Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4605 |
| ensemblid | ENSG00000101057.16 |
| hgncid | 7548 |
| symbol | MYBL2 |
| name | MYB proto-oncogene like 2 |
| refseq_nuc | NM_002466.4 |
| refseq_prot | NP_002457.1 |
| ensembl_nuc | ENST00000217026.5 |
| ensembl_prot | ENSP00000217026.4 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 43667114 |
| end | 43716482 |
| strand | + |
| ver | v1.2 |
| region | chr20:43667114-43716482 |
| region5000 | chr20:43662114-43721482 |
| regionname0 | MYBL2_chr20_43667114_43716482 |
| regionname5000 | MYBL2_chr20_43662114_43721482 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 700 | 188 | 50 | 43 | 71 | 2 | 20 | 53 | MYBL2_chr20_43662114_43721482 | MYBL2 | MSRRT others(695): Show |
chr20 | 43662114 | 43721482 |
| a0002 | 0/0 | 700 | 61 | 18 | 4 | 33 | 0 | 6 | 31 | MYBL2_chr20_43662114_43721482 | MYBL2 | MSRRT others(695): Show |
chr20 | 43662114 | 43721482 |
| a0003 | 0/0 | 700 | 10 | 7 | 3 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | MSRRT others(695): Show |
chr20 | 43662114 | 43721482 |
| a0004 | 0/0 | 700 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | MSRRT others(695): Show |
chr20 | 43662114 | 43721482 |
| a0005 | 0/0 | 700 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | MSRRT others(695): Show |
chr20 | 43662114 | 43721482 |
| a0006 | 0/0 | 700 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MYBL2_chr20_43662114_43721482 | MYBL2 | MSRRT others(695): Show |
chr20 | 43662114 | 43721482 |
| a0007 | 0/0 | 700 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | MSRRT others(695): Show |
chr20 | 43662114 | 43721482 |
| a0008 | 0/0 | 700 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | MSRRT others(695): Show |
chr20 | 43662114 | 43721482 |
| a0009 | 0/0 | 700 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | MSRRT others(695): Show |
chr20 | 43662114 | 43721482 |
| a0010 | 0/0 | 700 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | MSRRT others(695): Show |
chr20 | 43662114 | 43721482 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2100 | 146 | 44 | 32 | 52 | 2 | 16 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0001c0002 | 1/1 | 2100 | 38 | 4 | 11 | 17 | 0 | 4 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0001c0011 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0001c0013 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0001c0015 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0001c0017 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0002c0003 | 0/0 | 2100 | 30 | 11 | 1 | 14 | 0 | 4 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0002c0004 | 0/0 | 2100 | 25 | 2 | 2 | 19 | 0 | 2 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0002c0007 | 0/0 | 2100 | 6 | 5 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0003c0005 | 0/0 | 2100 | 10 | 7 | 3 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0004c0006 | 0/0 | 2100 | 6 | 5 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0005c0008 | 0/0 | 2100 | 3 | 3 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0006c0009 | 0/0 | 2100 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0007c0014 | 0/0 | 2100 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0008c0016 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0009c0010 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 | ||
| a0010c0012 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | ATGTC others(2095): Show |
chr20 | 43662114 | 43721482 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2668 | 143 | 41 | 32 | 52 | 2 | 16 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0001c0001t0002 | 0/0 | 2668 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0001c0001t0004 | 0/0 | 2668 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0001c0002t0001 | 1/1 | 2668 | 38 | 4 | 11 | 17 | 0 | 4 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0001c0011t0001 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0001c0013t0001 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0001c0015t0001 | 0/0 | 2668 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0001c0017t0002 | 0/0 | 2668 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0002c0003t0001 | 0/0 | 2668 | 30 | 11 | 1 | 14 | 0 | 4 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0002c0004t0001 | 0/0 | 2668 | 25 | 2 | 2 | 19 | 0 | 2 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0002c0007t0001 | 0/0 | 2668 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0002c0007t0003 | 0/0 | 2666 | 5 | 4 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2661): Show |
chr20 | 43662114 | 43721482 |
| a0003c0005t0001 | 0/0 | 2668 | 10 | 7 | 3 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0004c0006t0002 | 0/0 | 2668 | 6 | 5 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0005c0008t0001 | 0/0 | 2668 | 3 | 3 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0006c0009t0001 | 0/0 | 2668 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0007c0014t0001 | 0/0 | 2668 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0008c0016t0003 | 0/0 | 2666 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2661): Show |
chr20 | 43662114 | 43721482 |
| a0009c0010t0001 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| a0010c0012t0001 | 0/0 | 2668 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | GACTG others(2663): Show |
chr20 | 43662114 | 43721482 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0011t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0013t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0015t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0001c0017t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0004t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0007t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0007t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0007t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0007t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0007t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0002c0007t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0003c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0003c0005t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0003c0005t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0003c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0003c0005t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0003c0005t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0003c0005t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0003c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0003c0005t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0003c0005t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0004c0006t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0004c0006t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0004c0006t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0004c0006t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0004c0006t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0005c0008t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0005c0008t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0005c0008t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0006c0009t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0006c0009t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0007c0014t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0008c0016t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0009c0010t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| a0010c0012t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | CHS | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG00741 | hp2 | a0003 | c0005 | t0001 | g0120 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01081 | hp1 | a0002 | c0004 | t0001 | g0170 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01081 | hp2 | a0002 | c0003 | t0001 | g0034 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01109 | hp2 | a0002 | c0004 | t0001 | g0084 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01167 | hp1 | a0003 | c0005 | t0001 | g0117 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01243 | hp1 | a0004 | c0006 | t0002 | g0102 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01243 | hp2 | a0007 | c0014 | t0001 | g0113 | AMR | PUR | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01261 | hp2 | a0003 | c0005 | t0001 | g0122 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01361 | hp2 | a0002 | c0007 | t0003 | g0106 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01891 | hp2 | a0003 | c0005 | t0001 | g0258 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02055 | hp1 | a0004 | c0006 | t0002 | g0103 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02056 | hp1 | a0002 | c0004 | t0001 | g0074 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02083 | hp2 | a0002 | c0003 | t0001 | g0031 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | CDX | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0096 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02602 | hp2 | a0002 | c0004 | t0001 | g0012 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02615 | hp1 | a0002 | c0007 | t0003 | g0109 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02615 | hp2 | a0002 | c0004 | t0001 | g0011 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02622 | hp1 | a0001 | c0015 | t0001 | g0132 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0036 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0095 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0003 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02738 | hp2 | a0002 | c0004 | t0001 | g0013 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02818 | hp1 | a0003 | c0005 | t0001 | g0121 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02886 | hp1 | a0005 | c0008 | t0001 | g0116 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0016 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02895 | hp1 | a0003 | c0005 | t0001 | g0119 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02895 | hp2 | a0004 | c0006 | t0002 | g0104 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02896 | hp2 | a0004 | c0006 | t0002 | g0005 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02897 | hp1 | a0004 | c0006 | t0002 | g0005 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0017 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02922 | hp1 | a0002 | c0007 | t0003 | g0108 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02922 | hp2 | a0004 | c0006 | t0002 | g0101 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02965 | hp2 | a0003 | c0005 | t0001 | g0123 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03041 | hp2 | a0002 | c0004 | t0001 | g0076 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0040 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03225 | hp1 | a0008 | c0016 | t0003 | g0252 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03453 | hp2 | a0005 | c0008 | t0001 | g0114 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03486 | hp1 | a0001 | c0017 | t0002 | g0124 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0021 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03492 | hp2 | a0002 | c0003 | t0001 | g0022 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ESN | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03540 | hp2 | a0002 | c0007 | t0003 | g0110 | AFR | GWD | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0037 | AFR | MSL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0235 | SAS | STU | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0090 | SAS | PJL | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG04228 | hp1 | a0002 | c0003 | t0001 | g0038 | SAS | STU | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18612 | hp2 | a0001 | c0013 | t0001 | g0053 | EAS | CHB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18939 | hp2 | a0002 | c0004 | t0001 | g0087 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18946 | hp2 | a0002 | c0004 | t0001 | g0041 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18950 | hp1 | a0002 | c0004 | t0001 | g0077 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18952 | hp2 | a0002 | c0003 | t0001 | g0030 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18959 | hp1 | a0009 | c0010 | t0001 | g0054 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18963 | hp2 | a0002 | c0004 | t0001 | g0045 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18966 | hp1 | a0006 | c0009 | t0001 | g0148 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18966 | hp2 | a0002 | c0004 | t0001 | g0078 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18967 | hp2 | a0002 | c0003 | t0001 | g0217 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18968 | hp1 | a0002 | c0004 | t0001 | g0079 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0024 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18972 | hp2 | a0002 | c0003 | t0001 | g0032 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18975 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18982 | hp2 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18983 | hp2 | a0002 | c0004 | t0001 | g0097 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18984 | hp2 | a0002 | c0004 | t0001 | g0047 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18990 | hp1 | a0002 | c0004 | t0001 | g0042 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18992 | hp1 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18993 | hp1 | a0002 | c0004 | t0001 | g0085 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18994 | hp2 | a0002 | c0003 | t0001 | g0027 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18995 | hp2 | a0002 | c0004 | t0001 | g0080 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19000 | hp2 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19003 | hp2 | a0006 | c0009 | t0001 | g0231 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19009 | hp2 | a0002 | c0004 | t0001 | g0048 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19011 | hp1 | a0002 | c0004 | t0001 | g0082 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19030 | hp2 | a0003 | c0005 | t0001 | g0259 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0028 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19058 | hp1 | a0010 | c0012 | t0001 | g0243 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19058 | hp2 | a0002 | c0003 | t0001 | g0029 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19063 | hp2 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19068 | hp1 | a0001 | c0011 | t0001 | g0257 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19070 | hp1 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19077 | hp1 | a0002 | c0004 | t0001 | g0098 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19077 | hp2 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19085 | hp2 | a0002 | c0004 | t0001 | g0083 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19088 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19089 | hp2 | a0002 | c0004 | t0001 | g0075 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0003 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA19240 | hp2 | a0002 | c0007 | t0003 | g0107 | AFR | YRI | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ASW | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ASW | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0026 | SAS | GIH | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | GIH | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02109 | hp1 | a0003 | c0005 | t0001 | g0115 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02486 | hp1 | a0005 | c0008 | t0001 | g0112 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0035 | AFR | ACB | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG06807 | hp1 | a0003 | c0005 | t0001 | g0118 | AFR | USA | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | USA | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA18955 | hp2 | a0002 | c0004 | t0001 | g0081 | EAS | JPT | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | USA | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA20300 | hp2 | a0002 | c0007 | t0001 | g0111 | AFR | USA | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0059 | REF | REF | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0056 | REF | REF | MYBL2_chr20_43662114_43721482 | MYBL2 | chr20 | 43662114 | 43721482 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:43681809 | G | A | 1 | a0008 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.140G>A | p.Arg47Lys | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/14 | 310/2668 | 140/2103 | 47/700 | chr20 | 43681809 | |||
| chr20:43681838 | C | A | 1 | a0009 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.169C>A | p.Leu57Met | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/14 | 339/2668 | 169/2103 | 57/700 | chr20 | 43681838 | |||
| chr20:43692228 | G | A | 1 | a0004 | 6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
missense_variant | MODERATE | c.572G>A | p.Ser191Asn | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/14 | 742/2668 | 572/2103 | 191/700 | chr20 | 43692228 | |||
| chr20:43699914 | C | T | 1 | a0007 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.821C>T | p.Pro274Leu | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/14 | 991/2668 | 821/2103 | 274/700 | chr20 | 43699914 | |||
| chr20:43702560 | A | G | 1 | a0005 | 3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.1022A>G | p.Asn341Ser | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/14 | 1192/2668 | 1022/2103 | 341/700 | chr20 | 43702560 | |||
| chr20:43702817 | A | G | 4 | a0002 a0003 a0005 others(1): Show |
75 | HG00741.hp2 HG01081.hp1 HG01081.hp2 others(72): Show |
missense_variant | MODERATE | c.1279A>G | p.Ser427Gly | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/14 | 1449/2668 | 1279/2103 | 427/700 | chr20 | 43702817 | |||
| chr20:43705358 | C | T | 1 | a0010 | 1 | NA19058.hp1 | missense_variant&splice_region_variant | MODERATE | c.1505C>T | p.Ala502Val | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/14 | 1675/2668 | 1505/2103 | 502/700 | chr20 | 43705358 | |||
| chr20:43713065 | G | A | 2 | a0003 a0007 |
11 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(8): Show |
missense_variant | MODERATE | c.1783G>A | p.Val595Met | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/14 | 1953/2668 | 1783/2103 | 595/700 | chr20 | 43713065 | |||
| chr20:43715137 | A | G | 1 | a0006 | 2 | NA18966.hp1 NA19003.hp2 |
missense_variant | MODERATE | c.1828A>G | p.Thr610Ala | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/14 | 1998/2668 | 1828/2103 | 610/700 | chr20 | 43715137 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:43681786 | C | T | 4 | a0001c0017 a0002c0007 a0004c0006 others(1): Show |
14 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.117C>T | p.Asp39Asp | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/14 | 287/2668 | 117/2103 | 39/700 | chr20 | 43681786 | |||
| chr20:43687052 | C | T | 1 | a0001c0015 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.480C>T | p.Ile160Ile | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/14 | 650/2668 | 480/2103 | 160/700 | chr20 | 43687052 | |||
| chr20:43692241 | C | T | 1 | a0002c0004 | 25 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(22): Show |
synonymous_variant | LOW | c.585C>T | p.Asp195Asp | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/14 | 755/2668 | 585/2103 | 195/700 | chr20 | 43692241 | |||
| chr20:43699999 | T | C | 14 | a0001c0001 a0001c0011 a0001c0015 others(11): Show |
234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
synonymous_variant | LOW | c.906T>C | p.Pro302Pro | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/14 | 1076/2668 | 906/2103 | 302/700 | chr20 | 43699999 | |||
| chr20:43702756 | G | A | 1 | a0001c0011 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.1218G>A | p.Pro406Pro | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/14 | 1388/2668 | 1218/2103 | 406/700 | chr20 | 43702756 | |||
| chr20:43711565 | C | T | 1 | a0001c0013 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.1683C>T | p.Asp561Asp | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/14 | 1853/2668 | 1683/2103 | 561/700 | chr20 | 43711565 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:43667258 | A | G | 1 | a0001c0001t0004 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-26A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/14 | 26 | chr20 | 43667258 | ||||||
| chr20:43716105 | G | A | 3 | a0001c0001t0002 a0001c0017t0002 a0004c0006t0002 |
9 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*18G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 14/14 | 18 | chr20 | 43716105 | ||||||
| chr20:43716215 | ACT | A | 2 | a0002c0007t0003 a0008c0016t0003 |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*132_*133delTC | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 14/14 | 132 | INFO_REALIGN_3_PRIME | chr20 | 43716215 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:43667385 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.20+82C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667385 | |||||||
| chr20:43667663 | A | G | 4 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0260 others(1): Show |
6 | HG01255.hp2 HG01496.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+360A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667663 | |||||||
| chr20:43667788 | G | T | 1 | a0003c0005t0001g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.20+485G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667788 | |||||||
| chr20:43667797 | A | G | 1 | a0003c0005t0001g0258 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.20+494A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667797 | |||||||
| chr20:43667880 | C | G | 1 | a0001c0011t0001g0257 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.20+577C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667880 | |||||||
| chr20:43667902 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(157): Show |
167 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.20+599C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667902 | |||||||
| chr20:43667911 | T | C | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.20+608T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667911 | |||||||
| chr20:43667924 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.20+621A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667924 | |||||||
| chr20:43667933 | C | T | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+630C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667933 | |||||||
| chr20:43667952 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.20+649G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667952 | |||||||
| chr20:43667998 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.20+695C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43667998 | |||||||
| chr20:43668004 | A | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): Show |
147 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.20+701A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668004 | |||||||
| chr20:43668042 | C | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.20+739C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668042 | |||||||
| chr20:43668075 | T | G | 4 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+772T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668075 | |||||||
| chr20:43668096 | T | A | 24 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(21): Show |
25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.20+793T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668096 | |||||||
| chr20:43668194 | C | CT | 15 | a0001c0001t0001g0088 a0001c0002t0001g0089 a0001c0002t0001g0090 others(12): Show |
15 | HG01175.hp1 HG01192.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.20+915dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | ||||||
| chr20:43668194 | CT | C | 14 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0049 others(11): Show |
14 | HG02615.hp2 HG02717.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.20+915delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | ||||||
| chr20:43668194 | CTT | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0225 a0001c0001t0001g0226 others(30): Show |
34 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.20+914_20+915delTT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | ||||||
| chr20:43668194 | CTTT | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): Show |
138 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.20+913_20+915delTT others(1): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | ||||||
| chr20:43668194 | CTTTT | C | 18 | a0001c0001t0001g0125 a0003c0005t0001g0115 a0003c0005t0001g0117 others(15): Show |
19 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.20+912_20+915delTT others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | ||||||
| chr20:43668194 | CTTTTTTT others(4): Show |
C | 6 | a0002c0007t0001g0111 a0002c0007t0003g0106 a0002c0007t0003g0107 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.20+905_20+915delTT others(9): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668194 | ||||||
| chr20:43668261 | C | T | 24 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(21): Show |
25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.20+958C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668261 | |||||||
| chr20:43668321 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(200): Show |
212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.20+1018T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668321 | |||||||
| chr20:43668324 | C | G | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+1021C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668324 | |||||||
| chr20:43668340 | T | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(150): Show |
160 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.20+1037T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668340 | |||||||
| chr20:43668346 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(243): Show |
258 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(255): Show |
intron_variant | MODIFIER | c.20+1043A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668346 | |||||||
| chr20:43668514 | C | T | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+1211C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668514 | |||||||
| chr20:43668660 | C | T | 1 | a0002c0003t0001g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.20+1357C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668660 | |||||||
| chr20:43668664 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG03239.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.20+1361C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668664 | |||||||
| chr20:43668685 | G | GT | 22 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0088 others(19): Show |
24 | HG01255.hp2 HG01261.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.20+1402dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668685 | ||||||
| chr20:43668685 | G | GTT | 23 | a0001c0001t0001g0044 a0001c0002t0001g0261 a0002c0003t0001g0003 others(20): Show |
24 | HG01081.hp2 HG01934.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.20+1401_20+1402dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668685 | ||||||
| chr20:43668685 | GT | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
142 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(139): Show |
intron_variant | MODIFIER | c.20+1402delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43668685 | ||||||
| chr20:43668726 | A | C | 40 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0002g0050 others(37): Show |
41 | HG01081.hp2 HG01361.hp2 HG02083.hp2 others(38): Show |
intron_variant | MODIFIER | c.20+1423A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668726 | |||||||
| chr20:43668726 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0088 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.20+1423A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668726 | |||||||
| chr20:43668771 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(200): Show |
212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.20+1468C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668771 | |||||||
| chr20:43668930 | A | G | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+1627A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43668930 | |||||||
| chr20:43669015 | C | T | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+1712C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669015 | |||||||
| chr20:43669021 | G | A | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+1718G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669021 | |||||||
| chr20:43669082 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0244 |
2 | HG03239.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.20+1779G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669082 | |||||||
| chr20:43669138 | G | A | 1 | a0004c0006t0002g0101 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.20+1835G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669138 | |||||||
| chr20:43669202 | A | G | 2 | a0001c0001t0001g0207 a0010c0012t0001g0243 |
2 | NA18992.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.20+1899A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669202 | |||||||
| chr20:43669347 | G | C | 1 | a0001c0001t0001g0125 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.20+2044G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669347 | |||||||
| chr20:43669413 | G | C | 3 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0003c0005t0001g0259 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.20+2110G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669413 | |||||||
| chr20:43669513 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.20+2210C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669513 | |||||||
| chr20:43669806 | A | T | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+2503A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669806 | |||||||
| chr20:43669975 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18967.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.20+2672G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669975 | |||||||
| chr20:43669977 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0088 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.20+2674G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43669977 | |||||||
| chr20:43670023 | T | G | 6 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0045 others(3): Show |
6 | NA18946.hp2 NA18963.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+2720T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670023 | |||||||
| chr20:43670109 | T | TAAAC | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.20+2824_20+2827dup others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670109 | ||||||
| chr20:43670352 | T | A | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+3049T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670352 | |||||||
| chr20:43670469 | A | C | 25 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(22): Show |
26 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.20+3166A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670469 | |||||||
| chr20:43670639 | A | G | 7 | a0003c0005t0001g0117 a0003c0005t0001g0118 a0003c0005t0001g0119 others(4): Show |
7 | HG00741.hp2 HG01167.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-3167A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670639 | |||||||
| chr20:43670888 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.21-2918C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670888 | |||||||
| chr20:43670953 | A | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.21-2853A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670953 | |||||||
| chr20:43670960 | C | CT | 21 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0002c0003t0001g0019 others(18): Show |
21 | HG02083.hp2 HG02615.hp1 HG02723.hp2 others(18): Show |
intron_variant | MODIFIER | c.21-2838dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670960 | ||||||
| chr20:43670960 | C | CTT | 9 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0033 others(6): Show |
10 | HG01081.hp2 HG02486.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-2839_21-2838dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670960 | ||||||
| chr20:43670960 | CTTTTTTT others(8): Show |
C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(150): Show |
160 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.21-2837_21-2823del others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670960 | ||||||
| chr20:43670960 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0129 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.21-2837_21-2822del others(16): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670960 | ||||||
| chr20:43670967 | TTC | T | 8 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 others(5): Show |
9 | HG01243.hp1 HG02055.hp1 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.21-2837_21-2836del others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43670967 | ||||||
| chr20:43670968 | TC | T | 4 | a0002c0004t0001g0041 a0002c0004t0001g0047 a0002c0004t0001g0076 others(1): Show |
4 | HG03041.hp2 NA18939.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.21-2837delC | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670968 | |||||||
| chr20:43670969 | C | T | 50 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0017t0002g0124 others(47): Show |
51 | HG01081.hp2 HG01109.hp2 HG01361.hp2 others(48): Show |
intron_variant | MODIFIER | c.21-2837C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43670969 | |||||||
| chr20:43671093 | C | T | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-2713C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671093 | |||||||
| chr20:43671188 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(151): Show |
161 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.21-2618G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671188 | |||||||
| chr20:43671274 | T | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(156): Show |
167 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.21-2532T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671274 | |||||||
| chr20:43671451 | C | T | 1 | a0002c0007t0003g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.21-2355C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671451 | |||||||
| chr20:43671463 | A | AT | 41 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0192 others(38): Show |
41 | HG01167.hp2 HG01175.hp1 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.21-2319dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | ||||||
| chr20:43671463 | A | ATT | 29 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0220 others(26): Show |
29 | HG00741.hp2 HG01261.hp1 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.21-2320_21-2319dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | ||||||
| chr20:43671463 | A | ATTT | 22 | a0001c0001t0001g0043 a0002c0003t0001g0003 a0002c0003t0001g0019 others(19): Show |
23 | HG01081.hp2 HG01109.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.21-2321_21-2319dup others(3): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | ||||||
| chr20:43671463 | A | ATTTT | 8 | a0001c0001t0001g0044 a0001c0001t0001g0088 a0002c0003t0001g0018 others(5): Show |
8 | HG01884.hp1 HG02083.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.21-2322_21-2319dup others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | ||||||
| chr20:43671463 | A | ATTTTT | 6 | a0001c0001t0001g0052 a0002c0003t0001g0014 a0002c0003t0001g0015 others(3): Show |
6 | HG02630.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-2323_21-2319dup others(5): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | ||||||
| chr20:43671463 | ATTTTTTT | A | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-2325_21-2319del others(7): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | ||||||
| chr20:43671463 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0208 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.21-2331_21-2319del others(13): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43671463 | ||||||
| chr20:43671484 | T | G | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-2322T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671484 | |||||||
| chr20:43671486 | T | G | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-2320T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671486 | |||||||
| chr20:43671506 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.21-2300C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671506 | |||||||
| chr20:43671622 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(201): Show |
213 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(210): Show |
intron_variant | MODIFIER | c.21-2184A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671622 | |||||||
| chr20:43671644 | G | A | 1 | a0002c0004t0001g0074 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.21-2162G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671644 | |||||||
| chr20:43671770 | C | T | 4 | a0001c0001t0001g0105 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | NA18941.hp2 NA18951.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.21-2036C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671770 | |||||||
| chr20:43671841 | T | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(222): Show |
234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.21-1965T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671841 | |||||||
| chr20:43671935 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.21-1871C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671935 | |||||||
| chr20:43671947 | C | G | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-1859C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671947 | |||||||
| chr20:43671964 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.21-1842C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43671964 | |||||||
| chr20:43672085 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(156): Show |
167 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.21-1721T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672085 | |||||||
| chr20:43672138 | G | A | 1 | a0001c0013t0001g0053 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.21-1668G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672138 | |||||||
| chr20:43672229 | C | CTGTACAC others(40): Show |
161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(158): Show |
169 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.21-1531_21-1530ins others(47): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43672229 | ||||||
| chr20:43672229 | C | CTGTACTC others(40): Show |
1 | a0001c0001t0001g0247 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.21-1572_21-1571ins others(47): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43672229 | ||||||
| chr20:43672427 | CA | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(179): Show |
191 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.21-1365delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43672427 | ||||||
| chr20:43672454 | A | G | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.21-1352A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672454 | |||||||
| chr20:43672843 | C | T | 1 | a0005c0008t0001g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.21-963C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672843 | |||||||
| chr20:43672855 | T | G | 1 | a0001c0001t0001g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.21-951T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672855 | |||||||
| chr20:43672897 | C | T | 6 | a0002c0007t0001g0111 a0002c0007t0003g0106 a0002c0007t0003g0107 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-909C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672897 | |||||||
| chr20:43672900 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.21-906T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672900 | |||||||
| chr20:43672915 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0240 |
3 | HG02055.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.21-891C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43672915 | |||||||
| chr20:43673246 | C | CT | 20 | a0002c0004t0001g0042 a0002c0004t0001g0045 a0002c0004t0001g0046 others(17): Show |
20 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(17): Show |
intron_variant | MODIFIER | c.21-544dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43673246 | ||||||
| chr20:43673246 | CT | C | 45 | a0001c0001t0001g0063 a0001c0001t0001g0185 a0001c0001t0001g0186 others(42): Show |
46 | HG00738.hp2 HG01081.hp2 HG01361.hp2 others(43): Show |
intron_variant | MODIFIER | c.21-544delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43673246 | ||||||
| chr20:43673246 | CTT | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): Show |
158 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.21-545_21-544delTT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr20 | 43673246 | ||||||
| chr20:43673511 | C | T | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-295C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673511 | |||||||
| chr20:43673561 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(110): Show |
119 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.21-245C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673561 | |||||||
| chr20:43673679 | A | C | 3 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0003c0005t0001g0259 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.21-127A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673679 | |||||||
| chr20:43673695 | C | T | 1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.21-111C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673695 | |||||||
| chr20:43673731 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(149): Show |
159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.21-75C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673731 | |||||||
| chr20:43673741 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18967.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.21-65A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673741 | |||||||
| chr20:43673742 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.21-64C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 1/13 | chr20 | 43673742 | |||||||
| chr20:43674018 | G | T | 1 | a0003c0005t0001g0119 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.114+119G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674018 | |||||||
| chr20:43674101 | G | C | 24 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(21): Show |
25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.114+202G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674101 | |||||||
| chr20:43674103 | G | A | 3 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0003c0005t0001g0259 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.114+204G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674103 | |||||||
| chr20:43674127 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0183 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.114+228C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674127 | |||||||
| chr20:43674224 | T | TC | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(36): Show |
43 | HG00280.hp1 HG00544.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.114+331dupC | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43674224 | ||||||
| chr20:43674224 | T | TCC | 41 | a0001c0001t0001g0006 a0001c0001t0001g0127 a0001c0001t0001g0128 others(38): Show |
42 | HG00642.hp1 HG00642.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.114+330_114+331dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43674224 | ||||||
| chr20:43674224 | T | TCCC | 14 | a0001c0001t0001g0130 a0001c0001t0001g0177 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp1 HG01099.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+329_114+331dup others(3): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43674224 | ||||||
| chr20:43674230 | CA | C | 7 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0119 others(4): Show |
7 | HG00741.hp2 HG01167.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+332delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674230 | |||||||
| chr20:43674231 | A | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(148): Show |
159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.114+332A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674231 | |||||||
| chr20:43674234 | C | CCCCT | 13 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(10): Show |
13 | HG00673.hp1 HG00673.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+335_114+336ins others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674234 | |||||||
| chr20:43674234 | C | CCCT | 27 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0125 others(24): Show |
29 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.114+335_114+336ins others(3): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674234 | |||||||
| chr20:43674234 | C | CCT | 4 | a0001c0001t0001g0229 a0004c0006t0002g0005 a0004c0006t0002g0101 others(1): Show |
5 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+335_114+336ins others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674234 | |||||||
| chr20:43674234 | C | CT | 25 | a0001c0001t0001g0052 a0001c0001t0001g0088 a0001c0002t0001g0004 others(22): Show |
28 | HG00544.hp2 HG01255.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.114+354dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43674234 | ||||||
| chr20:43674235 | T | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0154 a0001c0001t0001g0155 others(9): Show |
13 | HG00741.hp2 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+336T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674235 | |||||||
| chr20:43674370 | G | A | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+471G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674370 | |||||||
| chr20:43674391 | AT | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(159): Show |
170 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.114+507delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43674391 | ||||||
| chr20:43674417 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.114+518C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674417 | |||||||
| chr20:43674467 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0208 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.114+568A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674467 | |||||||
| chr20:43674559 | T | C | 1 | a0002c0003t0001g0036 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.114+660T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674559 | |||||||
| chr20:43674569 | A | G | 1 | a0003c0005t0001g0122 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.114+670A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674569 | |||||||
| chr20:43674616 | G | A | 24 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(21): Show |
25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.114+717G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674616 | |||||||
| chr20:43674663 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.114+764G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674663 | |||||||
| chr20:43674675 | T | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG02258.hp2 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.114+776T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674675 | |||||||
| chr20:43674685 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.114+786C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674685 | |||||||
| chr20:43674907 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18967.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.114+1008T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674907 | |||||||
| chr20:43674924 | T | G | 1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.114+1025T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674924 | |||||||
| chr20:43674988 | T | A | 19 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(16): Show |
19 | HG00738.hp2 HG00741.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.114+1089T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43674988 | |||||||
| chr20:43675138 | C | A | 1 | a0005c0008t0001g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.114+1239C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675138 | |||||||
| chr20:43675316 | T | C | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+1417T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675316 | |||||||
| chr20:43675322 | C | CT | 5 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 others(2): Show |
5 | HG02602.hp2 HG02615.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+1436dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675322 | ||||||
| chr20:43675322 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.114+1423C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675322 | |||||||
| chr20:43675323 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.114+1424T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675323 | |||||||
| chr20:43675336 | G | T | 10 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+1437G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675336 | |||||||
| chr20:43675338 | G | A | 10 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+1439G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675338 | |||||||
| chr20:43675340 | T | C | 1 | a0001c0002t0001g0261 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.114+1441T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675340 | |||||||
| chr20:43675761 | T | TTG | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(141): Show |
150 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.114+1886_114+1887d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675761 | ||||||
| chr20:43675761 | T | TTGTG | 31 | a0001c0001t0001g0008 a0001c0001t0001g0161 a0001c0001t0001g0186 others(28): Show |
33 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.114+1884_114+1887d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675761 | ||||||
| chr20:43675761 | T | TTGTGTG | 12 | a0001c0001t0001g0185 a0001c0017t0002g0124 a0002c0003t0001g0014 others(9): Show |
12 | HG01361.hp2 HG02258.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114+1882_114+1887d others(8): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675761 | ||||||
| chr20:43675761 | T | TTGTGTGT others(1): Show |
3 | a0002c0007t0003g0108 a0003c0005t0001g0123 a0008c0016t0003g0252 |
3 | HG02922.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.114+1880_114+1887d others(10): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675761 | ||||||
| chr20:43675761 | T | TTGTGTGT others(3): Show |
9 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(6): Show |
9 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+1878_114+1887d others(12): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675761 | ||||||
| chr20:43675894 | G | A | 1 | a0001c0002t0001g0235 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.114+1995G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675894 | |||||||
| chr20:43675911 | G | GTT | 15 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(12): Show |
16 | HG00741.hp2 HG01167.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.114+2024_114+2025d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675911 | ||||||
| chr20:43675911 | G | GTTT | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(136): Show |
146 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.114+2023_114+2025d others(5): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43675911 | ||||||
| chr20:43675935 | C | T | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.114+2036C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675935 | |||||||
| chr20:43675952 | T | C | 1 | a0003c0005t0001g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.114+2053T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43675952 | |||||||
| chr20:43676047 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.114+2148G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676047 | |||||||
| chr20:43676104 | C | T | 1 | a0002c0003t0001g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114+2205C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676104 | |||||||
| chr20:43676351 | A | G | 1 | a0002c0004t0001g0083 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.114+2452A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676351 | |||||||
| chr20:43676601 | T | C | 1 | a0002c0007t0003g0107 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114+2702T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676601 | |||||||
| chr20:43676613 | C | T | 7 | a0002c0003t0001g0003 a0002c0003t0001g0028 a0002c0003t0001g0034 others(4): Show |
8 | HG01081.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2714C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676613 | |||||||
| chr20:43676616 | T | A | 3 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0003c0005t0001g0259 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.114+2717T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676616 | |||||||
| chr20:43676874 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0208 |
2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.114+2975T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43676874 | |||||||
| chr20:43676878 | G | GT | 7 | a0001c0001t0001g0001 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
9 | HG00673.hp2 HG01255.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.114+2990dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43676878 | ||||||
| chr20:43676878 | GT | G | 9 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0003c0005t0001g0259 others(6): Show |
10 | HG01243.hp1 HG02055.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+2990delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43676878 | ||||||
| chr20:43677039 | T | C | 21 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0045 others(18): Show |
21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.114+3140T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677039 | |||||||
| chr20:43677274 | G | C | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.114+3375G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677274 | |||||||
| chr20:43677289 | G | C | 1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.114+3390G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677289 | |||||||
| chr20:43677416 | A | G | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+3517A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677416 | |||||||
| chr20:43677427 | G | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0256 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.114+3528G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677427 | |||||||
| chr20:43677449 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.114+3550A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677449 | |||||||
| chr20:43677547 | A | G | 3 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0003c0005t0001g0259 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.114+3648A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677547 | |||||||
| chr20:43677579 | C | T | 1 | a0002c0007t0003g0106 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.114+3680C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677579 | |||||||
| chr20:43677615 | C | T | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+3716C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677615 | |||||||
| chr20:43677620 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(155): Show |
166 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.114+3721A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677620 | |||||||
| chr20:43677652 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(200): Show |
212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.114+3753T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677652 | |||||||
| chr20:43677667 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(155): Show |
166 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.114+3768A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677667 | |||||||
| chr20:43677669 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(200): Show |
212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.114+3770T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677669 | |||||||
| chr20:43677769 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.114+3870C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677769 | |||||||
| chr20:43677839 | A | C | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.114+3940A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677839 | |||||||
| chr20:43677896 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-3888G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43677896 | |||||||
| chr20:43678067 | TGCAAGAT others(26): Show |
T | 1 | a0001c0001t0001g0225 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.115-3713_115-3681d others(35): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678067 | ||||||
| chr20:43678092 | C | T | 1 | a0003c0005t0001g0119 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.115-3692C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678092 | |||||||
| chr20:43678173 | C | T | 1 | a0002c0007t0003g0110 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.115-3611C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678173 | |||||||
| chr20:43678212 | T | C | 10 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-3572T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678212 | |||||||
| chr20:43678275 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.115-3509C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678275 | |||||||
| chr20:43678303 | AAAAT | A | 48 | a0001c0001t0001g0008 a0001c0001t0001g0176 a0001c0001t0001g0185 others(45): Show |
50 | HG00738.hp2 HG00741.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.115-3473_115-3470d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678303 | ||||||
| chr20:43678311 | T | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(110): Show |
119 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.115-3473T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678311 | |||||||
| chr20:43678311 | TAAAG | T | 11 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(8): Show |
11 | HG01884.hp1 HG02602.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-3453_115-3450d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678311 | ||||||
| chr20:43678319 | GAAAGAAA others(10): Show |
G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0206 |
2 | HG01071.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.115-3461_115-3445d others(19): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678319 | ||||||
| chr20:43678323 | GAAAGAAA others(6): Show |
G | 7 | a0001c0001t0001g0140 a0001c0001t0001g0161 a0001c0001t0001g0173 others(4): Show |
7 | HG00642.hp1 HG00642.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-3457_115-3445d others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678323 | ||||||
| chr20:43678327 | GAAAGAAA others(2): Show |
G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(106): Show |
115 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.115-3453_115-3445d others(11): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678327 | ||||||
| chr20:43678327 | GAAAGAAA others(3): Show |
G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0230 |
2 | HG01346.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.115-3453_115-3444d others(12): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678327 | ||||||
| chr20:43678331 | GAAAAA | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0142 a0001c0001t0001g0176 others(29): Show |
33 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.115-3442_115-3438d others(7): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678331 | ||||||
| chr20:43678332 | A | AAAG | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-3450_115-3449i others(5): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678332 | ||||||
| chr20:43678349 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.115-3435A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678349 | |||||||
| chr20:43678452 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(155): Show |
166 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.115-3332A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678452 | |||||||
| chr20:43678466 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115-3318C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678466 | |||||||
| chr20:43678505 | A | G | 1 | a0003c0005t0001g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.115-3279A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678505 | |||||||
| chr20:43678791 | A | G | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-2993A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678791 | |||||||
| chr20:43678835 | C | A | 1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115-2949C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678835 | |||||||
| chr20:43678857 | C | CA | 5 | a0001c0001t0001g0219 a0004c0006t0002g0005 a0004c0006t0002g0101 others(2): Show |
6 | HG01243.hp1 HG01255.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-2910dupA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678857 | ||||||
| chr20:43678871 | AAAAG | A | 37 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0002g0050 others(34): Show |
38 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(35): Show |
intron_variant | MODIFIER | c.115-2909_115-2906d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678871 | ||||||
| chr20:43678873 | AAG | A | 6 | a0001c0001t0001g0125 a0001c0001t0001g0161 a0001c0001t0001g0166 others(3): Show |
6 | HG01081.hp1 HG01167.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-2909_115-2908d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678873 | ||||||
| chr20:43678874 | AG | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(120): Show |
129 | HG00280.hp1 HG00544.hp1 HG00673.hp1 others(126): Show |
intron_variant | MODIFIER | c.115-2909delG | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678874 | |||||||
| chr20:43678875 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0133 a0001c0001t0001g0137 others(26): Show |
30 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.115-2909G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678875 | |||||||
| chr20:43678883 | CAT | C | 10 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-2897_115-2896d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43678883 | ||||||
| chr20:43678929 | G | A | 6 | a0002c0007t0001g0111 a0002c0007t0003g0106 a0002c0007t0003g0107 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-2855G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678929 | |||||||
| chr20:43678951 | A | C | 10 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0017t0002g0124 others(7): Show |
10 | HG01361.hp2 HG02615.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-2833A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43678951 | |||||||
| chr20:43679000 | T | C | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(3): Show |
6 | HG00673.hp1 HG01109.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-2784T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679000 | |||||||
| chr20:43679072 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(221): Show |
233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.115-2712A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679072 | |||||||
| chr20:43679194 | T | C | 7 | a0003c0005t0001g0117 a0003c0005t0001g0118 a0003c0005t0001g0119 others(4): Show |
7 | HG00741.hp2 HG01167.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-2590T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679194 | |||||||
| chr20:43679195 | A | T | 1 | a0001c0001t0001g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.115-2589A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679195 | |||||||
| chr20:43679268 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0195 |
2 | NA18959.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.115-2516C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679268 | |||||||
| chr20:43679325 | G | A | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-2459G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679325 | |||||||
| chr20:43679473 | GA | G | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.115-2308delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43679473 | ||||||
| chr20:43679517 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.115-2267C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679517 | |||||||
| chr20:43679535 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.115-2249G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679535 | |||||||
| chr20:43679577 | T | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(201): Show |
213 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(210): Show |
intron_variant | MODIFIER | c.115-2207T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679577 | |||||||
| chr20:43679707 | C | G | 1 | a0002c0003t0001g0035 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.115-2077C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679707 | |||||||
| chr20:43679727 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0143 |
2 | HG01109.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.115-2057T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679727 | |||||||
| chr20:43679851 | CGG | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(199): Show |
211 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.115-1930_115-1929d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43679851 | ||||||
| chr20:43679853 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.115-1931G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679853 | |||||||
| chr20:43679912 | CA | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(148): Show |
158 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.115-1859delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43679912 | ||||||
| chr20:43679928 | A | T | 1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115-1856A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43679928 | |||||||
| chr20:43680024 | TTTTA | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(149): Show |
159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.115-1748_115-1745d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr20 | 43680024 | ||||||
| chr20:43680075 | T | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(201): Show |
213 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(210): Show |
intron_variant | MODIFIER | c.115-1709T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680075 | |||||||
| chr20:43680089 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.115-1695G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680089 | |||||||
| chr20:43680176 | G | A | 6 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(3): Show |
7 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-1608G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680176 | |||||||
| chr20:43680182 | C | G | 3 | a0005c0008t0001g0112 a0005c0008t0001g0114 a0005c0008t0001g0116 |
3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.115-1602C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680182 | |||||||
| chr20:43680308 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(165): Show |
176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.115-1476A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680308 | |||||||
| chr20:43680373 | A | G | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.115-1411A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680373 | |||||||
| chr20:43680514 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(221): Show |
233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.115-1270T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680514 | |||||||
| chr20:43680644 | A | G | 1 | a0010c0012t0001g0243 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.115-1140A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680644 | |||||||
| chr20:43680739 | C | T | 1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115-1045C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680739 | |||||||
| chr20:43680740 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(200): Show |
212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.115-1044A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680740 | |||||||
| chr20:43680906 | C | T | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-878C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680906 | |||||||
| chr20:43680945 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(148): Show |
158 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.115-839C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680945 | |||||||
| chr20:43680981 | A | G | 10 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-803A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43680981 | |||||||
| chr20:43681168 | T | C | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-616T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681168 | |||||||
| chr20:43681276 | C | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(149): Show |
159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.115-508C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681276 | |||||||
| chr20:43681292 | C | G | 1 | a0004c0006t0002g0102 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.115-492C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681292 | |||||||
| chr20:43681359 | C | G | 10 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-425C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681359 | |||||||
| chr20:43681374 | A | G | 24 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(21): Show |
25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.115-410A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681374 | |||||||
| chr20:43681378 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(149): Show |
159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.115-406A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681378 | |||||||
| chr20:43681608 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.115-176G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681608 | |||||||
| chr20:43681657 | T | C | 21 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0045 others(18): Show |
21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.115-127T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 2/13 | chr20 | 43681657 | |||||||
| chr20:43681869 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(165): Show |
176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.186+14T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43681869 | |||||||
| chr20:43681886 | G | A | 10 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.186+31G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43681886 | |||||||
| chr20:43682036 | G | T | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.186+181G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682036 | |||||||
| chr20:43682171 | A | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(148): Show |
158 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.186+316A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682171 | |||||||
| chr20:43682244 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0146 a0001c0001t0001g0193 others(1): Show |
4 | HG00280.hp2 HG01175.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+389G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682244 | |||||||
| chr20:43682249 | C | CACATTCG others(298): Show |
3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.186+408_186+409ins others(305): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43682249 | ||||||
| chr20:43682263 | T | TA | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(5): Show |
8 | HG01884.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+409dupA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr20 | 43682263 | ||||||
| chr20:43682430 | C | T | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.187-364C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682430 | |||||||
| chr20:43682448 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(165): Show |
176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.187-346T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682448 | |||||||
| chr20:43682479 | T | C | 10 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-315T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682479 | |||||||
| chr20:43682511 | G | A | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.187-283G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682511 | |||||||
| chr20:43682582 | A | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(221): Show |
233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.187-212A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 3/13 | chr20 | 43682582 | |||||||
| chr20:43682947 | C | T | 1 | a0001c0002t0001g0073 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.279+61C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43682947 | |||||||
| chr20:43683215 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(165): Show |
176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.279+329T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683215 | |||||||
| chr20:43683383 | C | G | 6 | a0002c0007t0001g0111 a0002c0007t0003g0106 a0002c0007t0003g0107 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+497C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683383 | |||||||
| chr20:43683389 | G | T | 6 | a0002c0007t0001g0111 a0002c0007t0003g0106 a0002c0007t0003g0107 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+503G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683389 | |||||||
| chr20:43683479 | C | A | 5 | a0001c0001t0001g0137 a0001c0001t0001g0147 a0001c0001t0001g0150 others(2): Show |
5 | HG02735.hp1 NA18965.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+593C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683479 | |||||||
| chr20:43683549 | G | GC | 13 | a0001c0001t0001g0105 a0001c0001t0001g0136 a0001c0001t0001g0139 others(10): Show |
13 | HG01175.hp2 HG01243.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.279+664dupC | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683549 | ||||||
| chr20:43683550 | C | CCT | 5 | a0003c0005t0001g0117 a0003c0005t0001g0118 a0003c0005t0001g0119 others(2): Show |
5 | HG00741.hp2 HG01167.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+664_279+665ins others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683550 | |||||||
| chr20:43683550 | CA | C | 5 | a0001c0001t0001g0126 a0001c0001t0001g0223 a0005c0008t0001g0112 others(2): Show |
5 | HG02486.hp1 HG02886.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+665delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683550 | |||||||
| chr20:43683551 | A | AT | 6 | a0001c0002t0001g0072 a0001c0002t0001g0100 a0002c0004t0001g0048 others(3): Show |
6 | HG00544.hp2 HG02056.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+685dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683551 | ||||||
| chr20:43683551 | A | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(130): Show |
140 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.279+665A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683551 | |||||||
| chr20:43683551 | A | T | 19 | a0001c0001t0001g0105 a0001c0001t0001g0136 a0001c0001t0001g0139 others(16): Show |
19 | HG00741.hp2 HG01167.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.279+665A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683551 | |||||||
| chr20:43683551 | AT | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(6): Show |
9 | HG01884.hp1 HG02630.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.279+685delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683551 | ||||||
| chr20:43683551 | ATT | A | 26 | a0001c0001t0002g0050 a0002c0003t0001g0003 a0002c0003t0001g0015 others(23): Show |
27 | HG01081.hp2 HG01361.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.279+684_279+685del others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683551 | ||||||
| chr20:43683551 | ATTT | A | 5 | a0002c0007t0001g0111 a0002c0007t0003g0107 a0002c0007t0003g0108 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+683_279+685del others(3): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683551 | ||||||
| chr20:43683551 | ATTTT | A | 6 | a0001c0017t0002g0124 a0004c0006t0002g0005 a0004c0006t0002g0101 others(3): Show |
7 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+682_279+685del others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683551 | ||||||
| chr20:43683552 | T | C | 5 | a0001c0001t0001g0126 a0001c0001t0001g0223 a0005c0008t0001g0112 others(2): Show |
5 | HG02486.hp1 HG02886.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+666T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683552 | |||||||
| chr20:43683607 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(1): Show |
4 | HG01884.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+721G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683607 | |||||||
| chr20:43683614 | C | T | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.279+728C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683614 | |||||||
| chr20:43683646 | C | T | 2 | a0001c0002t0001g0058 a0001c0002t0001g0094 |
2 | HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.279+760C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683646 | |||||||
| chr20:43683657 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): Show |
147 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.279+771G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683657 | |||||||
| chr20:43683664 | G | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(165): Show |
176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.279+778G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683664 | |||||||
| chr20:43683720 | A | AT | 6 | a0002c0007t0001g0111 a0002c0007t0003g0106 a0002c0007t0003g0107 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+841dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43683720 | ||||||
| chr20:43683782 | C | A | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(5): Show |
8 | HG01884.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+896C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683782 | |||||||
| chr20:43683843 | C | T | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.279+957C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683843 | |||||||
| chr20:43683979 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(165): Show |
176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.279+1093G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43683979 | |||||||
| chr20:43684013 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.279+1127C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684013 | |||||||
| chr20:43684038 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.279+1152C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684038 | |||||||
| chr20:43684052 | T | C | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.279+1166T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684052 | |||||||
| chr20:43684208 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(153): Show |
163 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.279+1322T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684208 | |||||||
| chr20:43684226 | C | CT | 36 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(33): Show |
37 | HG01081.hp2 HG01884.hp1 HG02083.hp2 others(34): Show |
intron_variant | MODIFIER | c.279+1353dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43684226 | ||||||
| chr20:43684276 | C | T | 1 | a0003c0005t0001g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.279+1390C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684276 | |||||||
| chr20:43684294 | A | G | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1408A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684294 | |||||||
| chr20:43684423 | G | A | 3 | a0002c0003t0001g0028 a0002c0003t0001g0034 a0002c0003t0001g0036 |
3 | HG01081.hp2 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.279+1537G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684423 | |||||||
| chr20:43684449 | C | G | 2 | a0001c0001t0001g0207 a0010c0012t0001g0243 |
2 | NA18992.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.279+1563C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684449 | |||||||
| chr20:43684515 | G | A | 21 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0045 others(18): Show |
21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+1629G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684515 | |||||||
| chr20:43684530 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.279+1644C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684530 | |||||||
| chr20:43684534 | C | CT | 42 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(39): Show |
44 | HG01081.hp2 HG01243.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.279+1665dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43684534 | ||||||
| chr20:43684534 | C | CTT | 8 | a0001c0017t0002g0124 a0002c0003t0001g0027 a0002c0007t0001g0111 others(5): Show |
8 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+1664_279+1665d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43684534 | ||||||
| chr20:43684615 | A | G | 21 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0045 others(18): Show |
21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+1729A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684615 | |||||||
| chr20:43684707 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02083.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.279+1821G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684707 | |||||||
| chr20:43684752 | G | C | 21 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0045 others(18): Show |
21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+1866G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684752 | |||||||
| chr20:43684770 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.279+1884G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684770 | |||||||
| chr20:43684774 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(221): Show |
233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.279+1888T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684774 | |||||||
| chr20:43684787 | C | T | 4 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0073 others(1): Show |
4 | HG00544.hp2 HG02027.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+1901C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684787 | |||||||
| chr20:43684801 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(221): Show |
233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.279+1915T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684801 | |||||||
| chr20:43684838 | TA | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(199): Show |
211 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.279+1965delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43684838 | ||||||
| chr20:43684850 | A | C | 4 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+1964A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684850 | |||||||
| chr20:43684854 | CAAAAG | C | 46 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(43): Show |
47 | HG01081.hp2 HG01109.hp2 HG02056.hp1 others(44): Show |
intron_variant | MODIFIER | c.279+1973_279+1977d others(7): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43684854 | ||||||
| chr20:43684912 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(221): Show |
233 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.280-1940T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684912 | |||||||
| chr20:43684980 | C | T | 21 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0045 others(18): Show |
21 | HG01109.hp2 HG02056.hp1 HG03041.hp2 others(18): Show |
intron_variant | MODIFIER | c.280-1872C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43684980 | |||||||
| chr20:43685059 | A | G | 3 | a0002c0003t0001g0003 a0002c0003t0001g0035 a0002c0003t0001g0037 |
4 | HG02486.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-1793A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685059 | |||||||
| chr20:43685108 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(140): Show |
150 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.280-1744T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685108 | |||||||
| chr20:43685147 | CA | C | 7 | a0001c0001t0001g0215 a0001c0017t0002g0124 a0004c0006t0002g0005 others(4): Show |
8 | HG01074.hp1 HG01243.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.280-1689delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43685147 | ||||||
| chr20:43685147 | CAA | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(149): Show |
159 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.280-1690_280-1689d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr20 | 43685147 | ||||||
| chr20:43685214 | C | G | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.280-1638C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685214 | |||||||
| chr20:43685427 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(165): Show |
176 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.280-1425T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685427 | |||||||
| chr20:43685456 | C | T | 3 | a0005c0008t0001g0112 a0005c0008t0001g0114 a0005c0008t0001g0116 |
3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.280-1396C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685456 | |||||||
| chr20:43685697 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.280-1155G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685697 | |||||||
| chr20:43685710 | G | A | 2 | a0001c0001t0001g0207 a0010c0012t0001g0243 |
2 | NA18992.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.280-1142G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685710 | |||||||
| chr20:43685916 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.280-936A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43685916 | |||||||
| chr20:43686069 | A | T | 2 | a0001c0001t0001g0207 a0010c0012t0001g0243 |
2 | NA18992.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.280-783A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686069 | |||||||
| chr20:43686263 | T | C | 6 | a0002c0007t0001g0111 a0002c0007t0003g0106 a0002c0007t0003g0107 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-589T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686263 | |||||||
| chr20:43686273 | G | A | 1 | a0001c0002t0001g0235 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.280-579G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686273 | |||||||
| chr20:43686349 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.280-503C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686349 | |||||||
| chr20:43686350 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.280-502G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686350 | |||||||
| chr20:43686371 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(140): Show |
150 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.280-481C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686371 | |||||||
| chr20:43686428 | G | C | 4 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-424G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686428 | |||||||
| chr20:43686451 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(199): Show |
211 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.280-401G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686451 | |||||||
| chr20:43686467 | T | C | 8 | a0003c0005t0001g0117 a0003c0005t0001g0118 a0003c0005t0001g0119 others(5): Show |
8 | HG00741.hp2 HG01167.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-385T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686467 | |||||||
| chr20:43686636 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.280-216T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686636 | |||||||
| chr20:43686640 | T | G | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.280-212T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686640 | |||||||
| chr20:43686652 | G | A | 1 | a0001c0002t0001g0094 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.280-200G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 4/13 | chr20 | 43686652 | |||||||
| chr20:43687254 | C | T | 1 | a0002c0003t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.500+182C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687254 | |||||||
| chr20:43687319 | C | T | 2 | a0002c0007t0003g0110 a0003c0005t0001g0119 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.500+247C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687319 | |||||||
| chr20:43687391 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.500+319T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687391 | |||||||
| chr20:43687434 | C | G | 1 | a0001c0002t0001g0070 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.500+362C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687434 | |||||||
| chr20:43687460 | A | C | 1 | a0001c0001t0001g0227 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.500+388A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687460 | |||||||
| chr20:43687770 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0127 a0001c0001t0001g0128 others(7): Show |
11 | HG00642.hp2 HG00741.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.500+698C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687770 | |||||||
| chr20:43687942 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(164): Show |
175 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.500+870G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687942 | |||||||
| chr20:43687998 | C | T | 13 | a0001c0001t0001g0008 a0001c0001t0001g0225 a0001c0001t0001g0226 others(10): Show |
14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.500+926C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43687998 | |||||||
| chr20:43688010 | C | CA | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(134): Show |
144 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.500+955dupA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43688010 | ||||||
| chr20:43688010 | C | CAA | 8 | a0001c0001t0001g0137 a0001c0001t0001g0196 a0001c0001t0001g0204 others(5): Show |
8 | HG02027.hp1 HG03225.hp2 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.500+954_500+955dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43688010 | ||||||
| chr20:43688047 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.500+975C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688047 | |||||||
| chr20:43688196 | T | G | 10 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.500+1124T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688196 | |||||||
| chr20:43688248 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.500+1176C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688248 | |||||||
| chr20:43688263 | G | A | 2 | a0001c0002t0001g0062 a0001c0002t0001g0093 |
2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.500+1191G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688263 | |||||||
| chr20:43688450 | C | T | 1 | a0001c0002t0001g0100 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.500+1378C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688450 | |||||||
| chr20:43688779 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(216): Show |
228 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.500+1707A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688779 | |||||||
| chr20:43688800 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): Show |
235 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(232): Show |
intron_variant | MODIFIER | c.500+1728T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688800 | |||||||
| chr20:43688812 | C | T | 49 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(46): Show |
50 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.500+1740C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688812 | |||||||
| chr20:43688851 | A | C | 4 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.500+1779A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43688851 | |||||||
| chr20:43689028 | G | T | 1 | a0002c0004t0001g0074 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.500+1956G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43689028 | |||||||
| chr20:43689043 | GGCCTCCC others(1786): Show |
G | 1 | a0001c0002t0001g0070 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.500+1979_501-1314d others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43689043 | ||||||
| chr20:43689118 | C | T | 10 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(7): Show |
10 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.500+2046C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43689118 | |||||||
| chr20:43689176 | C | G | 1 | a0002c0003t0001g0018 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.500+2104C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43689176 | |||||||
| chr20:43689892 | G | C | 7 | a0003c0005t0001g0117 a0003c0005t0001g0118 a0003c0005t0001g0119 others(4): Show |
7 | HG00741.hp2 HG01167.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.501-2265G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43689892 | |||||||
| chr20:43689961 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.501-2196G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43689961 | |||||||
| chr20:43690164 | C | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-1993C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690164 | |||||||
| chr20:43690192 | G | T | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.501-1965G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690192 | |||||||
| chr20:43690192 | GT | G | 58 | a0001c0001t0001g0137 a0001c0017t0002g0124 a0002c0003t0001g0003 others(55): Show |
60 | HG00741.hp2 HG01081.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.501-1952delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43690192 | ||||||
| chr20:43690194 | T | G | 6 | a0002c0007t0001g0111 a0002c0007t0003g0106 a0002c0007t0003g0107 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-1963T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690194 | |||||||
| chr20:43690202 | T | G | 32 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0125 others(29): Show |
35 | HG00544.hp2 HG01167.hp2 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.501-1955T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690202 | |||||||
| chr20:43690293 | C | T | 7 | a0001c0017t0002g0124 a0002c0007t0001g0111 a0002c0007t0003g0106 others(4): Show |
7 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.501-1864C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690293 | |||||||
| chr20:43690325 | C | G | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.501-1832C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690325 | |||||||
| chr20:43690362 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.501-1795C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690362 | |||||||
| chr20:43690366 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.501-1791T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690366 | |||||||
| chr20:43690735 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.501-1422A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690735 | |||||||
| chr20:43690873 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.501-1284C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690873 | |||||||
| chr20:43690876 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): Show |
235 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(232): Show |
intron_variant | MODIFIER | c.501-1281G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690876 | |||||||
| chr20:43690984 | C | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(223): Show |
235 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(232): Show |
intron_variant | MODIFIER | c.501-1173C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43690984 | |||||||
| chr20:43691229 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(1): Show |
4 | HG01884.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-928T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691229 | |||||||
| chr20:43691257 | G | C | 3 | a0001c0002t0001g0004 a0001c0002t0001g0068 a0001c0002t0001g0070 |
4 | NA18941.hp1 NA18945.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-900G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691257 | |||||||
| chr20:43691300 | A | T | 1 | a0001c0001t0001g0172 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.501-857A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691300 | |||||||
| chr20:43691308 | T | A | 29 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(26): Show |
31 | HG01081.hp2 HG01243.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.501-849T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691308 | |||||||
| chr20:43691309 | A | T | 1 | a0001c0001t0001g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.501-848A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691309 | |||||||
| chr20:43691313 | T | A | 6 | a0002c0007t0001g0111 a0002c0007t0003g0106 a0002c0007t0003g0107 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-844T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691313 | |||||||
| chr20:43691479 | G | A | 3 | a0002c0004t0001g0011 a0002c0004t0001g0012 a0002c0004t0001g0013 |
3 | HG02602.hp2 HG02615.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.501-678G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691479 | |||||||
| chr20:43691491 | C | A | 11 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(8): Show |
11 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.501-666C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691491 | |||||||
| chr20:43691492 | C | T | 11 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(8): Show |
11 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.501-665C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691492 | |||||||
| chr20:43691543 | A | AT | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(140): Show |
151 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.501-600dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43691543 | ||||||
| chr20:43691543 | A | ATT | 9 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0143 others(6): Show |
9 | HG01109.hp1 HG01952.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-601_501-600dup others(2): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43691543 | ||||||
| chr20:43691566 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.501-591A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691566 | |||||||
| chr20:43691603 | C | T | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0251 others(1): Show |
4 | HG01891.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-554C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691603 | |||||||
| chr20:43691639 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.501-518A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691639 | |||||||
| chr20:43691768 | A | G | 1 | a0002c0003t0001g0031 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.501-389A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691768 | |||||||
| chr20:43691785 | C | T | 1 | a0009c0010t0001g0054 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.501-372C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691785 | |||||||
| chr20:43691842 | A | AT | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.501-300dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr20 | 43691842 | ||||||
| chr20:43691970 | T | C | 12 | a0001c0017t0002g0124 a0002c0007t0001g0111 a0002c0007t0003g0106 others(9): Show |
13 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.501-187T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 5/13 | chr20 | 43691970 | |||||||
| chr20:43692582 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(217): Show |
229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.663+263A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43692582 | |||||||
| chr20:43692982 | A | G | 1 | a0003c0005t0001g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.663+663A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43692982 | |||||||
| chr20:43693011 | T | C | 6 | a0002c0007t0001g0111 a0002c0007t0003g0106 a0002c0007t0003g0107 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.663+692T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43693011 | |||||||
| chr20:43693188 | C | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(216): Show |
228 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.663+869C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43693188 | |||||||
| chr20:43693579 | C | T | 1 | a0002c0004t0001g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.663+1260C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43693579 | |||||||
| chr20:43693948 | T | TGAGGTGG others(19): Show |
1 | a0002c0004t0001g0087 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.663+1640_663+1665d others(28): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43693948 | ||||||
| chr20:43693991 | T | G | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.663+1672T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43693991 | |||||||
| chr20:43694071 | G | T | 6 | a0002c0007t0001g0111 a0002c0007t0003g0106 a0002c0007t0003g0107 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.663+1752G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694071 | |||||||
| chr20:43694115 | G | A | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663+1796G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694115 | |||||||
| chr20:43694245 | T | G | 1 | a0002c0003t0001g0217 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.663+1926T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694245 | |||||||
| chr20:43694294 | T | G | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663+1975T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694294 | |||||||
| chr20:43694325 | C | G | 1 | a0001c0001t0001g0229 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.663+2006C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694325 | |||||||
| chr20:43694343 | A | G | 2 | a0001c0002t0001g0058 a0001c0002t0001g0094 |
2 | HG01099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.663+2024A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694343 | |||||||
| chr20:43694373 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.663+2054T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694373 | |||||||
| chr20:43694394 | A | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(217): Show |
229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.663+2075A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694394 | |||||||
| chr20:43694396 | T | TTA | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(217): Show |
229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.663+2077_663+2078i others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694396 | |||||||
| chr20:43694414 | C | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(217): Show |
229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.663+2095C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694414 | |||||||
| chr20:43694530 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.663+2211G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694530 | |||||||
| chr20:43694699 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.663+2380G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694699 | |||||||
| chr20:43694843 | C | T | 1 | a0002c0004t0001g0047 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.663+2524C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43694843 | |||||||
| chr20:43695037 | A | AT | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(216): Show |
228 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.663+2733dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43695037 | ||||||
| chr20:43695095 | G | A | 1 | a0004c0006t0002g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.663+2776G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695095 | |||||||
| chr20:43695190 | C | T | 1 | a0002c0004t0001g0074 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.663+2871C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695190 | |||||||
| chr20:43695191 | G | A | 24 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(21): Show |
25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.663+2872G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695191 | |||||||
| chr20:43695240 | C | T | 16 | a0001c0017t0002g0124 a0002c0003t0001g0014 a0002c0003t0001g0015 others(13): Show |
17 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.663+2921C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695240 | |||||||
| chr20:43695382 | T | C | 1 | a0002c0004t0001g0076 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.663+3063T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695382 | |||||||
| chr20:43695427 | A | G | 3 | a0002c0003t0001g0003 a0002c0003t0001g0035 a0002c0003t0001g0037 |
4 | HG02486.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.663+3108A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695427 | |||||||
| chr20:43695466 | T | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(1): Show |
4 | HG01884.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.663+3147T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695466 | |||||||
| chr20:43695550 | G | A | 1 | a0002c0003t0001g0031 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.663+3231G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695550 | |||||||
| chr20:43695578 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(201): Show |
212 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.663+3259A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695578 | |||||||
| chr20:43695594 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.663+3275G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695594 | |||||||
| chr20:43695617 | C | G | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663+3298C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695617 | |||||||
| chr20:43695686 | CA | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(217): Show |
229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.663+3381delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43695686 | ||||||
| chr20:43695695 | A | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(137): Show |
147 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.663+3376A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695695 | |||||||
| chr20:43695752 | A | AG | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(138): Show |
148 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.663+3435dupG | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43695752 | ||||||
| chr20:43695767 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.663+3448G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695767 | |||||||
| chr20:43695902 | C | G | 1 | a0002c0004t0001g0081 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.663+3583C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695902 | |||||||
| chr20:43695950 | G | A | 1 | a0001c0002t0001g0058 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.663+3631G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695950 | |||||||
| chr20:43695977 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.663+3658T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43695977 | |||||||
| chr20:43696095 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.664-3662G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696095 | |||||||
| chr20:43696107 | A | T | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.664-3650A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696107 | |||||||
| chr20:43696243 | CT | C | 11 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(8): Show |
11 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.664-3500delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43696243 | ||||||
| chr20:43696263 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.664-3494G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696263 | |||||||
| chr20:43696484 | A | G | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.664-3273A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696484 | |||||||
| chr20:43696486 | A | ACTGGGAT others(1001): Show |
4 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.664-2994_664-2993i others(1010): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43696486 | ||||||
| chr20:43696486 | A | ACTGGGAT others(497): Show |
40 | a0002c0003t0001g0003 a0002c0003t0001g0019 a0002c0003t0001g0020 others(37): Show |
41 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(38): Show |
intron_variant | MODIFIER | c.664-2907_664-2906i others(506): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43696486 | ||||||
| chr20:43696486 | A | ACTGGGAT others(498): Show |
139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(136): Show |
146 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.664-3017_664-3016i others(507): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43696486 | ||||||
| chr20:43696764 | G | C | 16 | a0001c0017t0002g0124 a0002c0003t0001g0014 a0002c0003t0001g0015 others(13): Show |
17 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.664-2993G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696764 | |||||||
| chr20:43696851 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(217): Show |
229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.664-2906T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696851 | |||||||
| chr20:43696972 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.664-2785G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43696972 | |||||||
| chr20:43697021 | G | A | 5 | a0002c0004t0001g0012 a0002c0004t0001g0013 a0005c0008t0001g0112 others(2): Show |
5 | HG02486.hp1 HG02602.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-2736G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697021 | |||||||
| chr20:43697180 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.664-2577G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697180 | |||||||
| chr20:43697424 | A | G | 11 | a0003c0005t0001g0115 a0003c0005t0001g0117 a0003c0005t0001g0118 others(8): Show |
11 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.664-2333A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697424 | |||||||
| chr20:43697593 | A | T | 1 | a0003c0005t0001g0118 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.664-2164A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697593 | |||||||
| chr20:43697661 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.664-2096T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697661 | |||||||
| chr20:43697784 | G | A | 1 | a0002c0004t0001g0011 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.664-1973G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697784 | |||||||
| chr20:43697875 | A | G | 4 | a0002c0007t0001g0111 a0002c0007t0003g0108 a0002c0007t0003g0109 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.664-1882A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697875 | |||||||
| chr20:43697891 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.664-1866G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697891 | |||||||
| chr20:43697900 | G | A | 1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.664-1857G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697900 | |||||||
| chr20:43697914 | C | CA | 31 | a0001c0001t0001g0192 a0001c0001t0001g0196 a0001c0001t0001g0216 others(28): Show |
32 | HG01081.hp2 HG01175.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.664-1825dupA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43697914 | ||||||
| chr20:43697914 | C | CAA | 11 | a0001c0017t0002g0124 a0002c0007t0001g0111 a0002c0007t0003g0106 others(8): Show |
12 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.664-1826_664-1825d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43697914 | ||||||
| chr20:43697937 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(217): Show |
229 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(226): Show |
intron_variant | MODIFIER | c.664-1820G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43697937 | |||||||
| chr20:43698061 | CT | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
136 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.664-1677delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698061 | ||||||
| chr20:43698061 | CTT | C | 20 | a0002c0003t0001g0018 a0002c0003t0001g0019 a0002c0003t0001g0020 others(17): Show |
20 | HG02083.hp2 HG02486.hp1 HG02886.hp1 others(17): Show |
intron_variant | MODIFIER | c.664-1678_664-1677d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698061 | ||||||
| chr20:43698080 | T | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(204): Show |
215 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.664-1677T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698080 | |||||||
| chr20:43698080 | T | TG | 7 | a0001c0001t0001g0239 a0002c0007t0001g0111 a0002c0007t0003g0106 others(4): Show |
7 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-1677_664-1676i others(3): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698080 | |||||||
| chr20:43698080 | T | TTG | 4 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0103 others(1): Show |
5 | HG02055.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-1677_664-1676i others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698080 | |||||||
| chr20:43698240 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(138): Show |
148 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.664-1517A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698240 | |||||||
| chr20:43698258 | C | T | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-1499C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698258 | |||||||
| chr20:43698347 | G | A | 1 | a0002c0004t0001g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.664-1410G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698347 | |||||||
| chr20:43698349 | A | G | 1 | a0002c0004t0001g0083 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.664-1408A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698349 | |||||||
| chr20:43698351 | A | ATTTTTTT others(6): Show |
1 | a0001c0002t0001g0093 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.664-1374_664-1362d others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | ||||||
| chr20:43698351 | A | ATTTTTTT others(13): Show |
2 | a0001c0002t0001g0062 a0001c0002t0001g0066 |
2 | HG03516.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.664-1381_664-1362d others(22): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | ||||||
| chr20:43698351 | ATTTT | A | 5 | a0001c0002t0001g0055 a0001c0002t0001g0058 a0001c0002t0001g0060 others(2): Show |
5 | HG01099.hp2 HG02257.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.664-1365_664-1362d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | ||||||
| chr20:43698351 | ATTTTTTT others(3): Show |
A | 8 | a0001c0002t0001g0010 a0001c0002t0001g0068 a0001c0002t0001g0070 others(5): Show |
9 | HG01934.hp2 HG01952.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.664-1371_664-1362d others(12): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | ||||||
| chr20:43698351 | ATTTTTTT others(4): Show |
A | 5 | a0001c0002t0001g0009 a0001c0002t0001g0071 a0001c0002t0001g0072 others(2): Show |
6 | HG00544.hp2 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-1372_664-1362d others(13): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | ||||||
| chr20:43698351 | ATTTTTTT others(6): Show |
A | 1 | a0001c0002t0001g0067 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.664-1374_664-1362d others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | ||||||
| chr20:43698351 | ATTTTTTT others(8): Show |
A | 12 | a0001c0001t0001g0043 a0002c0003t0001g0014 a0002c0003t0001g0015 others(9): Show |
12 | HG01361.hp2 HG02615.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.664-1376_664-1362d others(17): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | ||||||
| chr20:43698351 | ATTTTTTT others(9): Show |
A | 20 | a0001c0001t0001g0052 a0001c0001t0001g0088 a0001c0001t0001g0187 others(17): Show |
20 | HG01261.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.664-1377_664-1362d others(18): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | ||||||
| chr20:43698351 | ATTTTTTT others(10): Show |
A | 60 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0127 others(57): Show |
61 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.664-1378_664-1362d others(19): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | ||||||
| chr20:43698351 | ATTTTTTT others(12): Show |
A | 37 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0140 others(34): Show |
38 | HG00544.hp1 HG00642.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.664-1380_664-1362d others(21): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | ||||||
| chr20:43698351 | ATTTTTTT others(13): Show |
A | 1 | a0001c0011t0001g0257 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.664-1381_664-1362d others(22): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698351 | ||||||
| chr20:43698414 | G | A | 12 | a0001c0017t0002g0124 a0002c0007t0001g0111 a0002c0007t0003g0106 others(9): Show |
13 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.664-1343G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698414 | |||||||
| chr20:43698446 | C | T | 1 | a0002c0004t0001g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.664-1311C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698446 | |||||||
| chr20:43698661 | A | AT | 7 | a0001c0001t0001g0138 a0001c0001t0001g0216 a0001c0001t0001g0223 others(4): Show |
7 | HG02056.hp2 HG02071.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.664-1074dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698661 | ||||||
| chr20:43698661 | AT | A | 59 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(56): Show |
61 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.664-1074delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698661 | ||||||
| chr20:43698661 | ATTT | A | 21 | a0001c0001t0002g0050 a0002c0003t0001g0014 a0002c0003t0001g0015 others(18): Show |
21 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.664-1076_664-1074d others(5): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43698661 | ||||||
| chr20:43698809 | C | T | 2 | a0001c0002t0001g0091 a0001c0002t0001g0092 |
2 | HG01993.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.664-948C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698809 | |||||||
| chr20:43698872 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.664-885G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698872 | |||||||
| chr20:43698927 | T | C | 1 | a0002c0003t0001g0016 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.664-830T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43698927 | |||||||
| chr20:43699036 | A | T | 1 | a0001c0001t0002g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.664-721A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699036 | |||||||
| chr20:43699080 | C | G | 1 | a0001c0002t0001g0235 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.664-677C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699080 | |||||||
| chr20:43699107 | C | T | 1 | a0001c0002t0001g0090 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.664-650C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699107 | |||||||
| chr20:43699130 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.664-627C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699130 | |||||||
| chr20:43699163 | C | T | 1 | a0001c0002t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.664-594C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699163 | |||||||
| chr20:43699169 | G | A | 1 | a0002c0004t0001g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.664-588G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699169 | |||||||
| chr20:43699205 | ATTTTG | A | 7 | a0001c0017t0002g0124 a0002c0007t0001g0111 a0002c0007t0003g0106 others(4): Show |
7 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.664-537_664-533del others(5): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr20 | 43699205 | ||||||
| chr20:43699214 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.664-543T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699214 | |||||||
| chr20:43699246 | A | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0159 a0001c0001t0001g0160 others(10): Show |
14 | HG00642.hp2 HG00741.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.664-511A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699246 | |||||||
| chr20:43699325 | C | T | 3 | a0005c0008t0001g0112 a0005c0008t0001g0114 a0005c0008t0001g0116 |
3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.664-432C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699325 | |||||||
| chr20:43699340 | C | T | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.664-417C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699340 | |||||||
| chr20:43699444 | T | C | 1 | a0002c0003t0001g0032 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.664-313T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699444 | |||||||
| chr20:43699582 | G | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(222): Show |
234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.664-175G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699582 | |||||||
| chr20:43699590 | G | A | 12 | a0001c0017t0002g0124 a0002c0007t0001g0111 a0002c0007t0003g0106 others(9): Show |
13 | HG01243.hp1 HG01361.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.664-167G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 6/13 | chr20 | 43699590 | |||||||
| chr20:43700109 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(220): Show |
232 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(229): Show |
intron_variant | MODIFIER | c.951+65A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700109 | |||||||
| chr20:43700136 | C | T | 44 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0133 others(41): Show |
45 | HG00544.hp1 HG00642.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.951+92C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700136 | |||||||
| chr20:43700240 | C | T | 49 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(46): Show |
50 | HG01081.hp1 HG01081.hp2 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.951+196C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700240 | |||||||
| chr20:43700292 | G | A | 3 | a0005c0008t0001g0112 a0005c0008t0001g0114 a0005c0008t0001g0116 |
3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.951+248G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700292 | |||||||
| chr20:43700453 | G | A | 17 | a0002c0003t0001g0018 a0002c0003t0001g0019 a0002c0003t0001g0020 others(14): Show |
17 | HG02083.hp2 HG03491.hp2 HG03492.hp2 others(14): Show |
intron_variant | MODIFIER | c.951+409G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700453 | |||||||
| chr20:43700594 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.951+550C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700594 | |||||||
| chr20:43700719 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.951+675G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700719 | |||||||
| chr20:43700803 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.951+759A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700803 | |||||||
| chr20:43700979 | C | T | 1 | a0001c0002t0001g0066 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.951+935C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43700979 | |||||||
| chr20:43701082 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.951+1038C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701082 | |||||||
| chr20:43701159 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(136): Show |
146 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.951+1115C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701159 | |||||||
| chr20:43701283 | TTC | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0063 others(26): Show |
31 | HG00280.hp2 HG00673.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.952-1205_952-1204d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr20 | 43701283 | ||||||
| chr20:43701297 | A | G | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.952-1193A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701297 | |||||||
| chr20:43701305 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(216): Show |
228 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.952-1185G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701305 | |||||||
| chr20:43701324 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(222): Show |
234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.952-1166A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701324 | |||||||
| chr20:43701430 | A | G | 1 | a0001c0002t0001g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.952-1060A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701430 | |||||||
| chr20:43701628 | AG | A | 3 | a0005c0008t0001g0112 a0005c0008t0001g0114 a0005c0008t0001g0116 |
3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.952-861delG | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701628 | |||||||
| chr20:43701718 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.952-772C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701718 | |||||||
| chr20:43701936 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(216): Show |
228 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.952-554T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701936 | |||||||
| chr20:43701991 | G | T | 2 | a0002c0004t0001g0083 a0002c0004t0001g0087 |
2 | NA18939.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.952-499G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43701991 | |||||||
| chr20:43702300 | T | C | 24 | a0002c0003t0001g0217 a0002c0004t0001g0011 a0002c0004t0001g0041 others(21): Show |
24 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(21): Show |
intron_variant | MODIFIER | c.952-190T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43702300 | |||||||
| chr20:43702344 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.952-146G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43702344 | |||||||
| chr20:43702413 | A | C | 3 | a0005c0008t0001g0112 a0005c0008t0001g0114 a0005c0008t0001g0116 |
3 | HG02486.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.952-77A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 7/13 | chr20 | 43702413 | |||||||
| chr20:43702906 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG01433.hp2 | splice_region_variant&intron_variant | LOW | c.1365+3G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43702906 | |||||||
| chr20:43702931 | T | C | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1365+28T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43702931 | |||||||
| chr20:43702937 | C | G | 1 | a0001c0002t0001g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1365+34C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43702937 | |||||||
| chr20:43703206 | C | T | 68 | a0002c0003t0001g0003 a0002c0003t0001g0014 a0002c0003t0001g0015 others(65): Show |
69 | HG00741.hp2 HG01081.hp1 HG01081.hp2 others(66): Show |
intron_variant | MODIFIER | c.1365+303C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703206 | |||||||
| chr20:43703249 | CA | C | 26 | a0002c0003t0001g0217 a0002c0004t0001g0011 a0002c0004t0001g0012 others(23): Show |
26 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.1365+349delA | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43703249 | ||||||
| chr20:43703254 | A | G | 18 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(15): Show |
18 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1365+351A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703254 | |||||||
| chr20:43703310 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(1): Show |
4 | HG01884.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+407C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703310 | |||||||
| chr20:43703414 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1365+511C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703414 | |||||||
| chr20:43703414 | C | G | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1365+511C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703414 | |||||||
| chr20:43703442 | G | T | 24 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(21): Show |
25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.1365+539G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703442 | |||||||
| chr20:43703446 | C | A | 4 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+543C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703446 | |||||||
| chr20:43703700 | C | T | 4 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0066 others(1): Show |
4 | HG01978.hp2 HG02056.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+797C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703700 | |||||||
| chr20:43703814 | CCA | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(1): Show |
4 | HG01884.hp1 HG02630.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+914_1365+915d others(4): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr20 | 43703814 | ||||||
| chr20:43703913 | G | A | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1365+1010G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43703913 | |||||||
| chr20:43704070 | G | C | 1 | a0010c0012t0001g0243 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1366-1149G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704070 | |||||||
| chr20:43704112 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1366-1107C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704112 | |||||||
| chr20:43704142 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(222): Show |
234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.1366-1077C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704142 | |||||||
| chr20:43704222 | G | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0049 a0001c0001t0001g0063 others(4): Show |
9 | HG00673.hp2 HG02071.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366-997G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704222 | |||||||
| chr20:43704380 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1366-839G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704380 | |||||||
| chr20:43704519 | G | A | 1 | a0001c0002t0001g0235 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1366-700G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704519 | |||||||
| chr20:43704610 | G | C | 1 | a0002c0007t0003g0107 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1366-609G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704610 | |||||||
| chr20:43704611 | C | G | 22 | a0002c0003t0001g0217 a0002c0004t0001g0012 a0002c0004t0001g0013 others(19): Show |
22 | HG01081.hp1 HG02056.hp1 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.1366-608C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704611 | |||||||
| chr20:43704653 | C | G | 26 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0017t0002g0124 others(23): Show |
27 | HG00741.hp2 HG01167.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1366-566C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704653 | |||||||
| chr20:43704785 | A | C | 3 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0017t0002g0124 |
3 | HG02723.hp2 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1366-434A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704785 | |||||||
| chr20:43704827 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0245 |
3 | HG01884.hp2 HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1366-392C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43704827 | |||||||
| chr20:43705036 | C | G | 15 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(12): Show |
15 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1366-183C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 8/13 | chr20 | 43705036 | |||||||
| chr20:43705426 | G | A | 1 | a0001c0001t0004g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1505+68G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705426 | |||||||
| chr20:43705530 | G | A | 73 | a0001c0017t0002g0124 a0002c0003t0001g0003 a0002c0003t0001g0018 others(70): Show |
75 | HG00741.hp2 HG01081.hp1 HG01081.hp2 others(72): Show |
intron_variant | MODIFIER | c.1505+172G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705530 | |||||||
| chr20:43705567 | T | G | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505+209T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705567 | |||||||
| chr20:43705576 | T | G | 6 | a0001c0017t0002g0124 a0004c0006t0002g0005 a0004c0006t0002g0101 others(3): Show |
7 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1505+218T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705576 | |||||||
| chr20:43705672 | A | ATATT | 25 | a0001c0001t0001g0044 a0001c0001t0001g0145 a0001c0001t0001g0152 others(22): Show |
25 | HG00280.hp1 HG00642.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1505+356_1505+359d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | ||||||
| chr20:43705672 | A | ATATTTAT others(1): Show |
9 | a0001c0001t0001g0043 a0001c0001t0001g0153 a0001c0001t0001g0208 others(6): Show |
9 | HG01261.hp2 HG01361.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1505+352_1505+359d others(10): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | ||||||
| chr20:43705672 | A | ATATTTAT others(5): Show |
3 | a0001c0001t0001g0175 a0001c0017t0002g0124 a0003c0005t0001g0117 |
3 | HG01167.hp1 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1505+348_1505+359d others(14): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | ||||||
| chr20:43705672 | ATATT | A | 5 | a0001c0001t0001g0052 a0001c0001t0001g0088 a0001c0001t0001g0212 others(2): Show |
5 | HG01884.hp1 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1505+356_1505+359d others(6): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | ||||||
| chr20:43705672 | ATATTTAT others(1): Show |
A | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505+352_1505+359d others(10): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | ||||||
| chr20:43705672 | ATATTTAT others(13): Show |
A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1505+340_1505+359d others(22): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43705672 | ||||||
| chr20:43705815 | C | T | 1 | a0001c0002t0001g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1505+457C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705815 | |||||||
| chr20:43705826 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1505+468G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705826 | |||||||
| chr20:43705857 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1505+499C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705857 | |||||||
| chr20:43705938 | G | C | 4 | a0002c0007t0001g0111 a0005c0008t0001g0112 a0005c0008t0001g0114 others(1): Show |
4 | HG02486.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1505+580G>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43705938 | |||||||
| chr20:43706003 | A | G | 1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1505+645A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706003 | |||||||
| chr20:43706193 | C | T | 1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1505+835C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706193 | |||||||
| chr20:43706269 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0088 |
2 | HG01884.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1505+911A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706269 | |||||||
| chr20:43706402 | G | A | 4 | a0002c0007t0001g0111 a0005c0008t0001g0112 a0005c0008t0001g0114 others(1): Show |
4 | HG02486.hp1 HG02886.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1505+1044G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706402 | |||||||
| chr20:43706462 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1505+1104A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706462 | |||||||
| chr20:43706707 | A | C | 7 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0200 others(4): Show |
7 | HG00738.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1505+1349A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706707 | |||||||
| chr20:43706716 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0195 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1505+1358_1505+135 others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706716 | |||||||
| chr20:43706717 | A | AGTGTTTT others(5): Show |
1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1505+1359_1505+136 others(16): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | AGTTT | 7 | a0003c0005t0001g0117 a0003c0005t0001g0118 a0003c0005t0001g0119 others(4): Show |
7 | HG00741.hp2 HG01167.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(8): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | AGTTTT | 23 | a0002c0004t0001g0012 a0002c0004t0001g0041 a0002c0004t0001g0045 others(20): Show |
23 | HG01081.hp1 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(9): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | AGTTTTT | 6 | a0002c0003t0001g0217 a0002c0004t0001g0011 a0002c0004t0001g0013 others(3): Show |
6 | HG02615.hp2 HG02738.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(10): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | AGTTTTTT others(5): Show |
1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1505+1359_1505+136 others(16): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | AGTTTTTT others(3): Show |
3 | a0002c0003t0001g0014 a0002c0003t0001g0016 a0002c0003t0001g0017 |
3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(14): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | AGTTTTTT others(4): Show |
6 | a0002c0003t0001g0015 a0002c0003t0001g0023 a0002c0003t0001g0029 others(3): Show |
6 | HG02717.hp2 NA18952.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | AGTTTTTT others(5): Show |
13 | a0002c0003t0001g0018 a0002c0003t0001g0019 a0002c0003t0001g0020 others(10): Show |
13 | HG01361.hp2 HG02083.hp2 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(16): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | AGTTTTTT others(6): Show |
9 | a0002c0003t0001g0003 a0002c0003t0001g0022 a0002c0003t0001g0028 others(6): Show |
10 | HG01081.hp2 HG02486.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(17): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | AGTTTTTT others(7): Show |
2 | a0002c0003t0001g0037 a0002c0003t0001g0040 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(18): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | ATTTT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0129 a0001c0001t0001g0166 others(3): Show |
8 | HG02027.hp1 NA18612.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(8): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0227 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1505+1359_1505+136 others(14): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | ATTTTTTT others(4): Show |
19 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0177 others(16): Show |
19 | HG00738.hp2 HG01099.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(15): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | ATTTTTTT others(5): Show |
77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(74): Show |
81 | HG00280.hp2 HG00544.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(16): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | ATTTTTTT others(6): Show |
27 | a0001c0001t0001g0008 a0001c0001t0001g0125 a0001c0001t0001g0130 others(24): Show |
28 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(17): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | ATTTTTTT others(7): Show |
6 | a0001c0001t0001g0138 a0001c0001t0001g0157 a0001c0001t0001g0160 others(3): Show |
6 | HG00738.hp1 HG01261.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1505+1359_1505+136 others(18): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706717 | A | T | 1 | a0001c0001t0001g0195 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1505+1359A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706717 | |||||||
| chr20:43706718 | A | AAGTTTTT others(3): Show |
2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1505+1360_1505+136 others(14): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706718 | |||||||
| chr20:43706718 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0150 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1505+1360_1505+136 others(18): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706718 | |||||||
| chr20:43706718 | A | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(206): Show |
217 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(214): Show |
intron_variant | MODIFIER | c.1505+1360A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706718 | |||||||
| chr20:43706719 | G | GTTTTTTT others(6): Show |
3 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0103 |
4 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1505+1363_1505+137 others(17): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43706719 | ||||||
| chr20:43706719 | G | GTTTTTTT others(7): Show |
3 | a0004c0006t0002g0102 a0004c0006t0002g0104 a0005c0008t0001g0116 |
3 | HG01243.hp1 HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1505+1362_1505+137 others(18): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43706719 | ||||||
| chr20:43706719 | G | GTTTTTTT others(8): Show |
1 | a0002c0007t0001g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1505+1375_1505+137 others(19): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43706719 | ||||||
| chr20:43706719 | G | GTTTTTTT others(9): Show |
2 | a0005c0008t0001g0112 a0005c0008t0001g0114 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1505+1375_1505+137 others(20): Show |
MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43706719 | ||||||
| chr20:43706719 | G | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(209): Show |
220 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(217): Show |
intron_variant | MODIFIER | c.1505+1361G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706719 | |||||||
| chr20:43706743 | T | C | 6 | a0001c0001t0001g0125 a0001c0001t0001g0156 a0001c0001t0001g0183 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1505+1385T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706743 | |||||||
| chr20:43706904 | C | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0174 |
2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1505+1546C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706904 | |||||||
| chr20:43706916 | G | A | 5 | a0002c0007t0003g0106 a0002c0007t0003g0107 a0002c0007t0003g0108 others(2): Show |
5 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1505+1558G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706916 | |||||||
| chr20:43706925 | A | C | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1505+1567A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43706925 | |||||||
| chr20:43707040 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(185): Show |
196 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.1505+1682C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707040 | |||||||
| chr20:43707181 | G | GT | 7 | a0002c0003t0001g0003 a0002c0003t0001g0028 a0002c0003t0001g0034 others(4): Show |
8 | HG01081.hp2 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1505+1837dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43707181 | ||||||
| chr20:43707181 | GT | G | 41 | a0001c0001t0001g0007 a0001c0001t0001g0088 a0001c0001t0001g0105 others(38): Show |
42 | HG00544.hp1 HG00642.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1505+1837delT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43707181 | ||||||
| chr20:43707194 | T | A | 1 | a0002c0004t0001g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1505+1836T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707194 | |||||||
| chr20:43707195 | T | A | 35 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0002c0003t0001g0014 others(32): Show |
36 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1505+1837T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707195 | |||||||
| chr20:43707196 | A | T | 25 | a0001c0001t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0019 others(22): Show |
25 | HG01361.hp2 HG02083.hp2 HG02615.hp1 others(22): Show |
intron_variant | MODIFIER | c.1505+1838A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707196 | |||||||
| chr20:43707197 | A | T | 1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1505+1839A>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707197 | |||||||
| chr20:43707263 | C | G | 1 | a0001c0001t0001g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1505+1905C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707263 | |||||||
| chr20:43707565 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(135): Show |
145 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1505+2207C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707565 | |||||||
| chr20:43707640 | C | T | 72 | a0001c0017t0002g0124 a0002c0003t0001g0003 a0002c0003t0001g0014 others(69): Show |
73 | HG00741.hp2 HG01081.hp1 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.1505+2282C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707640 | |||||||
| chr20:43707768 | T | C | 1 | a0002c0004t0001g0011 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1506-2195T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707768 | |||||||
| chr20:43707898 | G | A | 4 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-2065G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707898 | |||||||
| chr20:43707959 | T | C | 1 | a0001c0002t0001g0060 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1506-2004T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43707959 | |||||||
| chr20:43708044 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(135): Show |
145 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1506-1919C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708044 | |||||||
| chr20:43708314 | A | G | 1 | a0008c0016t0003g0252 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1506-1649A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708314 | |||||||
| chr20:43708317 | C | T | 1 | a0001c0002t0001g0100 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1506-1646C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708317 | |||||||
| chr20:43708377 | G | A | 6 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0045 others(3): Show |
6 | NA18946.hp2 NA18963.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506-1586G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708377 | |||||||
| chr20:43708388 | C | A | 4 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-1575C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708388 | |||||||
| chr20:43708434 | C | CT | 4 | a0001c0001t0001g0125 a0001c0001t0001g0183 a0001c0001t0001g0195 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-1521dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43708434 | ||||||
| chr20:43708495 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1506-1468G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708495 | |||||||
| chr20:43708783 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0150 a0001c0001t0001g0213 others(1): Show |
4 | NA18965.hp2 NA18990.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506-1180G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708783 | |||||||
| chr20:43708847 | C | G | 4 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0251 others(1): Show |
4 | HG01891.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-1116C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708847 | |||||||
| chr20:43708919 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG02083.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1506-1044C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708919 | |||||||
| chr20:43708947 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1506-1016G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708947 | |||||||
| chr20:43708976 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1506-987G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708976 | |||||||
| chr20:43708991 | A | G | 5 | a0002c0007t0003g0106 a0002c0007t0003g0107 a0002c0007t0003g0108 others(2): Show |
5 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506-972A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43708991 | |||||||
| chr20:43709126 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1506-837C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709126 | |||||||
| chr20:43709134 | AG | A | 4 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-827delG | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr20 | 43709134 | ||||||
| chr20:43709235 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(135): Show |
145 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1506-728C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709235 | |||||||
| chr20:43709297 | A | C | 2 | a0001c0002t0001g0057 a0001c0013t0001g0053 |
2 | NA18612.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1506-666A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709297 | |||||||
| chr20:43709503 | T | A | 1 | a0001c0001t0001g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1506-460T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709503 | |||||||
| chr20:43709504 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1506-459C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709504 | |||||||
| chr20:43709648 | C | A | 5 | a0002c0007t0003g0106 a0002c0007t0003g0107 a0002c0007t0003g0108 others(2): Show |
5 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506-315C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 9/13 | chr20 | 43709648 | |||||||
| chr20:43710078 | G | A | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1605+16G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710078 | |||||||
| chr20:43710415 | C | A | 1 | a0001c0017t0002g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1605+353C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710415 | |||||||
| chr20:43710551 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1605+489T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710551 | |||||||
| chr20:43710671 | G | T | 1 | a0002c0007t0003g0106 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1605+609G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710671 | |||||||
| chr20:43710878 | G | A | 1 | a0002c0004t0001g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1606-610G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710878 | |||||||
| chr20:43710963 | T | G | 1 | a0001c0002t0001g0090 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1606-525T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43710963 | |||||||
| chr20:43711053 | C | T | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1606-435C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711053 | |||||||
| chr20:43711142 | G | A | 1 | a0001c0011t0001g0257 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1606-346G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711142 | |||||||
| chr20:43711149 | T | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1606-339T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711149 | |||||||
| chr20:43711185 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1606-303C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711185 | |||||||
| chr20:43711233 | G | T | 1 | a0001c0002t0001g0235 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1606-255G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711233 | |||||||
| chr20:43711254 | G | A | 24 | a0002c0003t0001g0003 a0002c0003t0001g0018 a0002c0003t0001g0019 others(21): Show |
25 | HG01081.hp2 HG02083.hp2 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.1606-234G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711254 | |||||||
| chr20:43711314 | C | G | 1 | a0003c0005t0001g0117 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1606-174C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711314 | |||||||
| chr20:43711416 | TG | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0245 |
3 | HG01884.hp2 HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1606-70delG | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr20 | 43711416 | ||||||
| chr20:43711474 | G | A | 6 | a0001c0017t0002g0124 a0004c0006t0002g0005 a0004c0006t0002g0101 others(3): Show |
7 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1606-14G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 10/13 | chr20 | 43711474 | |||||||
| chr20:43711773 | A | G | 1 | a0001c0002t0001g0235 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1719+172A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43711773 | |||||||
| chr20:43711886 | C | T | 1 | a0002c0004t0001g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1719+285C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43711886 | |||||||
| chr20:43711923 | G | T | 4 | a0002c0007t0003g0107 a0002c0007t0003g0108 a0002c0007t0003g0109 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1719+322G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43711923 | |||||||
| chr20:43711993 | G | A | 1 | a0002c0007t0003g0106 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1719+392G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43711993 | |||||||
| chr20:43712022 | G | A | 26 | a0002c0003t0001g0217 a0002c0004t0001g0011 a0002c0004t0001g0012 others(23): Show |
26 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.1719+421G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712022 | |||||||
| chr20:43712044 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(135): Show |
145 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1719+443G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712044 | |||||||
| chr20:43712344 | G | A | 5 | a0002c0007t0003g0106 a0002c0007t0003g0107 a0002c0007t0003g0108 others(2): Show |
5 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1720-658G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712344 | |||||||
| chr20:43712376 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1720-626G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712376 | |||||||
| chr20:43712712 | G | A | 5 | a0004c0006t0002g0005 a0004c0006t0002g0101 a0004c0006t0002g0102 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720-290G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712712 | |||||||
| chr20:43712790 | A | C | 1 | a0002c0004t0001g0098 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1720-212A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712790 | |||||||
| chr20:43712924 | A | G | 23 | a0002c0003t0001g0217 a0002c0004t0001g0041 a0002c0004t0001g0042 others(20): Show |
23 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.1720-78A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 11/13 | chr20 | 43712924 | |||||||
| chr20:43713260 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1824+154G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713260 | |||||||
| chr20:43713309 | C | T | 5 | a0001c0002t0001g0092 a0002c0003t0001g0014 a0002c0003t0001g0015 others(2): Show |
5 | HG02300.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1824+203C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713309 | |||||||
| chr20:43713310 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1824+204G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713310 | |||||||
| chr20:43713312 | G | A | 6 | a0002c0007t0003g0106 a0002c0007t0003g0107 a0002c0007t0003g0108 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1824+206G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713312 | |||||||
| chr20:43713338 | A | G | 4 | a0001c0001t0001g0137 a0001c0001t0001g0150 a0001c0001t0001g0213 others(1): Show |
4 | NA18965.hp2 NA18990.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1824+232A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713338 | |||||||
| chr20:43713352 | C | T | 16 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(13): Show |
17 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1824+246C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713352 | |||||||
| chr20:43713391 | C | CT | 12 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(9): Show |
12 | HG01884.hp1 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1824+298dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43713391 | ||||||
| chr20:43713413 | A | G | 22 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(19): Show |
23 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1824+307A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713413 | |||||||
| chr20:43713421 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0172 a0001c0001t0001g0178 |
3 | HG01346.hp2 HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1824+315C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713421 | |||||||
| chr20:43713481 | G | A | 1 | a0003c0005t0001g0118 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1824+375G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713481 | |||||||
| chr20:43713549 | G | A | 6 | a0001c0017t0002g0124 a0004c0006t0002g0005 a0004c0006t0002g0101 others(3): Show |
7 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1824+443G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713549 | |||||||
| chr20:43713607 | G | A | 6 | a0002c0007t0003g0106 a0002c0007t0003g0107 a0002c0007t0003g0108 others(3): Show |
6 | HG01361.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1824+501G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713607 | |||||||
| chr20:43713676 | C | T | 26 | a0002c0003t0001g0217 a0002c0004t0001g0011 a0002c0004t0001g0012 others(23): Show |
26 | HG01081.hp1 HG01109.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.1824+570C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713676 | |||||||
| chr20:43713748 | T | G | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1824+642T>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713748 | |||||||
| chr20:43713780 | G | A | 1 | a0001c0002t0001g0064 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1824+674G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713780 | |||||||
| chr20:43713942 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1824+836T>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43713942 | |||||||
| chr20:43714036 | G | T | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1824+930G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714036 | |||||||
| chr20:43714081 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(218): Show |
230 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(227): Show |
intron_variant | MODIFIER | c.1824+975C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714081 | |||||||
| chr20:43714142 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1825-992A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714142 | |||||||
| chr20:43714281 | G | T | 15 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(12): Show |
15 | HG00741.hp2 HG01167.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1825-853G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714281 | |||||||
| chr20:43714387 | C | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(222): Show |
234 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(231): Show |
intron_variant | MODIFIER | c.1825-747C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714387 | |||||||
| chr20:43714421 | C | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1825-713C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714421 | |||||||
| chr20:43714471 | C | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(199): Show |
210 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.1825-663C>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714471 | |||||||
| chr20:43714495 | G | A | 7 | a0001c0001t0001g0204 a0001c0017t0002g0124 a0004c0006t0002g0005 others(4): Show |
8 | HG01243.hp1 HG02055.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825-639G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714495 | |||||||
| chr20:43714512 | A | G | 4 | a0001c0002t0001g0009 a0001c0002t0001g0010 a0001c0002t0001g0260 others(1): Show |
6 | HG01255.hp2 HG01496.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1825-622A>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714512 | |||||||
| chr20:43714581 | A | AT | 9 | a0001c0001t0001g0044 a0001c0001t0001g0088 a0001c0001t0001g0204 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825-541dupT | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr20 | 43714581 | ||||||
| chr20:43714730 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(199): Show |
210 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.1825-404G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714730 | |||||||
| chr20:43714793 | G | T | 1 | a0001c0002t0001g0235 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1825-341G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714793 | |||||||
| chr20:43714871 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1825-263C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714871 | |||||||
| chr20:43714957 | A | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0245 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1825-177A>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43714957 | |||||||
| chr20:43715045 | G | A | 5 | a0003c0005t0001g0117 a0003c0005t0001g0119 a0003c0005t0001g0120 others(2): Show |
5 | HG00741.hp2 HG01167.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825-89G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43715045 | |||||||
| chr20:43715067 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1825-67G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 12/13 | chr20 | 43715067 | |||||||
| chr20:43715376 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1974+93C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715376 | |||||||
| chr20:43715489 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1974+206T>C | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715489 | |||||||
| chr20:43715507 | C | G | 1 | a0002c0004t0001g0011 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1974+224C>G | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715507 | |||||||
| chr20:43715724 | G | A | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1975-235G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715724 | |||||||
| chr20:43715754 | G | T | 1 | a0003c0005t0001g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1975-205G>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715754 | |||||||
| chr20:43715791 | C | T | 4 | a0002c0003t0001g0014 a0002c0003t0001g0015 a0002c0003t0001g0016 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975-168C>T | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715791 | |||||||
| chr20:43715865 | G | A | 4 | a0002c0007t0003g0107 a0002c0007t0003g0108 a0002c0007t0003g0109 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1975-94G>A | MYBL2 | ENSG00000101057.16 | transcript | ENST00000217026.5 | protein_coding | 13/13 | chr20 | 43715865 |