809 | ||||||
| chr20:33643811
|
A | AG | 3 | a0001c0001t0003g0145a0001c0002t0002g0204a0003c0009t0029g0283 | 3 | HG00735.hp1 HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1489-536_1489-535i others(3): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643811 | ||||||
| chr20:33643811
|
A | G | 11 | a0001c0001t0003g0096a0001c0001t0005g0086a0001c0001t0006g0141others(8): Show | 11 | HG01070.hp1 HG01516.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.1489-536A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643811 | ||||||
| chr20:33643813
|
A | G | 1 | a0001c0001t0005g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1489-534A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643813 | ||||||
| chr20:33643815
|
A | G | 1 | a0001c0001t0005g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1489-532A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643815 | ||||||
| chr20:33643816
|
T | A | 1 | a0001c0002t0002g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1489-531T>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643816 | ||||||
| chr20:33643817
|
A | T | 1 | a0001c0002t0002g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1489-530A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643817 | ||||||
| chr20:33643818
|
G | A | 14 | a0001c0001t0003g0096a0001c0001t0003g0145a0001c0001t0005g0086others(11): Show | 14 | HG00735.hp1 HG01070.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.1489-529G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643818 | ||||||
| chr20:33643820
|
A | G | 15 | a0001c0001t0003g0096a0001c0001t0003g0145a0001c0001t0005g0086others(12): Show | 15 | HG00735.hp1 HG01070.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1489-527A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643820 | ||||||
| chr20:33643821
|
TATA | T | 12 | a0001c0001t0003g0096a0001c0001t0003g0145a0001c0001t0005g0086others(9): Show | 12 | HG00735.hp1 HG01070.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.1489-523_1489-521d others(5): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643821 | |||||
| chr20:33643822
|
A | G | 3 | a0001c0002t0002g0187a0001c0002t0002g0191a0003c0009t0029g0283 | 3 | HG01884.hp2 HG02735.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1489-525A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643822 | ||||||
| chr20:33643824
|
A | T | 1 | a0003c0009t0029g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1489-523A>T | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643824 | ||||||
| chr20:33643825
|
A | ATG | 32 | a0001c0001t0001g0220a0001c0001t0003g0089a0001c0001t0003g0090others(29): Show | 32 | HG00323.hp2 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.1489-488_1489-487d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643825 | |||||
| chr20:33643825
|
A | ATGTG | 15 | a0001c0001t0003g0109a0001c0001t0003g0113a0001c0001t0003g0153others(12): Show | 15 | HG01496.hp2 HG02257.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1489-490_1489-487d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643825 | |||||
| chr20:33643825
|
A | G | 16 | a0001c0001t0003g0096a0001c0001t0003g0145a0001c0001t0005g0086others(13): Show | 16 | HG00735.hp1 HG01070.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.1489-522A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643825 | ||||||
| chr20:33643825
|
ATG | A | 84 | a0001c0001t0001g0159a0001c0001t0001g0222a0001c0001t0001g0223others(81): Show | 84 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1489-488_1489-487d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643825 | |||||
| chr20:33643825
|
ATGTG | A | 5 | a0001c0001t0004g0027a0001c0001t0004g0029a0001c0001t0004g0030others(2): Show | 5 | HG00438.hp1 HG01109.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1489-490_1489-487d others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643825 | |||||
| chr20:33643825
|
ATGTGTGT others(1): Show |
A | 13 | a0001c0001t0004g0017a0001c0001t0004g0020a0001c0001t0004g0021others(10): Show | 13 | HG00408.hp2 HG00544.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1489-494_1489-487d others(10): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643825 | |||||
| chr20:33643825
|
ATGTGTGT others(5): Show |
A | 4 | a0001c0001t0012g0162a0001c0001t0012g0163a0001c0001t0012g0164others(1): Show | 4 | HG01167.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1489-498_1489-487d others(14): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643825 | |||||
| chr20:33643835
|
G | A | 1 | a0001c0001t0005g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1489-512G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643835 | ||||||
| chr20:33643839
|
G | A | 1 | a0001c0001t0003g0147 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1489-508G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643839 | ||||||
| chr20:33643857
|
G | A | 1 | a0001c0001t0030g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1489-490G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643857 | ||||||
| chr20:33643859
|
G | A | 15 | a0001c0001t0004g0017a0001c0001t0004g0020a0001c0001t0004g0021others(12): Show | 15 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1489-488G>A | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643859 | ||||||
| chr20:33643859
|
G | GTA | 15 | a0001c0001t0004g0019a0001c0001t0004g0024a0001c0001t0007g0008others(12): Show | 15 | HG01261.hp2 HG01361.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1489-483_1489-482d others(4): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643859 | |||||
| chr20:33643859
|
G | GTGTA | 3 | a0001c0001t0007g0013a0001c0001t0015g0015a0001c0001t0015g0016 | 3 | HG02145.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1489-487_1489-486i others(6): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643859 | |||||
| chr20:33643859
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0015g0014 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1489-487_1489-486i others(12): Show |
CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr20 | 33643859 | |||||
| chr20:33643861
|
A | G | 14 | a0001c0001t0003g0126a0001c0001t0003g0128a0001c0001t0003g0129others(11): Show | 14 | HG00621.hp1 HG02083.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.1489-486A>G | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33643861 | ||||||
| chr20:33644190
|
T | C | 1 | a0001c0001t0004g0051 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1489-157T>C | CBFA2T2 | ENSG00000078699.22 | transcript | ENST00000342704.11 | protein_coding | 10/10 | chr20 | 33644190 |