Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23077 |
|---|---|
| ensemblid | ENSG00000005810.20 |
| hgncid | 23386 |
| symbol | MYCBP2 |
| name | MYC binding protein 2 |
| refseq_nuc | NM_015057.5 |
| refseq_prot | NP_055872.4 |
| ensembl_nuc | ENST00000544440.7 |
| ensembl_prot | ENSP00000444596.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 77044657 |
| end | 77327094 |
| strand | - |
| ver | v1.2 |
| region | chr13:77044657-77327094 |
| region5000 | chr13:77039657-77332094 |
| regionname0 | MYCBP2_chr13_77044657_77327094 |
| regionname5000 | MYCBP2_chr13_77039657_77332094 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 4678 | 304 | 69 | 54 | 145 | 8 | 26 | 108 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0002 | 0/0 | 4678 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0003 | 0/0 | 4678 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0004 | 0/0 | 4678 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0005 | 0/0 | 4678 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0006 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0007 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0008 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0009 | 0/0 | 4678 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0010 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0011 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0012 | 0/0 | 4678 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0013 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0014 | 0/0 | 4678 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0015 | 0/0 | 4678 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0016 | 0/0 | 4678 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0017 | 0/0 | 4678 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0018 | 0/0 | 4678 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 14037 | 114 | 14 | 25 | 58 | 3 | 14 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0002 | 0/1 | 14037 | 59 | 1 | 2 | 42 | 2 | 11 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0003 | 1/0 | 14037 | 38 | 30 | 7 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0004 | 0/0 | 14037 | 22 | 5 | 5 | 11 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0005 | 0/0 | 14037 | 19 | 0 | 1 | 17 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0006 | 0/0 | 14037 | 15 | 6 | 8 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0007 | 0/0 | 14037 | 8 | 7 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0008 | 0/0 | 14037 | 8 | 7 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0009 | 0/0 | 14037 | 7 | 0 | 0 | 7 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0010 | 0/0 | 14037 | 3 | 0 | 0 | 3 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0011 | 0/0 | 14037 | 3 | 0 | 0 | 3 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0012 | 0/0 | 14037 | 2 | 0 | 2 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0013 | 0/0 | 14037 | 2 | 0 | 0 | 2 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0014 | 0/0 | 14037 | 2 | 0 | 0 | 2 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0015 | 0/0 | 14037 | 2 | 0 | 0 | 2 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0016 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0017 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0018 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0019 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0020 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0021 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0022 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0023 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0024 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0025 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0026 | 0/0 | 14037 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0027 | 0/0 | 14037 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0028 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0029 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0030 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0031 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0032 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0033 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0034 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0035 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0036 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0037 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0038 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0039 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0040 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0041 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0042 | 0/0 | 14037 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0043 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0044 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| c0045 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1041 | 303 | 79 | 55 | 134 | 7 | 26 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| t0002 | 0/0 | 1040 | 22 | 0 | 2 | 18 | 1 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| t0003 | 0/0 | 1041 | 4 | 0 | 0 | 4 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| t0004 | 0/0 | 1041 | 2 | 0 | 0 | 2 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| t0005 | 0/0 | 1041 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| t0006 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| t0007 | 0/0 | 1041 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 14037 | 114 | 14 | 25 | 58 | 3 | 14 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0002 | 0/1 | 14037 | 59 | 1 | 2 | 42 | 2 | 11 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0003 | 1/0 | 14037 | 38 | 30 | 7 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0004 | 0/0 | 14037 | 22 | 5 | 5 | 11 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0005 | 0/0 | 14037 | 19 | 0 | 1 | 17 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0006 | 0/0 | 14037 | 15 | 6 | 8 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0008 | 0/0 | 14037 | 8 | 7 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0009 | 0/0 | 14037 | 7 | 0 | 0 | 7 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0012 | 0/0 | 14037 | 2 | 0 | 2 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0013 | 0/0 | 14037 | 2 | 0 | 0 | 2 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0014 | 0/0 | 14037 | 2 | 0 | 0 | 2 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0016 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0019 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0020 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0021 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0023 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0026 | 0/0 | 14037 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0029 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0030 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0031 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0033 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0034 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0035 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0036 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0043 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0044 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0045 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0002c0007 | 0/0 | 14037 | 8 | 7 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0002c0040 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0003c0010 | 0/0 | 14037 | 3 | 0 | 0 | 3 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0004c0011 | 0/0 | 14037 | 3 | 0 | 0 | 3 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0005c0015 | 0/0 | 14037 | 2 | 0 | 0 | 2 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0006c0017 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0007c0018 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0008c0039 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0009c0022 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0010c0025 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0011c0024 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0012c0038 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0013c0037 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0014c0032 | 0/0 | 14037 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0015c0027 | 0/0 | 14037 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0016c0028 | 0/0 | 14037 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0017c0041 | 0/0 | 14037 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0018c0042 | 0/0 | 14037 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 15077 | 109 | 14 | 25 | 53 | 3 | 14 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0001t0003 | 0/0 | 15077 | 3 | 0 | 0 | 3 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0001t0004 | 0/0 | 15077 | 2 | 0 | 0 | 2 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0002t0001 | 0/1 | 15077 | 58 | 1 | 2 | 42 | 2 | 10 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0002t0002 | 0/0 | 15076 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0003t0001 | 1/0 | 15077 | 37 | 29 | 7 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0003t0006 | 0/0 | 15077 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0004t0001 | 0/0 | 15077 | 22 | 5 | 5 | 11 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0005t0002 | 0/0 | 15076 | 19 | 0 | 1 | 17 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0006t0001 | 0/0 | 15077 | 15 | 6 | 8 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0008t0001 | 0/0 | 15077 | 8 | 7 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0009t0001 | 0/0 | 15077 | 7 | 0 | 0 | 7 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0012t0001 | 0/0 | 15077 | 2 | 0 | 2 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0013t0001 | 0/0 | 15077 | 2 | 0 | 0 | 2 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0014t0001 | 0/0 | 15077 | 2 | 0 | 0 | 2 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0016t0001 | 0/0 | 15077 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0019t0001 | 0/0 | 15077 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0020t0001 | 0/0 | 15077 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0021t0001 | 0/0 | 15077 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0023t0001 | 0/0 | 15077 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0026t0001 | 0/0 | 15077 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0029t0001 | 0/0 | 15077 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0030t0001 | 0/0 | 15077 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0031t0001 | 0/0 | 15077 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0033t0001 | 0/0 | 15077 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0034t0001 | 0/0 | 15077 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0035t0001 | 0/0 | 15077 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0036t0001 | 0/0 | 15077 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0043t0001 | 0/0 | 15077 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0044t0001 | 0/0 | 15077 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0001c0045t0001 | 0/0 | 15077 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0002c0007t0001 | 0/0 | 15077 | 8 | 7 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0002c0040t0001 | 0/0 | 15077 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0003c0010t0001 | 0/0 | 15077 | 3 | 0 | 0 | 3 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0004c0011t0001 | 0/0 | 15077 | 3 | 0 | 0 | 3 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0005c0015t0001 | 0/0 | 15077 | 2 | 0 | 0 | 2 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0006c0017t0001 | 0/0 | 15077 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0007c0018t0003 | 0/0 | 15077 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0008c0039t0001 | 0/0 | 15077 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0009c0022t0005 | 0/0 | 15077 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0010c0025t0001 | 0/0 | 15077 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0011c0024t0001 | 0/0 | 15077 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0012c0038t0002 | 0/0 | 15076 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0013c0037t0002 | 0/0 | 15076 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0014c0032t0001 | 0/0 | 15077 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0015c0027t0007 | 0/0 | 15077 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0016c0028t0001 | 0/0 | 15077 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0017c0041t0001 | 0/0 | 15077 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| a0018c0042t0001 | 0/0 | 15077 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | copy fasta | chr13 | 77039657 | 77332094 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0003t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0004t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0005t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0006t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0008t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0008t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0008t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0008t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0008t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0008t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0008t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0008t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0009t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0009t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0009t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0009t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0009t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0009t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0009t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0012t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0012t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0013t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0013t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0014t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0014t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0016t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0019t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0020t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0021t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0023t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0026t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0029t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0030t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0031t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0033t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0034t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0035t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0036t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0043t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0044t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0001c0045t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0002c0007t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0002c0007t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0002c0007t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0002c0007t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0002c0007t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0002c0007t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0002c0007t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0002c0007t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0002c0040t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0003c0010t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0003c0010t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0003c0010t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0004c0011t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0004c0011t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0004c0011t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0005c0015t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0005c0015t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0006c0017t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0007c0018t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0008c0039t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0009c0022t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0010c0025t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0011c0024t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0012c0038t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0013c0037t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0014c0032t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0015c0027t0007g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0016c0028t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0017c0041t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| a0018c0042t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0002 | g0138 | EUR | GBR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0157 | EUR | GBR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0036 | EUR | FIN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0294 | EUR | FIN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00408 | hp2 | a0001 | c0004 | t0001 | g0154 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0155 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00621 | hp1 | a0001 | c0009 | t0001 | g0076 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00621 | hp2 | a0001 | c0004 | t0001 | g0244 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00642 | hp1 | a0009 | c0022 | t0005 | g0185 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00642 | hp2 | a0001 | c0006 | t0001 | g0317 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00733 | hp1 | a0001 | c0004 | t0001 | g0277 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00733 | hp2 | a0001 | c0006 | t0001 | g0325 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00735 | hp1 | a0002 | c0007 | t0001 | g0218 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00735 | hp2 | a0001 | c0008 | t0001 | g0306 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00738 | hp2 | a0001 | c0006 | t0001 | g0324 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0210 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01069 | hp1 | a0001 | c0006 | t0001 | g0318 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01069 | hp2 | a0001 | c0012 | t0001 | g0075 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01071 | hp1 | a0001 | c0012 | t0001 | g0074 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0265 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01099 | hp1 | a0001 | c0016 | t0001 | g0006 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01167 | hp2 | a0001 | c0006 | t0001 | g0331 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01168 | hp1 | a0001 | c0006 | t0001 | g0321 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01169 | hp2 | a0001 | c0006 | t0001 | g0330 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0035 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01256 | hp1 | a0001 | c0006 | t0001 | g0323 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0260 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0261 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0267 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0098 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01496 | hp2 | a0012 | c0038 | t0002 | g0198 | AMR | CLM | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | IBS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0069 | EUR | IBS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01516 | hp1 | a0001 | c0006 | t0001 | g0326 | EUR | IBS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01891 | hp2 | a0001 | c0006 | t0001 | g0320 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01928 | hp1 | a0001 | c0005 | t0002 | g0273 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01952 | hp1 | a0001 | c0004 | t0001 | g0303 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01978 | hp1 | a0016 | c0028 | t0001 | g0241 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG01981 | hp2 | a0001 | c0030 | t0001 | g0037 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0289 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02055 | hp1 | a0001 | c0036 | t0001 | g0291 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0266 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02071 | hp1 | a0001 | c0029 | t0001 | g0065 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02080 | hp1 | a0001 | c0043 | t0001 | g0292 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02132 | hp1 | a0001 | c0009 | t0001 | g0220 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02132 | hp2 | a0001 | c0005 | t0002 | g0221 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0031 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | CDX | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02155 | hp2 | a0001 | c0019 | t0001 | g0274 | EAS | CDX | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | CDX | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0174 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02273 | hp2 | a0001 | c0004 | t0001 | g0293 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02293 | hp2 | a0001 | c0044 | t0001 | g0332 | AMR | PEL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02451 | hp1 | a0002 | c0007 | t0001 | g0213 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0088 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02523 | hp1 | a0011 | c0024 | t0001 | g0092 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02523 | hp2 | a0001 | c0009 | t0001 | g0077 | EAS | KHV | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0042 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0129 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02622 | hp1 | a0001 | c0034 | t0001 | g0024 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0287 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02647 | hp1 | a0001 | c0045 | t0001 | g0327 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0264 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02818 | hp2 | a0001 | c0008 | t0001 | g0309 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0029 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0207 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02895 | hp2 | a0001 | c0006 | t0001 | g0328 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0096 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02896 | hp2 | a0002 | c0007 | t0001 | g0214 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02897 | hp1 | a0001 | c0006 | t0001 | g0329 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02897 | hp2 | a0002 | c0007 | t0001 | g0216 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02922 | hp1 | a0006 | c0017 | t0001 | g0126 | AFR | ESN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02922 | hp2 | a0001 | c0008 | t0001 | g0263 | AFR | ESN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02970 | hp1 | a0010 | c0025 | t0001 | g0086 | AFR | ESN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0295 | AFR | ESN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02976 | hp2 | a0001 | c0006 | t0001 | g0333 | AFR | ESN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0072 | AFR | GWD | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0019 | AFR | ESN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03130 | hp2 | a0001 | c0035 | t0001 | g0030 | AFR | ESN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03139 | hp1 | a0001 | c0008 | t0001 | g0302 | AFR | ESN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0151 | AFR | ESN | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03209 | hp1 | a0002 | c0007 | t0001 | g0215 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0097 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0071 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03225 | hp2 | a0001 | c0021 | t0001 | g0301 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03453 | hp1 | a0002 | c0007 | t0001 | g0212 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03453 | hp2 | a0001 | c0008 | t0001 | g0305 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | STU | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03704 | hp1 | a0018 | c0042 | t0001 | g0109 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03704 | hp2 | a0015 | c0027 | t0007 | g0180 | SAS | PJL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | BEB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0053 | SAS | STU | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | BEB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0114 | SAS | STU | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0199 | SAS | STU | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18522 | hp1 | a0001 | c0003 | t0006 | g0209 | AFR | YRI | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18522 | hp2 | a0001 | c0006 | t0001 | g0319 | AFR | YRI | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18612 | hp1 | a0001 | c0009 | t0001 | g0310 | EAS | CHB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | CHB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | CHB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18906 | hp1 | a0002 | c0007 | t0001 | g0219 | AFR | YRI | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | YRI | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18942 | hp1 | a0007 | c0018 | t0003 | g0004 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18943 | hp2 | a0003 | c0010 | t0001 | g0111 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18945 | hp1 | a0003 | c0010 | t0001 | g0112 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18946 | hp1 | a0001 | c0005 | t0002 | g0132 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18946 | hp2 | a0001 | c0004 | t0001 | g0153 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18947 | hp2 | a0001 | c0004 | t0001 | g0243 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18950 | hp1 | a0001 | c0014 | t0001 | g0050 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18950 | hp2 | a0004 | c0011 | t0001 | g0148 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18952 | hp1 | a0001 | c0005 | t0002 | g0222 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18960 | hp2 | a0008 | c0039 | t0001 | g0118 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18961 | hp1 | a0017 | c0041 | t0001 | g0084 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18964 | hp1 | a0001 | c0004 | t0001 | g0278 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18966 | hp2 | a0001 | c0005 | t0002 | g0137 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18968 | hp1 | a0001 | c0013 | t0001 | g0191 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18971 | hp1 | a0001 | c0020 | t0001 | g0147 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18972 | hp1 | a0003 | c0010 | t0001 | g0106 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18972 | hp2 | a0001 | c0004 | t0001 | g0240 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18977 | hp1 | a0013 | c0037 | t0002 | g0134 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18978 | hp2 | a0001 | c0005 | t0002 | g0133 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18979 | hp1 | a0001 | c0013 | t0001 | g0192 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18981 | hp1 | a0001 | c0005 | t0002 | g0272 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18982 | hp1 | a0001 | c0005 | t0002 | g0268 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18983 | hp1 | a0001 | c0005 | t0002 | g0269 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18984 | hp2 | a0001 | c0004 | t0001 | g0087 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18989 | hp2 | a0001 | c0005 | t0002 | g0135 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18994 | hp1 | a0004 | c0011 | t0001 | g0152 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18995 | hp1 | a0001 | c0004 | t0001 | g0150 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18995 | hp2 | a0001 | c0005 | t0002 | g0223 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18998 | hp2 | a0001 | c0005 | t0002 | g0136 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19002 | hp1 | a0001 | c0005 | t0002 | g0131 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19010 | hp1 | a0001 | c0014 | t0001 | g0051 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19010 | hp2 | a0001 | c0005 | t0002 | g0078 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19012 | hp1 | a0005 | c0015 | t0001 | g0113 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | LWK | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | LWK | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19054 | hp2 | a0001 | c0023 | t0001 | g0206 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19056 | hp2 | a0001 | c0005 | t0002 | g0270 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19058 | hp1 | a0001 | c0005 | t0002 | g0224 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19060 | hp1 | a0001 | c0005 | t0002 | g0079 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19060 | hp2 | a0005 | c0015 | t0001 | g0258 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19064 | hp2 | a0004 | c0011 | t0001 | g0156 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0279 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19066 | hp1 | a0001 | c0031 | t0001 | g0070 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19068 | hp1 | a0001 | c0009 | t0001 | g0311 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19074 | hp2 | a0001 | c0004 | t0001 | g0242 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19079 | hp1 | a0001 | c0005 | t0002 | g0271 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19085 | hp2 | a0001 | c0009 | t0001 | g0127 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19090 | hp1 | a0001 | c0009 | t0001 | g0128 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | YRI | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA20129 | hp1 | a0002 | c0040 | t0001 | g0297 | AFR | ASW | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA20129 | hp2 | a0001 | c0006 | t0001 | g0322 | AFR | ASW | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA20905 | hp2 | a0001 | c0026 | t0001 | g0285 | SAS | GIH | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02109 | hp1 | a0014 | c0032 | t0001 | g0038 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02109 | hp2 | a0001 | c0008 | t0001 | g0296 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02486 | hp2 | a0002 | c0007 | t0001 | g0217 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | ACB | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03471 | hp1 | a0001 | c0033 | t0001 | g0045 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG03471 | hp2 | a0001 | c0008 | t0001 | g0307 | AFR | MSL | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0028 | AFR | USA | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | USA | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| NA21309 | hp2 | a0001 | c0008 | t0001 | g0308 | AFR | LWK | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0201 | REF | REF | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0208 | REF | REF | MYCBP2_chr13_77039657_77332094 | MYCBP2 | chr13 | 77039657 | 77332094 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77044658
|
A | G | 1 | a0009 | 1 | HG00642.hp1 | splice_region_variant | LOW | c.*720T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 83/83 | chr13 | 77044658 | ||||||
| chr13:77077210
|
C | T | 1 | a0010 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.11662G>A | p.Val3888Met | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 67/83 | 11981/15077 | 11662/14037 | 3888/4678 | chr13 | 77077210 | ||
| chr13:77077365
|
A | G | 1 | a0011 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.11507T>C | p.Ile3836Thr | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 67/83 | 11826/15077 | 11507/14037 | 3836/4678 | chr13 | 77077365 | ||
| chr13:77098632
|
C | T | 1 | a0009 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.8522G>A | p.Arg2841His | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/83 | 8841/15077 | 8522/14037 | 2841/4678 | chr13 | 77098632 | ||
| chr13:77098978
|
C | T | 1 | a0003 | 3 | NA18943.hp2 NA18945.hp1 NA18972.hp1 |
missense_variant | MODERATE | c.8176G>A | p.Ala2726Thr | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/83 | 8495/15077 | 8176/14037 | 2726/4678 | chr13 | 77098978 | ||
| chr13:77125461
|
T | C | 1 | a0012 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.7892A>G | p.Asn2631Ser | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/83 | 8211/15077 | 7892/14037 | 2631/4678 | chr13 | 77125461 | ||
| chr13:77126535
|
T | C | 1 | a0013 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.7667A>G | p.Lys2556Arg | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 53/83 | 7986/15077 | 7667/14037 | 2556/4678 | chr13 | 77126535 | ||
| chr13:77158027
|
T | C | 1 | a0014 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.6680A>G | p.Asn2227Ser | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/83 | 6999/15077 | 6680/14037 | 2227/4678 | chr13 | 77158027 | ||
| chr13:77164510
|
T | C | 1 | a0015 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.6491A>G | p.Asn2164Ser | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/83 | 6810/15077 | 6491/14037 | 2164/4678 | chr13 | 77164510 | ||
| chr13:77166442
|
T | C | 1 | a0016 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.6227A>G | p.Asn2076Ser | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 41/83 | 6546/15077 | 6227/14037 | 2076/4678 | chr13 | 77166442 | ||
| chr13:77166443
|
T | C | 1 | a0008 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.6226A>G | p.Asn2076Asp | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 41/83 | 6545/15077 | 6226/14037 | 2076/4678 | chr13 | 77166443 | ||
| chr13:77171531
|
C | A | 1 | a0002 | 9 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
missense_variant | MODERATE | c.5755G>T | p.Ala1919Ser | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/83 | 6074/15077 | 5755/14037 | 1919/4678 | chr13 | 77171531 | ||
| chr13:77185330
|
T | C | 1 | a0004 | 3 | NA18950.hp2 NA18994.hp1 NA19064.hp2 |
missense_variant | MODERATE | c.4492A>G | p.Ile1498Val | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/83 | 4811/15077 | 4492/14037 | 1498/4678 | chr13 | 77185330 | ||
| chr13:77224511
|
T | C | 1 | a0017 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.2879A>G | p.Asp960Gly | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/83 | 3198/15077 | 2879/14037 | 960/4678 | chr13 | 77224511 | ||
| chr13:77251194
|
C | A | 1 | a0018 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.2338G>T | p.Ala780Ser | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/83 | 2657/15077 | 2338/14037 | 780/4678 | chr13 | 77251194 | ||
| chr13:77261297
|
T | C | 1 | a0005 | 2 | NA19012.hp1 NA19060.hp2 |
missense_variant | MODERATE | c.1726A>G | p.Ile576Val | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 12/83 | 2045/15077 | 1726/14037 | 576/4678 | chr13 | 77261297 | ||
| chr13:77262087
|
C | T | 1 | a0007 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.1613G>A | p.Arg538Gln | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 11/83 | 1932/15077 | 1613/14037 | 538/4678 | chr13 | 77262087 | ||
| chr13:77278859
|
A | C | 1 | a0006 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.647T>G | p.Phe216Cys | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/83 | 966/15077 | 647/14037 | 216/4678 | chr13 | 77278859 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77045402
|
C | T | 1 | a0002c0007 | 8 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
synonymous_variant | LOW | c.14013G>A | p.Val4671Val | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 83/83 | 14332/15077 | 14013/14037 | 4671/4678 | chr13 | 77045402 | ||
| chr13:77051811
|
C | T | 1 | a0001c0026 | 1 | NA20905.hp2 | splice_region_variant&synonymous_variant | LOW | c.13755G>A | p.Gln4585Gln | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 81/83 | 14074/15077 | 13755/14037 | 4585/4678 | chr13 | 77051811 | ||
| chr13:77058335
|
C | T | 5 | a0001c0004a0001c0020a0001c0043others(2): Show | 28 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(25): Show |
synonymous_variant | LOW | c.13212G>A | p.Glu4404Glu | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/83 | 13531/15077 | 13212/14037 | 4404/4678 | chr13 | 77058335 | ||
| chr13:77077154
|
C | T | 1 | a0001c0008 | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
synonymous_variant | LOW | c.11718G>A | p.Thr3906Thr | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 67/83 | 12037/15077 | 11718/14037 | 3906/4678 | chr13 | 77077154 | ||
| chr13:77078827
|
C | T | 1 | a0001c0036 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.11481G>A | p.Lys3827Lys | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 66/83 | 11800/15077 | 11481/14037 | 3827/4678 | chr13 | 77078827 | ||
| chr13:77081894
|
G | T | 1 | a0001c0035 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.11136C>A | p.Gly3712Gly | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 64/83 | 11455/15077 | 11136/14037 | 3712/4678 | chr13 | 77081894 | ||
| chr13:77083130
|
A | T | 1 | a0001c0023 | 1 | NA19054.hp2 | synonymous_variant | LOW | c.10938T>A | p.Ala3646Ala | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/83 | 11257/15077 | 10938/14037 | 3646/4678 | chr13 | 77083130 | ||
| chr13:77089003
|
C | T | 3 | a0001c0005a0012c0038a0013c0037 | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
synonymous_variant | LOW | c.10554G>A | p.Pro3518Pro | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 61/83 | 10873/15077 | 10554/14037 | 3518/4678 | chr13 | 77089003 | ||
| chr13:77097440
|
A | G | 1 | a0001c0034 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.9714T>C | p.Asp3238Asp | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/83 | 10033/15077 | 9714/14037 | 3238/4678 | chr13 | 77097440 | ||
| chr13:77097458
|
T | A | 1 | a0001c0031 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.9696A>T | p.Val3232Val | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/83 | 10015/15077 | 9696/14037 | 3232/4678 | chr13 | 77097458 | ||
| chr13:77140134
|
C | T | 1 | a0001c0013 | 2 | NA18968.hp1 NA18979.hp1 |
synonymous_variant | LOW | c.7431G>A | p.Ala2477Ala | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 51/83 | 7750/15077 | 7431/14037 | 2477/4678 | chr13 | 77140134 | ||
| chr13:77140137
|
A | G | 1 | a0001c0030 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.7428T>C | p.Ser2476Ser | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 51/83 | 7747/15077 | 7428/14037 | 2476/4678 | chr13 | 77140137 | ||
| chr13:77158073
|
G | A | 1 | a0012c0038 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.6634C>T | p.Leu2212Leu | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/83 | 6953/15077 | 6634/14037 | 2212/4678 | chr13 | 77158073 | ||
| chr13:77161924
|
A | G | 1 | a0001c0033 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.6579T>C | p.Leu2193Leu | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/83 | 6898/15077 | 6579/14037 | 2193/4678 | chr13 | 77161924 | ||
| chr13:77161933
|
A | C | 1 | a0001c0029 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.6570T>G | p.Leu2190Leu | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/83 | 6889/15077 | 6570/14037 | 2190/4678 | chr13 | 77161933 | ||
| chr13:77164529
|
A | G | 13 | a0001c0002a0001c0006a0001c0014others(10): Show | 89 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
synonymous_variant | LOW | c.6472T>C | p.Leu2158Leu | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/83 | 6791/15077 | 6472/14037 | 2158/4678 | chr13 | 77164529 | ||
| chr13:77166522
|
T | G | 1 | a0001c0044 | 1 | HG02293.hp2 | synonymous_variant | LOW | c.6147A>C | p.Thr2049Thr | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 41/83 | 6466/15077 | 6147/14037 | 2049/4678 | chr13 | 77166522 | ||
| chr13:77171538
|
G | C | 1 | a0001c0008 | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
synonymous_variant | LOW | c.5748C>G | p.Val1916Val | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/83 | 6067/15077 | 5748/14037 | 1916/4678 | chr13 | 77171538 | ||
| chr13:77177757
|
C | T | 17 | a0001c0001a0001c0004a0001c0009others(14): Show | 160 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(157): Show |
synonymous_variant | LOW | c.5331G>A | p.Leu1777Leu | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/83 | 5650/15077 | 5331/14037 | 1777/4678 | chr13 | 77177757 | ||
| chr13:77180145
|
C | G | 1 | a0001c0021 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.5115G>C | p.Ala1705Ala | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/83 | 5434/15077 | 5115/14037 | 1705/4678 | chr13 | 77180145 | ||
| chr13:77194206
|
A | G | 1 | a0001c0020 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.3882T>C | p.Thr1294Thr | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/83 | 4201/15077 | 3882/14037 | 1294/4678 | chr13 | 77194206 | ||
| chr13:77212125
|
T | C | 1 | a0001c0014 | 2 | NA18950.hp1 NA19010.hp1 |
synonymous_variant | LOW | c.3093A>G | p.Pro1031Pro | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 22/83 | 3412/15077 | 3093/14037 | 1031/4678 | chr13 | 77212125 | ||
| chr13:77217906
|
A | C | 1 | a0001c0019 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.2991T>G | p.Thr997Thr | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/83 | 3310/15077 | 2991/14037 | 997/4678 | chr13 | 77217906 | ||
| chr13:77243933
|
G | A | 1 | a0001c0045 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.2400C>T | p.Ser800Ser | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 16/83 | 2719/15077 | 2400/14037 | 800/4678 | chr13 | 77243933 | ||
| chr13:77260492
|
A | C | 2 | a0001c0009a0001c0012 | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
synonymous_variant | LOW | c.1953T>G | p.Ser651Ser | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/83 | 2272/15077 | 1953/14037 | 651/4678 | chr13 | 77260492 | ||
| chr13:77261256
|
G | A | 1 | a0001c0043 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1767C>T | p.His589His | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 12/83 | 2086/15077 | 1767/14037 | 589/4678 | chr13 | 77261256 | ||
| chr13:77326623
|
C | T | 1 | a0001c0016 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.153G>A | p.Leu51Leu | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/83 | 472/15077 | 153/14037 | 51/4678 | chr13 | 77326623 | ||
| chr13:77326713
|
T | A | 3 | a0001c0006a0001c0044a0001c0045 | 17 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(14): Show |
synonymous_variant | LOW | c.63A>T | p.Gly21Gly | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/83 | 382/15077 | 63/14037 | 21/4678 | chr13 | 77326713 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77044901
|
GT | G | 4 | a0001c0002t0002a0001c0005t0002a0012c0038t0002others(1): Show | 22 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*476delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 83/83 | 476 | chr13 | 77044901 | |||||
| chr13:77044915
|
T | A | 1 | a0001c0003t0006 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*463A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 83/83 | 463 | chr13 | 77044915 | |||||
| chr13:77045048
|
C | T | 1 | a0001c0001t0004 | 2 | NA18942.hp2 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*330G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 83/83 | 330 | chr13 | 77045048 | |||||
| chr13:77045336
|
T | C | 1 | a0015c0027t0007 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 83/83 | 42 | chr13 | 77045336 | |||||
| chr13:77045372
|
C | T | 2 | a0001c0001t0003a0007c0018t0003 | 4 | NA18942.hp1 NA18957.hp2 NA18982.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 83/83 | 6 | chr13 | 77045372 | |||||
| chr13:77327068
|
C | T | 2 | a0001c0001t0003a0007c0018t0003 | 4 | NA18942.hp1 NA18957.hp2 NA18982.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-293G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/83 | 293 | chr13 | 77327068 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77045662
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13922-169A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77045662 | ||||||
| chr13:77045757
|
C | T | 2 | a0001c0004t0001g0154a0001c0004t0001g0278 | 2 | HG00408.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.13922-264G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77045757 | ||||||
| chr13:77045847
|
T | G | 1 | a0001c0044t0001g0332 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.13922-354A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77045847 | ||||||
| chr13:77046180
|
G | T | 1 | a0001c0044t0001g0332 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.13922-687C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77046180 | ||||||
| chr13:77046417
|
C | A | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.13922-924G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77046417 | ||||||
| chr13:77046588
|
G | C | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.13922-1095C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77046588 | ||||||
| chr13:77046882
|
A | G | 34 | a0001c0003t0001g0129a0001c0003t0001g0207a0001c0003t0006g0209others(31): Show | 34 | HG00099.hp1 HG00621.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.13922-1389T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77046882 | ||||||
| chr13:77046925
|
C | G | 249 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.13922-1432G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77046925 | ||||||
| chr13:77046942
|
C | T | 2 | a0001c0002t0001g0001a0001c0002t0001g0114 | 3 | HG03490.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.13922-1449G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77046942 | ||||||
| chr13:77047045
|
A | G | 19 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(16): Show | 19 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.13922-1552T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77047045 | ||||||
| chr13:77047134
|
C | T | 50 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(47): Show | 50 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.13922-1641G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77047134 | ||||||
| chr13:77047309
|
CT | C | 3 | a0001c0002t0001g0026a0005c0015t0001g0113a0005c0015t0001g0258 | 3 | HG00544.hp2 NA19012.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.13922-1817delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77047309 | ||||||
| chr13:77047646
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.13922-2153C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77047646 | ||||||
| chr13:77047679
|
A | C | 1 | a0001c0004t0001g0155 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.13922-2186T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77047679 | ||||||
| chr13:77047704
|
A | C | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.13922-2211T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77047704 | ||||||
| chr13:77047815
|
G | A | 1 | a0001c0002t0001g0048 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.13922-2322C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77047815 | ||||||
| chr13:77047851
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.13922-2358G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77047851 | ||||||
| chr13:77047880
|
C | T | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.13922-2387G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77047880 | ||||||
| chr13:77047980
|
G | A | 1 | a0001c0002t0001g0204 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.13922-2487C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77047980 | ||||||
| chr13:77048556
|
G | A | 8 | a0001c0003t0001g0015a0001c0003t0001g0017a0001c0003t0001g0018others(5): Show | 8 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.13921+2441C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77048556 | ||||||
| chr13:77048681
|
C | T | 42 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(39): Show | 42 | HG00099.hp1 HG00621.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.13921+2316G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77048681 | ||||||
| chr13:77048683
|
C | T | 243 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.13921+2314G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77048683 | ||||||
| chr13:77048687
|
T | C | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.13921+2310A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77048687 | ||||||
| chr13:77048707
|
T | C | 1 | a0001c0008t0001g0307 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.13921+2290A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77048707 | ||||||
| chr13:77048861
|
T | TA | 43 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(40): Show | 43 | HG00099.hp1 HG00621.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.13921+2135dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77048861 | ||||||
| chr13:77049124
|
A | T | 1 | a0015c0027t0007g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.13921+1873T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049124 | ||||||
| chr13:77049192
|
C | A | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.13921+1805G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049192 | ||||||
| chr13:77049281
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.13921+1716G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049281 | ||||||
| chr13:77049330
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.13921+1667G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049330 | ||||||
| chr13:77049354
|
T | C | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.13921+1643A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049354 | ||||||
| chr13:77049403
|
A | T | 1 | a0001c0002t0001g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.13921+1594T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049403 | ||||||
| chr13:77049411
|
GTA | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.13921+1584_13921+1 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049411 | ||||||
| chr13:77049774
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.13921+1223A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049774 | ||||||
| chr13:77049790
|
C | T | 20 | a0001c0004t0001g0087a0001c0004t0001g0088a0001c0004t0001g0150others(17): Show | 20 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.13921+1207G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049790 | ||||||
| chr13:77049834
|
C | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0167a0001c0001t0001g0169others(14): Show | 17 | HG00544.hp1 HG02015.hp2 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.13921+1163G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049834 | ||||||
| chr13:77049856
|
G | A | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.13921+1141C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049856 | ||||||
| chr13:77049979
|
C | G | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.13921+1018G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77049979 | ||||||
| chr13:77050023
|
A | T | 242 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.13921+974T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050023 | ||||||
| chr13:77050112
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.13921+885G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050112 | ||||||
| chr13:77050207
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.13921+790G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050207 | ||||||
| chr13:77050254
|
G | A | 20 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(17): Show | 20 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.13921+743C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050254 | ||||||
| chr13:77050263
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.13921+734A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050263 | ||||||
| chr13:77050369
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.13921+628T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050369 | ||||||
| chr13:77050370
|
T | C | 36 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(33): Show | 36 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.13921+627A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050370 | ||||||
| chr13:77050413
|
G | A | 1 | a0001c0002t0001g0171 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.13921+584C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050413 | ||||||
| chr13:77050432
|
C | T | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.13921+565G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050432 | ||||||
| chr13:77050651
|
T | TA | 23 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(20): Show | 23 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.13921+345dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050651 | ||||||
| chr13:77050651
|
TA | T | 17 | a0001c0001t0001g0085a0001c0002t0001g0026a0001c0002t0001g0060others(14): Show | 17 | HG00544.hp2 HG00621.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.13921+345delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050651 | ||||||
| chr13:77050788
|
G | A | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.13921+209C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050788 | ||||||
| chr13:77050837
|
C | T | 108 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(105): Show | 108 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.13921+160G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050837 | ||||||
| chr13:77050883
|
T | C | 1 | a0001c0002t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.13921+114A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050883 | ||||||
| chr13:77050983
|
T | C | 1 | a0001c0003t0001g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.13921+14A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 82/82 | chr13 | 77050983 | ||||||
| chr13:77051226
|
T | C | 3 | a0001c0002t0001g0057a0001c0002t0001g0062a0001c0002t0001g0063 | 3 | HG00423.hp1 NA18981.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.13756-64A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 81/82 | chr13 | 77051226 | ||||||
| chr13:77051416
|
G | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.13756-254C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 81/82 | chr13 | 77051416 | ||||||
| chr13:77051526
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.13755+285T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 81/82 | chr13 | 77051526 | ||||||
| chr13:77051549
|
T | G | 20 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(17): Show | 20 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.13755+262A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 81/82 | chr13 | 77051549 | ||||||
| chr13:77051583
|
A | G | 1 | a0001c0002t0001g0099 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.13755+228T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 81/82 | chr13 | 77051583 | ||||||
| chr13:77051638
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.13755+173G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 81/82 | chr13 | 77051638 | ||||||
| chr13:77051665
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.13755+146A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 81/82 | chr13 | 77051665 | ||||||
| chr13:77052248
|
G | C | 1 | a0001c0002t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.13648-330C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77052248 | ||||||
| chr13:77052274
|
C | T | 1 | a0001c0003t0001g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.13648-356G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77052274 | ||||||
| chr13:77052275
|
G | A | 37 | a0001c0002t0001g0001a0001c0002t0001g0099a0001c0002t0001g0100others(34): Show | 38 | HG00597.hp2 HG00673.hp1 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.13648-357C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77052275 | ||||||
| chr13:77052344
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.13648-426C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77052344 | ||||||
| chr13:77052347
|
C | T | 6 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.13648-429G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77052347 | ||||||
| chr13:77052510
|
G | A | 6 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.13648-592C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77052510 | ||||||
| chr13:77052998
|
C | T | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.13648-1080G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77052998 | ||||||
| chr13:77053039
|
G | C | 1 | a0001c0002t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.13648-1121C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77053039 | ||||||
| chr13:77053071
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.13648-1153C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77053071 | ||||||
| chr13:77053409
|
T | G | 36 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(33): Show | 36 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.13648-1491A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77053409 | ||||||
| chr13:77053494
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.13648-1576G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77053494 | ||||||
| chr13:77053562
|
T | G | 1 | a0001c0004t0001g0153 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.13648-1644A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77053562 | ||||||
| chr13:77053653
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.13648-1735A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77053653 | ||||||
| chr13:77054077
|
T | C | 1 | a0001c0002t0001g0124 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.13647+1481A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054077 | ||||||
| chr13:77054141
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.13647+1417A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054141 | ||||||
| chr13:77054169
|
A | G | 8 | a0002c0007t0001g0212a0002c0007t0001g0213a0002c0007t0001g0214others(5): Show | 8 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.13647+1389T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054169 | ||||||
| chr13:77054247
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13647+1311A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054247 | ||||||
| chr13:77054403
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.13647+1155T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054403 | ||||||
| chr13:77054410
|
A | AT | 31 | a0001c0003t0001g0129a0001c0005t0002g0078a0001c0005t0002g0079others(28): Show | 31 | HG00099.hp1 HG00621.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.13647+1147dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054410 | ||||||
| chr13:77054419
|
A | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.13647+1139T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054419 | ||||||
| chr13:77054528
|
G | C | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.13647+1030C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054528 | ||||||
| chr13:77054529
|
A | T | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.13647+1029T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054529 | ||||||
| chr13:77054603
|
C | CT | 36 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(33): Show | 36 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.13647+954dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054603 | ||||||
| chr13:77054747
|
G | A | 107 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(104): Show | 107 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.13647+811C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054747 | ||||||
| chr13:77054969
|
C | T | 1 | a0001c0020t0001g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.13647+589G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77054969 | ||||||
| chr13:77055009
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.13647+549C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77055009 | ||||||
| chr13:77055011
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.13647+547C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77055011 | ||||||
| chr13:77055066
|
G | A | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.13647+492C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77055066 | ||||||
| chr13:77055069
|
A | C | 1 | a0001c0008t0001g0305 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13647+489T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77055069 | ||||||
| chr13:77055132
|
TA | T | 14 | a0001c0001t0001g0081a0001c0001t0001g0239a0001c0002t0001g0102others(11): Show | 14 | HG00735.hp2 HG01257.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.13647+425delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77055132 | ||||||
| chr13:77055143
|
AAAG | A | 71 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(68): Show | 71 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.13647+412_13647+41 others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77055143 | ||||||
| chr13:77055254
|
G | A | 1 | a0001c0002t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.13647+304C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77055254 | ||||||
| chr13:77055409
|
TGGAAACA others(3): Show |
T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.13647+139_13647+14 others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 80/82 | chr13 | 77055409 | ||||||
| chr13:77055795
|
C | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.13438-28G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77055795 | ||||||
| chr13:77055819
|
A | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.13438-52T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77055819 | ||||||
| chr13:77055842
|
G | A | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.13438-75C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77055842 | ||||||
| chr13:77055852
|
T | C | 15 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(12): Show | 15 | HG00735.hp1 HG01981.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.13438-85A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77055852 | ||||||
| chr13:77055915
|
T | C | 1 | a0002c0040t0001g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.13438-148A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77055915 | ||||||
| chr13:77056073
|
C | T | 5 | a0001c0006t0001g0317a0001c0006t0001g0318a0001c0006t0001g0330others(2): Show | 5 | HG00642.hp2 HG01069.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.13438-306G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056073 | ||||||
| chr13:77056098
|
T | TGG | 4 | a0001c0003t0001g0028a0001c0003t0001g0044a0001c0004t0001g0303others(1): Show | 4 | HG01952.hp1 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.13438-333_13438-33 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056098 | ||||||
| chr13:77056099
|
G | GGGGTGTG others(1): Show |
4 | a0001c0003t0001g0029a0001c0003t0001g0031a0001c0016t0001g0006others(1): Show | 4 | HG01099.hp1 HG02145.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.13438-333_13438-33 others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
G | GGT | 56 | a0001c0001t0001g0007a0001c0001t0001g0085a0001c0001t0001g0091others(53): Show | 56 | HG00408.hp2 HG00609.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.13438-334_13438-33 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
G | GGTGT | 27 | a0001c0001t0001g0082a0001c0001t0001g0094a0001c0001t0001g0140others(24): Show | 27 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.13438-336_13438-33 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
G | GGTGTGT | 37 | a0001c0001t0001g0013a0001c0001t0001g0083a0001c0001t0001g0093others(34): Show | 37 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.13438-338_13438-33 others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
G | GGTGTGTG others(1): Show |
24 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0167others(21): Show | 24 | HG00642.hp1 HG01167.hp1 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.13438-340_13438-33 others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
G | GGTGTGTG others(3): Show |
6 | a0001c0001t0001g0081a0001c0001t0001g0229a0001c0001t0001g0281others(3): Show | 6 | HG02293.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.13438-342_13438-33 others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
G | GGTGTGTG others(5): Show |
3 | a0001c0001t0001g0162a0001c0001t0001g0299a0001c0001t0001g0304 | 3 | HG00673.hp2 HG01106.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.13438-344_13438-33 others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
G | GGTGTGTG others(9): Show |
1 | a0001c0001t0001g0160 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.13438-348_13438-33 others(20): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
GGT | G | 38 | a0001c0001t0001g0130a0001c0001t0001g0145a0001c0001t0001g0158others(35): Show | 38 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.13438-334_13438-33 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
GGTGT | G | 22 | a0001c0001t0001g0176a0001c0001t0001g0232a0001c0001t0001g0238others(19): Show | 22 | HG00438.hp2 HG00621.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.13438-336_13438-33 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
GGTGTGT | G | 26 | a0001c0001t0001g0012a0001c0001t0001g0034a0001c0001t0001g0146others(23): Show | 26 | HG00099.hp2 HG00735.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.13438-338_13438-33 others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
GGTGTGTG others(1): Show |
G | 7 | a0001c0002t0001g0149a0001c0003t0001g0014a0001c0004t0001g0087others(4): Show | 7 | HG01496.hp2 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.13438-340_13438-33 others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
GGTGTGTG others(3): Show |
G | 4 | a0001c0001t0001g0009a0001c0002t0001g0099a0001c0006t0001g0319others(1): Show | 4 | HG02559.hp1 NA18522.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.13438-342_13438-33 others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
GGTGTGTG others(5): Show |
G | 1 | a0001c0003t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.13438-344_13438-33 others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
GGTGTGTG others(7): Show |
G | 3 | a0001c0001t0001g0233a0001c0002t0001g0104a0001c0004t0001g0088 | 3 | HG02451.hp2 HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.13438-346_13438-33 others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
GGTGTGTG others(9): Show |
G | 2 | a0001c0001t0001g0234a0001c0009t0001g0127 | 2 | NA19085.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.13438-348_13438-33 others(20): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
GGTGTGTG others(11): Show |
G | 1 | a0001c0004t0001g0243 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.13438-350_13438-33 others(22): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
GGTGTGTG others(13): Show |
G | 5 | a0001c0009t0001g0077a0001c0009t0001g0310a0001c0009t0001g0311others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.13438-352_13438-33 others(24): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056099
|
GGTGTGTG others(15): Show |
G | 3 | a0001c0009t0001g0076a0001c0009t0001g0128a0001c0009t0001g0220 | 3 | HG00621.hp1 HG02132.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.13438-354_13438-33 others(26): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056099 | ||||||
| chr13:77056101
|
T | G | 2 | a0001c0003t0001g0260a0001c0003t0001g0261 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.13438-334A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056101 | ||||||
| chr13:77056103
|
T | G | 3 | a0001c0003t0001g0046a0001c0003t0001g0096a0001c0033t0001g0045 | 3 | HG02818.hp1 HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.13438-336A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056103 | ||||||
| chr13:77056105
|
T | G | 1 | a0001c0003t0001g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.13438-338A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056105 | ||||||
| chr13:77056107
|
T | G | 3 | a0001c0003t0001g0033a0001c0003t0001g0035a0001c0035t0001g0030 | 3 | HG01243.hp1 HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.13438-340A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056107 | ||||||
| chr13:77056109
|
T | G | 1 | a0001c0003t0001g0014 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.13438-342A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056109 | ||||||
| chr13:77056158
|
GT | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0175a0002c0007t0001g0214 | 3 | HG01261.hp1 HG02602.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.13438-392delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056158 | ||||||
| chr13:77056159
|
T | TG | 3 | a0001c0001t0001g0290a0001c0002t0001g0062a0001c0005t0002g0133 | 3 | HG00544.hp1 NA18978.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.13438-393_13438-39 others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056159 | ||||||
| chr13:77056159
|
T | TGTGTGTG others(2): Show |
3 | a0001c0001t0004g0184a0001c0002t0001g0068a0001c0004t0001g0150 | 3 | HG02738.hp2 NA18966.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.13438-393_13438-39 others(13): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056159 | ||||||
| chr13:77056171
|
G | A | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.13438-404C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056171 | ||||||
| chr13:77056188
|
C | T | 3 | a0001c0001t0001g0168a0001c0001t0001g0182a0001c0001t0001g0248 | 3 | HG00609.hp1 HG02080.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.13438-421G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056188 | ||||||
| chr13:77056451
|
A | G | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.13437+535T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056451 | ||||||
| chr13:77056458
|
C | T | 1 | a0001c0003t0001g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.13437+528G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056458 | ||||||
| chr13:77056543
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.13437+443A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056543 | ||||||
| chr13:77056649
|
C | A | 2 | a0001c0003t0001g0015a0001c0003t0001g0017 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.13437+337G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056649 | ||||||
| chr13:77056803
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.13437+183A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056803 | ||||||
| chr13:77056859
|
T | G | 32 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(29): Show | 32 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.13437+127A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056859 | ||||||
| chr13:77056958
|
A | G | 2 | a0001c0003t0001g0022a0001c0003t0001g0023 | 2 | HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.13437+28T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 79/82 | chr13 | 77056958 | ||||||
| chr13:77057156
|
G | A | 2 | a0001c0009t0001g0077a0001c0009t0001g0127 | 2 | HG02523.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.13330-63C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77057156 | ||||||
| chr13:77057443
|
T | C | 11 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(8): Show | 11 | HG02717.hp2 HG02809.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.13330-350A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77057443 | ||||||
| chr13:77057472
|
A | C | 1 | a0001c0003t0001g0014 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.13330-379T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77057472 | ||||||
| chr13:77057813
|
A | AAAAAAGA others(4): Show |
9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.13329+394_13329+40 others(15): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77057813 | ||||||
| chr13:77057834
|
C | CT | 48 | a0001c0001t0001g0043a0001c0001t0001g0085a0001c0001t0001g0166others(45): Show | 48 | HG00423.hp1 HG00621.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.13329+383dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77057834 | ||||||
| chr13:77057834
|
CT | C | 7 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(4): Show | 7 | HG00408.hp1 HG01884.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.13329+383delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77057834 | ||||||
| chr13:77057834
|
CTTTTTTT | C | 33 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(30): Show | 33 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.13329+377_13329+38 others(11): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77057834 | ||||||
| chr13:77057907
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.13329+311T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77057907 | ||||||
| chr13:77057938
|
T | C | 13 | a0001c0003t0001g0129a0001c0003t0001g0207a0001c0003t0006g0209others(10): Show | 13 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.13329+280A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77057938 | ||||||
| chr13:77058086
|
T | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.13329+132A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77058086 | ||||||
| chr13:77058138
|
C | T | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.13329+80G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77058138 | ||||||
| chr13:77058196
|
A | G | 1 | a0009c0022t0005g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.13329+22T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 78/82 | chr13 | 77058196 | ||||||
| chr13:77058434
|
C | A | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.13141-28G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77058434 | ||||||
| chr13:77058589
|
G | A | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.13141-183C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77058589 | ||||||
| chr13:77058679
|
G | T | 1 | a0001c0002t0001g0259 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.13141-273C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77058679 | ||||||
| chr13:77058697
|
A | G | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.13141-291T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77058697 | ||||||
| chr13:77058854
|
G | A | 1 | a0014c0032t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.13141-448C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77058854 | ||||||
| chr13:77058902
|
T | C | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.13141-496A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77058902 | ||||||
| chr13:77058910
|
G | A | 152 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(149): Show | 152 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.13141-504C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77058910 | ||||||
| chr13:77058933
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.13141-527G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77058933 | ||||||
| chr13:77058934
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.13141-528C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77058934 | ||||||
| chr13:77058939
|
C | T | 6 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0164others(3): Show | 6 | HG01243.hp2 HG01261.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.13141-533G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77058939 | ||||||
| chr13:77058974
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.13140+549C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77058974 | ||||||
| chr13:77059046
|
T | C | 1 | a0001c0009t0001g0128 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.13140+477A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77059046 | ||||||
| chr13:77059057
|
C | T | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.13140+466G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77059057 | ||||||
| chr13:77059058
|
A | G | 52 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(49): Show | 52 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.13140+465T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77059058 | ||||||
| chr13:77059060
|
A | AT | 46 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(43): Show | 46 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(43): Show |
intron_variant | MODIFIER | c.13140+462dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77059060 | ||||||
| chr13:77059060
|
AT | A | 7 | a0001c0001t0001g0034a0001c0001t0001g0193a0001c0002t0001g0108others(4): Show | 7 | HG01069.hp1 HG01255.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.13140+462delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77059060 | ||||||
| chr13:77059074
|
T | TA | 4 | a0001c0002t0001g0056a0001c0002t0001g0057a0001c0002t0001g0062others(1): Show | 4 | HG00423.hp1 NA18978.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.13140+448dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77059074 | ||||||
| chr13:77059117
|
T | TAAGTG | 13 | a0001c0003t0001g0129a0001c0003t0001g0207a0001c0003t0006g0209others(10): Show | 13 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.13140+405_13140+40 others(9): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77059117 | ||||||
| chr13:77059354
|
C | T | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.13140+169G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77059354 | ||||||
| chr13:77059471
|
G | A | 1 | a0001c0002t0001g0119 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.13140+52C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77059471 | ||||||
| chr13:77059507
|
G | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.13140+16C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 77/82 | chr13 | 77059507 | ||||||
| chr13:77059826
|
C | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.13037-200G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 76/82 | chr13 | 77059826 | ||||||
| chr13:77059855
|
A | G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.13037-229T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 76/82 | chr13 | 77059855 | ||||||
| chr13:77060314
|
CA | C | 4 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(1): Show | 4 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.13037-689delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 76/82 | chr13 | 77060314 | ||||||
| chr13:77060364
|
C | T | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.13037-738G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 76/82 | chr13 | 77060364 | ||||||
| chr13:77060451
|
G | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.13036+718C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 76/82 | chr13 | 77060451 | ||||||
| chr13:77060858
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.13036+311T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 76/82 | chr13 | 77060858 | ||||||
| chr13:77061063
|
T | G | 1 | a0001c0002t0001g0036 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.13036+106A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 76/82 | chr13 | 77061063 | ||||||
| chr13:77061110
|
C | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.13036+59G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 76/82 | chr13 | 77061110 | ||||||
| chr13:77061392
|
G | A | 109 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(106): Show | 109 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.12904-91C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 75/82 | chr13 | 77061392 | ||||||
| chr13:77061586
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.12903+76A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 75/82 | chr13 | 77061586 | ||||||
| chr13:77061902
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.12775-112C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 74/82 | chr13 | 77061902 | ||||||
| chr13:77061933
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.12775-143A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 74/82 | chr13 | 77061933 | ||||||
| chr13:77062287
|
G | A | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.12774+309C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 74/82 | chr13 | 77062287 | ||||||
| chr13:77062325
|
A | G | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.12774+271T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 74/82 | chr13 | 77062325 | ||||||
| chr13:77062398
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.12774+198T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 74/82 | chr13 | 77062398 | ||||||
| chr13:77062420
|
T | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.12774+176A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 74/82 | chr13 | 77062420 | ||||||
| chr13:77063412
|
A | G | 1 | a0001c0003t0001g0210 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.12673-715T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 73/82 | chr13 | 77063412 | ||||||
| chr13:77063473
|
C | T | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.12673-776G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 73/82 | chr13 | 77063473 | ||||||
| chr13:77063513
|
G | A | 1 | a0001c0002t0001g0149 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.12673-816C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 73/82 | chr13 | 77063513 | ||||||
| chr13:77063558
|
CA | C | 272 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(269): Show | 273 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.12673-862delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 73/82 | chr13 | 77063558 | ||||||
| chr13:77063558
|
CAA | C | 30 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0161others(27): Show | 30 | HG00099.hp1 HG01168.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.12673-863_12673-86 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 73/82 | chr13 | 77063558 | ||||||
| chr13:77063582
|
G | C | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.12673-885C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 73/82 | chr13 | 77063582 | ||||||
| chr13:77063765
|
A | C | 1 | a0001c0001t0001g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.12672+850T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 73/82 | chr13 | 77063765 | ||||||
| chr13:77063785
|
C | T | 1 | a0001c0005t0002g0224 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.12672+830G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 73/82 | chr13 | 77063785 | ||||||
| chr13:77063964
|
T | G | 46 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(43): Show | 46 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(43): Show |
intron_variant | MODIFIER | c.12672+651A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 73/82 | chr13 | 77063964 | ||||||
| chr13:77064263
|
C | T | 1 | a0001c0009t0001g0128 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.12672+352G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 73/82 | chr13 | 77064263 | ||||||
| chr13:77064910
|
A | G | 2 | a0004c0011t0001g0148a0004c0011t0001g0152 | 2 | NA18950.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.12553-176T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 72/82 | chr13 | 77064910 | ||||||
| chr13:77065015
|
A | G | 2 | a0001c0003t0001g0018a0001c0003t0001g0019 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.12553-281T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 72/82 | chr13 | 77065015 | ||||||
| chr13:77065456
|
T | C | 72 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(69): Show | 72 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.12552+536A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 72/82 | chr13 | 77065456 | ||||||
| chr13:77065657
|
C | G | 2 | a0002c0007t0001g0214a0002c0007t0001g0216 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.12552+335G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 72/82 | chr13 | 77065657 | ||||||
| chr13:77065660
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.12552+332G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 72/82 | chr13 | 77065660 | ||||||
| chr13:77065664
|
C | T | 1 | a0001c0003t0001g0072 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.12552+328G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 72/82 | chr13 | 77065664 | ||||||
| chr13:77065890
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.12552+102T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 72/82 | chr13 | 77065890 | ||||||
| chr13:77066159
|
T | C | 1 | a0001c0001t0001g0238 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.12456-71A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77066159 | ||||||
| chr13:77066283
|
T | C | 1 | a0001c0003t0001g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.12456-195A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77066283 | ||||||
| chr13:77066397
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.12456-309C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77066397 | ||||||
| chr13:77066456
|
C | G | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.12456-368G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77066456 | ||||||
| chr13:77066457
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.12456-369A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77066457 | ||||||
| chr13:77066524
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.12456-436T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77066524 | ||||||
| chr13:77066677
|
T | C | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.12456-589A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77066677 | ||||||
| chr13:77066717
|
T | G | 2 | a0001c0003t0001g0015a0001c0003t0001g0017 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.12456-629A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77066717 | ||||||
| chr13:77066829
|
TTACTGGC others(28): Show |
T | 1 | a0001c0002t0001g0036 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.12455+717_12456-74 others(39): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77066829 | ||||||
| chr13:77067081
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.12455+500A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77067081 | ||||||
| chr13:77067114
|
T | C | 52 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(49): Show | 52 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.12455+467A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77067114 | ||||||
| chr13:77067332
|
G | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.12455+249C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77067332 | ||||||
| chr13:77067440
|
C | A | 3 | a0001c0001t0001g0280a0001c0003t0001g0207a0001c0003t0006g0209 | 3 | HG02258.hp2 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.12455+141G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 71/82 | chr13 | 77067440 | ||||||
| chr13:77068009
|
C | A | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.12172-145G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 70/82 | chr13 | 77068009 | ||||||
| chr13:77068077
|
G | A | 1 | a0001c0003t0001g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.12172-213C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 70/82 | chr13 | 77068077 | ||||||
| chr13:77068150
|
A | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.12172-286T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 70/82 | chr13 | 77068150 | ||||||
| chr13:77068223
|
G | C | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | NA18947.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.12171+342C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 70/82 | chr13 | 77068223 | ||||||
| chr13:77068243
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.12171+322A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 70/82 | chr13 | 77068243 | ||||||
| chr13:77068324
|
A | C | 2 | a0001c0003t0001g0020a0001c0003t0001g0021 | 2 | HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.12171+241T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 70/82 | chr13 | 77068324 | ||||||
| chr13:77068408
|
T | TAAAAAAA others(12): Show |
11 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(8): Show | 11 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.12171+156_12171+15 others(23): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 70/82 | chr13 | 77068408 | ||||||
| chr13:77068408
|
T | TAAAAAAA others(13): Show |
16 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(13): Show | 16 | HG02109.hp2 HG02717.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.12171+156_12171+15 others(24): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 70/82 | chr13 | 77068408 | ||||||
| chr13:77068408
|
T | TAAAAAAA others(14): Show |
23 | a0001c0003t0001g0031a0001c0005t0002g0078a0001c0005t0002g0079others(20): Show | 23 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.12171+156_12171+15 others(25): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 70/82 | chr13 | 77068408 | ||||||
| chr13:77068880
|
T | C | 1 | a0001c0031t0001g0070 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.11905-49A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77068880 | ||||||
| chr13:77068953
|
T | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.11905-122A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77068953 | ||||||
| chr13:77068973
|
CAT | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.11905-144_11905-14 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77068973 | ||||||
| chr13:77069016
|
A | G | 205 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.11905-185T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069016 | ||||||
| chr13:77069140
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.11905-309A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069140 | ||||||
| chr13:77069398
|
G | A | 4 | a0001c0001t0001g0085a0001c0003t0001g0207a0001c0003t0006g0209others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.11905-567C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069398 | ||||||
| chr13:77069407
|
G | C | 1 | a0001c0002t0001g0119 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.11905-576C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069407 | ||||||
| chr13:77069450
|
G | A | 1 | a0001c0002t0001g0259 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.11905-619C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069450 | ||||||
| chr13:77069505
|
C | T | 1 | a0001c0002t0001g0257 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.11905-674G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069505 | ||||||
| chr13:77069519
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.11905-688G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069519 | ||||||
| chr13:77069661
|
C | A | 2 | a0001c0012t0001g0074a0001c0012t0001g0075 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.11905-830G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069661 | ||||||
| chr13:77069689
|
T | C | 32 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(29): Show | 32 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.11905-858A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069689 | ||||||
| chr13:77069692
|
T | TA | 63 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0085others(60): Show | 63 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.11905-862dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069692 | ||||||
| chr13:77069817
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.11904+814C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069817 | ||||||
| chr13:77069884
|
A | T | 1 | a0001c0009t0001g0310 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.11904+747T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77069884 | ||||||
| chr13:77070251
|
C | T | 2 | a0001c0003t0001g0015a0001c0003t0001g0017 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.11904+380G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77070251 | ||||||
| chr13:77070334
|
C | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.11904+297G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77070334 | ||||||
| chr13:77070373
|
C | G | 1 | a0001c0003t0001g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.11904+258G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77070373 | ||||||
| chr13:77070402
|
G | C | 1 | a0001c0002t0001g0116 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.11904+229C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77070402 | ||||||
| chr13:77070573
|
A | AAC | 36 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0164others(33): Show | 36 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.11904+56_11904+57d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77070573 | ||||||
| chr13:77070573
|
A | AACAC | 6 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(3): Show | 6 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.11904+54_11904+57d others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 69/82 | chr13 | 77070573 | ||||||
| chr13:77070727
|
GA | G | 26 | a0001c0001t0001g0085a0001c0001t0001g0158a0001c0001t0001g0233others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.11824-17delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77070727 | ||||||
| chr13:77070922
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.11824-211T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77070922 | ||||||
| chr13:77071010
|
T | C | 1 | a0001c0003t0001g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.11824-299A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071010 | ||||||
| chr13:77071018
|
C | G | 1 | a0001c0002t0001g0025 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.11824-307G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071018 | ||||||
| chr13:77071112
|
TAAGCTAT others(22): Show |
T | 6 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.11824-430_11824-40 others(33): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071112 | ||||||
| chr13:77071200
|
C | T | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.11824-489G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071200 | ||||||
| chr13:77071237
|
G | GTA | 132 | a0001c0001t0001g0183a0001c0002t0001g0001a0001c0002t0001g0025others(129): Show | 133 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.11824-528_11824-52 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071237 | ||||||
| chr13:77071237
|
G | GTATA | 78 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(75): Show | 78 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.11824-530_11824-52 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071237 | ||||||
| chr13:77071237
|
G | GTATATA | 45 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(42): Show | 45 | HG00099.hp2 HG00438.hp2 HG01255.hp2 others(42): Show |
intron_variant | MODIFIER | c.11824-532_11824-52 others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071237 | ||||||
| chr13:77071237
|
G | GTATATAT others(1): Show |
3 | a0001c0001t0001g0233a0001c0003t0001g0021a0001c0004t0001g0287 | 3 | HG02630.hp1 HG02717.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.11824-534_11824-52 others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071237 | ||||||
| chr13:77071237
|
G | GTGTA | 72 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(69): Show | 72 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.11824-527_11824-52 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071237 | ||||||
| chr13:77071271
|
G | GCA | 35 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(32): Show | 35 | HG00423.hp2 HG00621.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.11824-562_11824-56 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071271 | ||||||
| chr13:77071271
|
G | GCACA | 42 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.11824-564_11824-56 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071271 | ||||||
| chr13:77071271
|
G | GCACACA | 36 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0094others(33): Show | 36 | HG00280.hp2 HG01106.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.11824-566_11824-56 others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071271 | ||||||
| chr13:77071271
|
G | GCACACAC others(1): Show |
30 | a0001c0001t0001g0007a0001c0001t0001g0089a0001c0001t0001g0091others(27): Show | 30 | HG00099.hp1 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.11824-568_11824-56 others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071271 | ||||||
| chr13:77071271
|
G | GCACACAC others(3): Show |
10 | a0001c0001t0001g0034a0001c0001t0001g0280a0001c0001t0001g0286others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.11824-570_11824-56 others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071271 | ||||||
| chr13:77071271
|
G | GCACACAC others(5): Show |
4 | a0001c0001t0001g0085a0001c0001t0001g0211a0001c0001t0001g0282others(1): Show | 4 | HG01099.hp1 HG02145.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.11824-572_11824-56 others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071271 | ||||||
| chr13:77071271
|
G | GCACACAC others(9): Show |
1 | a0001c0001t0001g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.11824-576_11824-56 others(20): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071271 | ||||||
| chr13:77071271
|
GCA | G | 82 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(79): Show | 83 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.11824-562_11824-56 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071271 | ||||||
| chr13:77071271
|
GCACA | G | 7 | a0001c0002t0002g0053a0001c0003t0001g0014a0001c0003t0001g0044others(4): Show | 7 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.11824-564_11824-56 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071271 | ||||||
| chr13:77071271
|
GCACACA | G | 4 | a0001c0006t0001g0317a0001c0006t0001g0318a0001c0006t0001g0330others(1): Show | 4 | HG00642.hp2 HG01069.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.11824-566_11824-56 others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071271 | ||||||
| chr13:77071273
|
A | G | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.11824-562T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071273 | ||||||
| chr13:77071275
|
A | G | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.11824-564T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071275 | ||||||
| chr13:77071308
|
C | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.11824-597G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071308 | ||||||
| chr13:77071310
|
A | C | 17 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(14): Show | 17 | HG00735.hp2 HG02109.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.11824-599T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071310 | ||||||
| chr13:77071500
|
A | G | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.11824-789T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071500 | ||||||
| chr13:77071736
|
T | C | 36 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(33): Show | 36 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.11824-1025A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071736 | ||||||
| chr13:77071867
|
G | A | 36 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(33): Show | 36 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.11824-1156C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071867 | ||||||
| chr13:77071917
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.11824-1206T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77071917 | ||||||
| chr13:77072102
|
C | T | 11 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG02027.hp2 HG02071.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.11824-1391G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072102 | ||||||
| chr13:77072208
|
G | A | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.11824-1497C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072208 | ||||||
| chr13:77072216
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.11824-1505T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072216 | ||||||
| chr13:77072255
|
C | T | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.11824-1544G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072255 | ||||||
| chr13:77072267
|
G | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.11824-1556C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072267 | ||||||
| chr13:77072300
|
G | A | 2 | a0001c0001t0001g0276a0001c0019t0001g0274 | 2 | HG02155.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.11824-1589C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072300 | ||||||
| chr13:77072300
|
GA | G | 176 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(173): Show | 176 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.11824-1590delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072300 | ||||||
| chr13:77072300
|
GAA | G | 56 | a0001c0001t0001g0085a0001c0001t0001g0163a0001c0001t0001g0173others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.11824-1591_11824-1 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072300 | ||||||
| chr13:77072300
|
GAAAA | G | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.11824-1593_11824-1 others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072300 | ||||||
| chr13:77072301
|
A | G | 2 | a0001c0001t0001g0276a0001c0019t0001g0274 | 2 | HG02155.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.11824-1590T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072301 | ||||||
| chr13:77072323
|
C | CA | 244 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.11824-1613dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072323 | ||||||
| chr13:77072329
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.11824-1618C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072329 | ||||||
| chr13:77072383
|
C | T | 1 | a0001c0005t0002g0136 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.11824-1672G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072383 | ||||||
| chr13:77072419
|
G | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.11824-1708C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072419 | ||||||
| chr13:77072552
|
T | A | 11 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(8): Show | 11 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.11824-1841A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072552 | ||||||
| chr13:77072556
|
G | A | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.11824-1845C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072556 | ||||||
| chr13:77072954
|
C | T | 243 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.11824-2243G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77072954 | ||||||
| chr13:77073025
|
T | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.11824-2314A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77073025 | ||||||
| chr13:77073026
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.11824-2315G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77073026 | ||||||
| chr13:77073114
|
T | C | 52 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(49): Show | 52 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.11824-2403A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77073114 | ||||||
| chr13:77073425
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.11824-2714C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77073425 | ||||||
| chr13:77073479
|
C | T | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.11824-2768G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77073479 | ||||||
| chr13:77073635
|
A | G | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.11824-2924T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77073635 | ||||||
| chr13:77073865
|
G | C | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.11823+2886C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77073865 | ||||||
| chr13:77073899
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.11823+2852A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77073899 | ||||||
| chr13:77074002
|
G | GC | 75 | a0001c0001t0001g0010a0001c0001t0001g0085a0001c0001t0001g0140others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.11823+2748dupG | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074002 | ||||||
| chr13:77074002
|
G | GCC | 29 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0143others(26): Show | 29 | HG00423.hp1 HG01256.hp2 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.11823+2747_11823+2 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074002 | ||||||
| chr13:77074002
|
GC | G | 86 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(83): Show | 86 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.11823+2748delG | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074002 | ||||||
| chr13:77074008
|
C | T | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.11823+2743G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074008 | ||||||
| chr13:77074010
|
C | G | 12 | a0001c0003t0001g0014a0001c0003t0001g0028a0001c0003t0001g0029others(9): Show | 12 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.11823+2741G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074010 | ||||||
| chr13:77074011
|
C | T | 2 | a0001c0006t0001g0322a0001c0045t0001g0327 | 2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.11823+2740G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074011 | ||||||
| chr13:77074012
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.11823+2739G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074012 | ||||||
| chr13:77074019
|
T | C | 4 | a0001c0006t0001g0323a0001c0006t0001g0324a0001c0006t0001g0325others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.11823+2732A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074019 | ||||||
| chr13:77074251
|
G | A | 1 | a0001c0004t0001g0279 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.11823+2500C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074251 | ||||||
| chr13:77074263
|
T | C | 2 | a0001c0001t0001g0286a0001c0001t0001g0300 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.11823+2488A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074263 | ||||||
| chr13:77074727
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.11823+2024G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074727 | ||||||
| chr13:77074808
|
C | T | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.11823+1943G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074808 | ||||||
| chr13:77074961
|
C | A | 2 | a0001c0002t0001g0121a0001c0002t0001g0122 | 2 | NA19085.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.11823+1790G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074961 | ||||||
| chr13:77074985
|
G | A | 18 | a0001c0003t0001g0014a0001c0003t0001g0028a0001c0003t0001g0029others(15): Show | 18 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.11823+1766C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77074985 | ||||||
| chr13:77075077
|
G | A | 1 | a0001c0002t0001g0123 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.11823+1674C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77075077 | ||||||
| chr13:77075179
|
T | C | 1 | a0004c0011t0001g0148 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.11823+1572A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77075179 | ||||||
| chr13:77075193
|
G | A | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.11823+1558C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77075193 | ||||||
| chr13:77075385
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.11823+1366A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77075385 | ||||||
| chr13:77075490
|
T | C | 12 | a0001c0003t0001g0014a0001c0003t0001g0028a0001c0003t0001g0029others(9): Show | 12 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.11823+1261A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77075490 | ||||||
| chr13:77075587
|
A | G | 1 | a0001c0004t0001g0087 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.11823+1164T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77075587 | ||||||
| chr13:77075607
|
C | T | 20 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(17): Show | 20 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.11823+1144G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77075607 | ||||||
| chr13:77075675
|
G | T | 1 | a0001c0002t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.11823+1076C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77075675 | ||||||
| chr13:77075680
|
G | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.11823+1071C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77075680 | ||||||
| chr13:77076059
|
C | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.11823+692G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77076059 | ||||||
| chr13:77076218
|
C | T | 1 | a0001c0003t0001g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.11823+533G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77076218 | ||||||
| chr13:77076421
|
T | C | 3 | a0001c0006t0001g0319a0001c0006t0001g0320a0001c0006t0001g0322 | 3 | HG01891.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.11823+330A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77076421 | ||||||
| chr13:77076515
|
A | G | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.11823+236T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 68/82 | chr13 | 77076515 | ||||||
| chr13:77076983
|
T | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0247 | 2 | HG00597.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.11725-134A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 67/82 | chr13 | 77076983 | ||||||
| chr13:77077025
|
G | GA | 19 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.11724+122dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 67/82 | chr13 | 77077025 | ||||||
| chr13:77077060
|
G | A | 19 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.11724+88C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 67/82 | chr13 | 77077060 | ||||||
| chr13:77077090
|
C | T | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.11724+58G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 67/82 | chr13 | 77077090 | ||||||
| chr13:77077603
|
T | C | 326 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.11485-216A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 66/82 | chr13 | 77077603 | ||||||
| chr13:77077676
|
G | A | 2 | a0001c0002t0001g0171a0001c0003t0001g0295 | 2 | HG02970.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.11485-289C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 66/82 | chr13 | 77077676 | ||||||
| chr13:77077787
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.11485-400G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 66/82 | chr13 | 77077787 | ||||||
| chr13:77077870
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.11485-483G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 66/82 | chr13 | 77077870 | ||||||
| chr13:77078075
|
G | C | 7 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(4): Show | 7 | HG00621.hp1 HG02132.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.11485-688C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 66/82 | chr13 | 77078075 | ||||||
| chr13:77078775
|
G | A | 1 | a0001c0004t0001g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.11484+49C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 66/82 | chr13 | 77078775 | ||||||
| chr13:77078946
|
A | G | 45 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 45 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(42): Show |
intron_variant | MODIFIER | c.11419-57T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77078946 | ||||||
| chr13:77079016
|
C | T | 3 | a0001c0002t0001g0036a0001c0002t0001g0039a0001c0002t0001g0040 | 3 | HG00280.hp1 HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.11419-127G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77079016 | ||||||
| chr13:77079042
|
G | A | 1 | a0001c0002t0001g0171 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.11419-153C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77079042 | ||||||
| chr13:77079562
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.11419-673A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77079562 | ||||||
| chr13:77079573
|
A | C | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.11419-684T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77079573 | ||||||
| chr13:77079670
|
A | G | 109 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(106): Show | 109 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.11419-781T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77079670 | ||||||
| chr13:77079814
|
A | G | 1 | a0014c0032t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.11419-925T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77079814 | ||||||
| chr13:77080014
|
C | A | 45 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 45 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(42): Show |
intron_variant | MODIFIER | c.11419-1125G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77080014 | ||||||
| chr13:77080059
|
C | G | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.11419-1170G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77080059 | ||||||
| chr13:77080289
|
C | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.11418+1138G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77080289 | ||||||
| chr13:77080427
|
T | C | 8 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(5): Show | 8 | NA18946.hp1 NA18966.hp2 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.11418+1000A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77080427 | ||||||
| chr13:77080745
|
C | T | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0073others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.11418+682G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77080745 | ||||||
| chr13:77080942
|
G | GA | 52 | a0001c0001t0001g0170a0001c0002t0001g0056a0001c0003t0001g0015others(49): Show | 52 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.11418+484dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77080942 | ||||||
| chr13:77081088
|
A | G | 331 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.11418+339T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77081088 | ||||||
| chr13:77081399
|
G | C | 1 | a0001c0002t0001g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.11418+28C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77081399 | ||||||
| chr13:77081408
|
A | G | 1 | a0001c0003t0001g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.11418+19T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77081408 | ||||||
| chr13:77081413
|
G | A | 45 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(42): Show | 45 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(42): Show |
intron_variant | MODIFIER | c.11418+14C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 65/82 | chr13 | 77081413 | ||||||
| chr13:77081762
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.11193+75A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 64/82 | chr13 | 77081762 | ||||||
| chr13:77082003
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.11037-10G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/82 | chr13 | 77082003 | ||||||
| chr13:77082021
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.11037-28G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/82 | chr13 | 77082021 | ||||||
| chr13:77082022
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0280 | 2 | HG01255.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.11037-29C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/82 | chr13 | 77082022 | ||||||
| chr13:77082050
|
G | A | 6 | a0001c0002t0001g0052a0001c0002t0001g0054a0001c0002t0001g0055others(3): Show | 6 | HG00609.hp2 HG02155.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.11037-57C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/82 | chr13 | 77082050 | ||||||
| chr13:77082068
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.11037-75G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/82 | chr13 | 77082068 | ||||||
| chr13:77082187
|
C | T | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.11037-194G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/82 | chr13 | 77082187 | ||||||
| chr13:77082225
|
T | C | 3 | a0001c0005t0002g0138a0001c0005t0002g0223a0001c0005t0002g0271 | 3 | HG00099.hp1 NA18995.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.11037-232A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/82 | chr13 | 77082225 | ||||||
| chr13:77082501
|
T | C | 1 | a0001c0003t0001g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.11037-508A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/82 | chr13 | 77082501 | ||||||
| chr13:77082919
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.11036+113A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/82 | chr13 | 77082919 | ||||||
| chr13:77083016
|
T | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.11036+16A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/82 | chr13 | 77083016 | ||||||
| chr13:77083022
|
C | A | 1 | a0001c0002t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.11036+10G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 63/82 | chr13 | 77083022 | ||||||
| chr13:77083263
|
T | C | 36 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(33): Show | 36 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.10876-71A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77083263 | ||||||
| chr13:77083421
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.10876-229C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77083421 | ||||||
| chr13:77083535
|
A | G | 1 | a0001c0002t0001g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.10876-343T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77083535 | ||||||
| chr13:77083871
|
C | T | 1 | a0001c0008t0001g0308 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.10876-679G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77083871 | ||||||
| chr13:77084725
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.10876-1533A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77084725 | ||||||
| chr13:77084862
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10876-1670T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77084862 | ||||||
| chr13:77084927
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.10876-1735C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77084927 | ||||||
| chr13:77084951
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.10876-1759T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77084951 | ||||||
| chr13:77085049
|
G | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.10876-1857C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77085049 | ||||||
| chr13:77085216
|
C | T | 13 | a0001c0002t0001g0001a0001c0002t0001g0104a0001c0002t0001g0114others(10): Show | 14 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.10876-2024G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77085216 | ||||||
| chr13:77085300
|
TGGTGGGA others(7): Show |
T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.10876-2122_10876-2 others(20): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77085300 | ||||||
| chr13:77085391
|
T | G | 1 | a0002c0007t0001g0218 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.10875+2093A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77085391 | ||||||
| chr13:77085575
|
G | A | 3 | a0004c0011t0001g0148a0004c0011t0001g0152a0004c0011t0001g0156 | 3 | NA18950.hp2 NA18994.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.10875+1909C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77085575 | ||||||
| chr13:77085814
|
C | A | 1 | a0006c0017t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.10875+1670G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77085814 | ||||||
| chr13:77086031
|
A | G | 1 | a0001c0002t0001g0288 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.10875+1453T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77086031 | ||||||
| chr13:77086269
|
A | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.10875+1215T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77086269 | ||||||
| chr13:77086328
|
T | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10875+1156A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77086328 | ||||||
| chr13:77086329
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10875+1155C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77086329 | ||||||
| chr13:77086331
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10875+1153G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77086331 | ||||||
| chr13:77086332
|
C | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10875+1152G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77086332 | ||||||
| chr13:77086333
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10875+1151G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77086333 | ||||||
| chr13:77086418
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.10875+1066A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77086418 | ||||||
| chr13:77086632
|
T | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.10875+852A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77086632 | ||||||
| chr13:77086760
|
G | A | 2 | a0001c0008t0001g0263a0001c0008t0001g0296 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.10875+724C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77086760 | ||||||
| chr13:77086911
|
C | T | 206 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.10875+573G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77086911 | ||||||
| chr13:77087069
|
CTT | C | 6 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0093others(3): Show | 6 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.10875+413_10875+41 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77087069 | ||||||
| chr13:77087243
|
T | C | 20 | a0001c0004t0001g0087a0001c0004t0001g0088a0001c0004t0001g0150others(17): Show | 20 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.10875+241A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77087243 | ||||||
| chr13:77087393
|
C | T | 109 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(106): Show | 109 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.10875+91G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 62/82 | chr13 | 77087393 | ||||||
| chr13:77087718
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10726-85T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 61/82 | chr13 | 77087718 | ||||||
| chr13:77087818
|
T | C | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.10726-185A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 61/82 | chr13 | 77087818 | ||||||
| chr13:77087846
|
T | C | 1 | a0001c0043t0001g0292 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.10726-213A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 61/82 | chr13 | 77087846 | ||||||
| chr13:77087956
|
C | T | 5 | a0001c0002t0001g0052a0001c0002t0001g0054a0001c0002t0001g0055others(2): Show | 5 | HG00609.hp2 HG02155.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.10726-323G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 61/82 | chr13 | 77087956 | ||||||
| chr13:77087994
|
C | T | 7 | a0001c0001t0001g0034a0001c0001t0001g0163a0001c0001t0001g0173others(4): Show | 7 | HG00738.hp1 HG01255.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.10726-361G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 61/82 | chr13 | 77087994 | ||||||
| chr13:77088025
|
C | T | 1 | a0016c0028t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.10726-392G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 61/82 | chr13 | 77088025 | ||||||
| chr13:77088304
|
G | C | 1 | a0006c0017t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.10725+528C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 61/82 | chr13 | 77088304 | ||||||
| chr13:77088708
|
T | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10725+124A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 61/82 | chr13 | 77088708 | ||||||
| chr13:77088766
|
G | A | 12 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(9): Show | 12 | HG00099.hp1 NA18946.hp1 NA18966.hp2 others(9): Show |
intron_variant | MODIFIER | c.10725+66C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 61/82 | chr13 | 77088766 | ||||||
| chr13:77088774
|
G | A | 1 | a0001c0004t0001g0087 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.10725+58C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 61/82 | chr13 | 77088774 | ||||||
| chr13:77089223
|
T | C | 1 | a0001c0002t0001g0201 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.10526-192A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 60/82 | chr13 | 77089223 | ||||||
| chr13:77089611
|
G | A | 61 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0089others(58): Show | 61 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.10525+495C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 60/82 | chr13 | 77089611 | ||||||
| chr13:77089625
|
A | G | 36 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(33): Show | 36 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.10525+481T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 60/82 | chr13 | 77089625 | ||||||
| chr13:77089646
|
T | TC | 4 | a0001c0003t0001g0033a0001c0003t0001g0207a0001c0003t0006g0209others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.10525+459_10525+46 others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 60/82 | chr13 | 77089646 | ||||||
| chr13:77089646
|
TG | T | 12 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(9): Show | 12 | HG00544.hp2 HG01069.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.10525+459delC | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 60/82 | chr13 | 77089646 | ||||||
| chr13:77089647
|
G | C | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(313): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.10525+459C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 60/82 | chr13 | 77089647 | ||||||
| chr13:77089647
|
G | T | 4 | a0001c0003t0001g0033a0001c0003t0001g0207a0001c0003t0006g0209others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.10525+459C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 60/82 | chr13 | 77089647 | ||||||
| chr13:77089648
|
T | C | 12 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(9): Show | 12 | HG00544.hp2 HG01069.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.10525+458A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 60/82 | chr13 | 77089648 | ||||||
| chr13:77089777
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10525+329G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 60/82 | chr13 | 77089777 | ||||||
| chr13:77089881
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10525+225G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 60/82 | chr13 | 77089881 | ||||||
| chr13:77090493
|
T | C | 20 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(17): Show | 20 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.10368-230A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77090493 | ||||||
| chr13:77090540
|
A | G | 1 | a0001c0001t0003g0003 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.10368-277T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77090540 | ||||||
| chr13:77090622
|
A | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.10368-359T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77090622 | ||||||
| chr13:77090633
|
T | C | 1 | a0001c0002t0002g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.10368-370A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77090633 | ||||||
| chr13:77090849
|
T | A | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.10368-586A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77090849 | ||||||
| chr13:77090915
|
A | G | 1 | a0001c0006t0001g0322 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.10368-652T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77090915 | ||||||
| chr13:77091033
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.10368-770G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77091033 | ||||||
| chr13:77091045
|
T | C | 4 | a0001c0001t0001g0282a0001c0001t0001g0286a0001c0001t0001g0294others(1): Show | 4 | HG00280.hp2 HG03017.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.10368-782A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77091045 | ||||||
| chr13:77091129
|
T | C | 73 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(70): Show | 73 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.10368-866A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77091129 | ||||||
| chr13:77091130
|
ATCTATTT others(13): Show |
A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.10368-887_10368-86 others(24): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77091130 | ||||||
| chr13:77091379
|
T | G | 1 | a0009c0022t0005g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.10368-1116A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77091379 | ||||||
| chr13:77091429
|
C | CA | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0235others(18): Show | 21 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.10368-1167dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77091429 | ||||||
| chr13:77091644
|
A | G | 3 | a0002c0007t0001g0212a0002c0007t0001g0217a0002c0007t0001g0219 | 3 | HG02486.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.10368-1381T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77091644 | ||||||
| chr13:77091740
|
T | C | 332 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.10367+1425A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77091740 | ||||||
| chr13:77091871
|
G | A | 11 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(8): Show | 11 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.10367+1294C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77091871 | ||||||
| chr13:77091899
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10367+1266T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77091899 | ||||||
| chr13:77091998
|
G | A | 1 | a0001c0031t0001g0070 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.10367+1167C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77091998 | ||||||
| chr13:77092026
|
T | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10367+1139A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77092026 | ||||||
| chr13:77092041
|
C | A | 87 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(84): Show | 88 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.10367+1124G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77092041 | ||||||
| chr13:77092081
|
G | GA | 293 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(290): Show | 294 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.10367+1083dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77092081 | ||||||
| chr13:77092081
|
G | GAA | 29 | a0001c0001t0001g0080a0001c0001t0001g0175a0001c0001t0001g0228others(26): Show | 29 | HG00099.hp1 HG00741.hp1 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.10367+1082_10367+1 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77092081 | ||||||
| chr13:77092123
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10367+1042G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77092123 | ||||||
| chr13:77092330
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.10367+835G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77092330 | ||||||
| chr13:77092550
|
G | A | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.10367+615C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77092550 | ||||||
| chr13:77092672
|
C | T | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.10367+493G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77092672 | ||||||
| chr13:77092776
|
C | T | 1 | a0001c0002t0001g0026 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.10367+389G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77092776 | ||||||
| chr13:77092960
|
A | G | 1 | a0001c0006t0001g0321 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.10367+205T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77092960 | ||||||
| chr13:77093116
|
T | C | 1 | a0001c0004t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.10367+49A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77093116 | ||||||
| chr13:77093161
|
A | G | 1 | a0010c0025t0001g0086 | 1 | HG02970.hp1 | splice_region_variant&intron_variant | LOW | c.10367+4T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 59/82 | chr13 | 77093161 | ||||||
| chr13:77093404
|
A | G | 1 | a0002c0040t0001g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.10200-72T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77093404 | ||||||
| chr13:77093953
|
T | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(107): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.10200-621A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77093953 | ||||||
| chr13:77094111
|
C | A | 3 | a0001c0004t0001g0088a0001c0004t0001g0151a0001c0004t0001g0174 | 3 | HG02258.hp1 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.10200-779G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77094111 | ||||||
| chr13:77094299
|
T | C | 1 | a0001c0004t0001g0287 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.10200-967A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77094299 | ||||||
| chr13:77094316
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.10200-984A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77094316 | ||||||
| chr13:77094521
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.10199+837G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77094521 | ||||||
| chr13:77094690
|
C | T | 12 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(9): Show | 12 | HG00544.hp1 HG02015.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.10199+668G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77094690 | ||||||
| chr13:77094905
|
T | C | 1 | a0001c0044t0001g0332 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.10199+453A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77094905 | ||||||
| chr13:77094918
|
T | C | 2 | a0001c0003t0001g0264a0001c0030t0001g0037 | 2 | HG01981.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.10199+440A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77094918 | ||||||
| chr13:77095191
|
A | G | 1 | a0001c0002t0001g0201 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.10199+167T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77095191 | ||||||
| chr13:77095272
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.10199+86C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77095272 | ||||||
| chr13:77095282
|
C | T | 1 | a0001c0020t0001g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.10199+76G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77095282 | ||||||
| chr13:77095290
|
C | T | 12 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0073others(9): Show | 12 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.10199+68G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 58/82 | chr13 | 77095290 | ||||||
| chr13:77095629
|
C | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(2): Show | 5 | HG02165.hp2 NA18974.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.9955-27G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 57/82 | chr13 | 77095629 | ||||||
| chr13:77095892
|
G | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.9955-290C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 57/82 | chr13 | 77095892 | ||||||
| chr13:77095954
|
A | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.9955-352T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 57/82 | chr13 | 77095954 | ||||||
| chr13:77095971
|
A | C | 1 | a0001c0001t0001g0141 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.9954+341T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 57/82 | chr13 | 77095971 | ||||||
| chr13:77096082
|
A | C | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.9954+230T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 57/82 | chr13 | 77096082 | ||||||
| chr13:77096099
|
G | A | 1 | a0002c0007t0001g0219 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.9954+213C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 57/82 | chr13 | 77096099 | ||||||
| chr13:77096168
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.9954+144T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 57/82 | chr13 | 77096168 | ||||||
| chr13:77096660
|
A | T | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.9785-179T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/82 | chr13 | 77096660 | ||||||
| chr13:77096851
|
T | C | 1 | a0001c0001t0001g0315 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.9785-370A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/82 | chr13 | 77096851 | ||||||
| chr13:77096919
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0294 | 2 | HG00280.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.9785-438C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/82 | chr13 | 77096919 | ||||||
| chr13:77096930
|
A | G | 2 | a0001c0001t0004g0181a0001c0001t0004g0184 | 2 | NA18942.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.9784+440T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/82 | chr13 | 77096930 | ||||||
| chr13:77096937
|
G | GA | 22 | a0001c0002t0001g0259a0001c0005t0002g0078a0001c0005t0002g0079others(19): Show | 22 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.9784+432dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/82 | chr13 | 77096937 | ||||||
| chr13:77097064
|
T | C | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.9784+306A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/82 | chr13 | 77097064 | ||||||
| chr13:77097086
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.9784+284G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/82 | chr13 | 77097086 | ||||||
| chr13:77097196
|
T | C | 105 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(102): Show | 105 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.9784+174A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/82 | chr13 | 77097196 | ||||||
| chr13:77097271
|
T | C | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0304 | 3 | HG00673.hp2 NA18945.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.9784+99A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 56/82 | chr13 | 77097271 | ||||||
| chr13:77099369
|
G | T | 1 | a0001c0003t0001g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8141-356C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77099369 | ||||||
| chr13:77099433
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-420T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77099433 | ||||||
| chr13:77099529
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.8141-516T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77099529 | ||||||
| chr13:77099595
|
T | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.8141-582A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77099595 | ||||||
| chr13:77099654
|
A | C | 1 | a0001c0003t0001g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8141-641T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77099654 | ||||||
| chr13:77099710
|
A | T | 1 | a0001c0003t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.8141-697T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77099710 | ||||||
| chr13:77100019
|
A | G | 1 | a0001c0002t0001g0123 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.8141-1006T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77100019 | ||||||
| chr13:77100164
|
T | G | 1 | a0015c0027t0007g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.8141-1151A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77100164 | ||||||
| chr13:77100246
|
C | T | 1 | a0001c0004t0001g0150 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.8141-1233G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77100246 | ||||||
| chr13:77100278
|
G | A | 1 | a0001c0002t0001g0108 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.8141-1265C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77100278 | ||||||
| chr13:77100291
|
A | G | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.8141-1278T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77100291 | ||||||
| chr13:77100324
|
C | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.8141-1311G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77100324 | ||||||
| chr13:77101107
|
G | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.8141-2094C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77101107 | ||||||
| chr13:77101405
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-2392A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77101405 | ||||||
| chr13:77101567
|
G | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.8141-2554C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77101567 | ||||||
| chr13:77101747
|
G | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0300 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.8141-2734C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77101747 | ||||||
| chr13:77101880
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.8141-2867A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77101880 | ||||||
| chr13:77101936
|
C | T | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.8141-2923G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77101936 | ||||||
| chr13:77102053
|
G | C | 5 | a0001c0001t0001g0238a0001c0001t0003g0002a0001c0001t0003g0003others(2): Show | 5 | NA18942.hp1 NA18952.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.8141-3040C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77102053 | ||||||
| chr13:77102132
|
A | AT | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.8141-3120dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77102132 | ||||||
| chr13:77102171
|
T | G | 1 | a0001c0002t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.8141-3158A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77102171 | ||||||
| chr13:77102928
|
C | T | 1 | a0001c0002t0001g0054 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.8141-3915G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77102928 | ||||||
| chr13:77102982
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.8141-3969A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77102982 | ||||||
| chr13:77102994
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-3981A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77102994 | ||||||
| chr13:77103039
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.8141-4026A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77103039 | ||||||
| chr13:77103075
|
A | G | 9 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(6): Show | 9 | NA18946.hp1 NA18966.hp2 NA18977.hp1 others(6): Show |
intron_variant | MODIFIER | c.8141-4062T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77103075 | ||||||
| chr13:77103139
|
C | G | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.8141-4126G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77103139 | ||||||
| chr13:77103139
|
C | T | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.8141-4126G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77103139 | ||||||
| chr13:77103377
|
C | T | 1 | a0001c0004t0001g0088 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8141-4364G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77103377 | ||||||
| chr13:77103795
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.8141-4782C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77103795 | ||||||
| chr13:77104019
|
C | CT | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.8141-5007dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77104019 | ||||||
| chr13:77104223
|
A | G | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.8141-5210T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77104223 | ||||||
| chr13:77104264
|
T | C | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.8141-5251A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77104264 | ||||||
| chr13:77104339
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.8141-5326G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77104339 | ||||||
| chr13:77104397
|
A | G | 20 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(17): Show | 20 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.8141-5384T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77104397 | ||||||
| chr13:77104398
|
T | C | 20 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(17): Show | 20 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.8141-5385A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77104398 | ||||||
| chr13:77104497
|
G | A | 4 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(1): Show | 4 | NA18942.hp1 NA18957.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.8141-5484C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77104497 | ||||||
| chr13:77104731
|
G | C | 1 | a0001c0003t0001g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.8141-5718C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77104731 | ||||||
| chr13:77105022
|
A | G | 1 | a0002c0040t0001g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.8141-6009T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77105022 | ||||||
| chr13:77105076
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-6063G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77105076 | ||||||
| chr13:77105189
|
C | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.8141-6176G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77105189 | ||||||
| chr13:77105367
|
T | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-6354A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77105367 | ||||||
| chr13:77105618
|
GA | G | 11 | a0001c0003t0001g0035a0001c0003t0001g0129a0001c0009t0001g0076others(8): Show | 11 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.8141-6606delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77105618 | ||||||
| chr13:77105752
|
C | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0164others(1): Show | 4 | HG01243.hp2 HG01261.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.8141-6739G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77105752 | ||||||
| chr13:77105803
|
C | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.8141-6790G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77105803 | ||||||
| chr13:77105828
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.8141-6815A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77105828 | ||||||
| chr13:77106103
|
T | C | 1 | a0001c0002t0001g0058 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.8141-7090A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77106103 | ||||||
| chr13:77106230
|
G | A | 1 | a0001c0004t0001g0287 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.8141-7217C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77106230 | ||||||
| chr13:77106380
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.8141-7367A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77106380 | ||||||
| chr13:77106582
|
A | G | 1 | a0001c0003t0001g0072 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.8141-7569T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77106582 | ||||||
| chr13:77106728
|
T | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-7715A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77106728 | ||||||
| chr13:77106735
|
T | C | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.8141-7722A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77106735 | ||||||
| chr13:77106740
|
T | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-7727A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77106740 | ||||||
| chr13:77106780
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.8141-7767T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77106780 | ||||||
| chr13:77106924
|
T | C | 1 | a0001c0003t0001g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.8141-7911A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77106924 | ||||||
| chr13:77107016
|
T | A | 1 | a0001c0002t0001g0055 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.8141-8003A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77107016 | ||||||
| chr13:77107026
|
T | C | 2 | a0001c0005t0002g0078a0001c0005t0002g0079 | 2 | NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.8141-8013A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77107026 | ||||||
| chr13:77107115
|
A | C | 1 | a0012c0038t0002g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.8141-8102T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77107115 | ||||||
| chr13:77107630
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.8141-8617G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77107630 | ||||||
| chr13:77107716
|
C | A | 1 | a0001c0001t0001g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.8141-8703G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77107716 | ||||||
| chr13:77107867
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.8141-8854A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77107867 | ||||||
| chr13:77107977
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-8964A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77107977 | ||||||
| chr13:77108373
|
A | G | 28 | a0001c0004t0001g0087a0001c0004t0001g0088a0001c0004t0001g0150others(25): Show | 28 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.8141-9360T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108373 | ||||||
| chr13:77108534
|
A | G | 1 | a0001c0006t0001g0319 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.8141-9521T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108534 | ||||||
| chr13:77108643
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-9630C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108643 | ||||||
| chr13:77108685
|
C | G | 34 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(31): Show | 34 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.8141-9672G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108685 | ||||||
| chr13:77108705
|
A | AT | 9 | a0001c0003t0001g0016a0001c0003t0001g0028a0001c0003t0001g0029others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.8141-9693dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108705 | ||||||
| chr13:77108705
|
AT | A | 10 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(7): Show | 10 | HG00735.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.8141-9693delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108705 | ||||||
| chr13:77108708
|
T | A | 2 | a0001c0002t0001g0057a0001c0002t0001g0062 | 2 | NA18981.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.8141-9695A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108708 | ||||||
| chr13:77108708
|
T | TA | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.8141-9696_8141-969 others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108708 | ||||||
| chr13:77108709
|
T | A | 37 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(34): Show | 37 | HG00438.hp2 HG00597.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.8141-9696A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108709 | ||||||
| chr13:77108711
|
T | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-9698A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108711 | ||||||
| chr13:77108815
|
C | T | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.8141-9802G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108815 | ||||||
| chr13:77108894
|
G | A | 1 | a0009c0022t0005g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.8141-9881C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108894 | ||||||
| chr13:77108922
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.8141-9909G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108922 | ||||||
| chr13:77108939
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.8141-9926G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77108939 | ||||||
| chr13:77109075
|
C | T | 2 | a0001c0002t0001g0119a0001c0002t0001g0149 | 2 | NA18955.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.8141-10062G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77109075 | ||||||
| chr13:77109136
|
T | C | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8141-10123A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77109136 | ||||||
| chr13:77109257
|
G | A | 50 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(47): Show | 50 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.8141-10244C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77109257 | ||||||
| chr13:77109266
|
C | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-10253G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77109266 | ||||||
| chr13:77109429
|
C | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-10416G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77109429 | ||||||
| chr13:77109528
|
C | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.8141-10515G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77109528 | ||||||
| chr13:77109706
|
T | G | 1 | a0001c0009t0001g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.8141-10693A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77109706 | ||||||
| chr13:77109712
|
G | A | 1 | a0001c0009t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.8141-10699C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77109712 | ||||||
| chr13:77109739
|
A | T | 1 | a0001c0003t0001g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.8141-10726T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77109739 | ||||||
| chr13:77109814
|
T | C | 1 | a0001c0006t0001g0321 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.8141-10801A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77109814 | ||||||
| chr13:77110001
|
T | C | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8141-10988A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110001 | ||||||
| chr13:77110013
|
CAT | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.8141-11002_8141-11 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110013 | ||||||
| chr13:77110116
|
C | T | 1 | a0001c0002t0001g0123 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.8141-11103G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110116 | ||||||
| chr13:77110149
|
C | T | 1 | a0001c0004t0001g0155 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.8141-11136G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110149 | ||||||
| chr13:77110180
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8141-11167A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110180 | ||||||
| chr13:77110219
|
A | G | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.8140+11154T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110219 | ||||||
| chr13:77110247
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.8140+11126A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110247 | ||||||
| chr13:77110274
|
C | T | 22 | a0001c0003t0001g0042a0001c0005t0002g0078a0001c0005t0002g0079others(19): Show | 22 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.8140+11099G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110274 | ||||||
| chr13:77110369
|
AAAACCCC others(5): Show |
A | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.8140+10992_8140+11 others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110369 | ||||||
| chr13:77110402
|
G | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.8140+10971C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110402 | ||||||
| chr13:77110432
|
T | C | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.8140+10941A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110432 | ||||||
| chr13:77110660
|
G | A | 5 | a0002c0007t0001g0213a0002c0007t0001g0214a0002c0007t0001g0215others(2): Show | 5 | HG00735.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.8140+10713C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110660 | ||||||
| chr13:77110774
|
C | T | 3 | a0001c0002t0001g0026a0005c0015t0001g0113a0005c0015t0001g0258 | 3 | HG00544.hp2 NA19012.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.8140+10599G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110774 | ||||||
| chr13:77110775
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.8140+10598C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110775 | ||||||
| chr13:77110915
|
A | G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.8140+10458T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77110915 | ||||||
| chr13:77111205
|
A | G | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.8140+10168T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111205 | ||||||
| chr13:77111301
|
A | G | 1 | a0001c0003t0001g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8140+10072T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111301 | ||||||
| chr13:77111303
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.8140+10070G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111303 | ||||||
| chr13:77111435
|
C | A | 1 | a0016c0028t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.8140+9938G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111435 | ||||||
| chr13:77111454
|
A | G | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8140+9919T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111454 | ||||||
| chr13:77111552
|
G | A | 1 | a0012c0038t0002g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.8140+9821C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111552 | ||||||
| chr13:77111583
|
AT | A | 205 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.8140+9789delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111583 | ||||||
| chr13:77111634
|
G | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.8140+9739C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111634 | ||||||
| chr13:77111647
|
C | A | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.8140+9726G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111647 | ||||||
| chr13:77111698
|
C | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8140+9675G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111698 | ||||||
| chr13:77111706
|
C | T | 2 | a0001c0003t0001g0260a0001c0003t0001g0261 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.8140+9667G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111706 | ||||||
| chr13:77111878
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.8140+9495G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111878 | ||||||
| chr13:77111898
|
T | C | 20 | a0001c0004t0001g0087a0001c0004t0001g0088a0001c0004t0001g0150others(17): Show | 20 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.8140+9475A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111898 | ||||||
| chr13:77111958
|
G | A | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.8140+9415C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77111958 | ||||||
| chr13:77112173
|
A | C | 88 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(85): Show | 89 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.8140+9200T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77112173 | ||||||
| chr13:77112199
|
C | T | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.8140+9174G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77112199 | ||||||
| chr13:77112289
|
T | TTA | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.8140+9082_8140+908 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77112289 | ||||||
| chr13:77112309
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.8140+9064A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77112309 | ||||||
| chr13:77112373
|
T | C | 89 | a0001c0001t0001g0183a0001c0002t0001g0001a0001c0002t0001g0025others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.8140+9000A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77112373 | ||||||
| chr13:77112604
|
A | T | 1 | a0002c0007t0001g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.8140+8769T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77112604 | ||||||
| chr13:77112605
|
T | A | 2 | a0001c0006t0001g0330a0001c0006t0001g0331 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.8140+8768A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77112605 | ||||||
| chr13:77112827
|
C | G | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.8140+8546G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77112827 | ||||||
| chr13:77113076
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.8140+8297C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77113076 | ||||||
| chr13:77113078
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0283 | 2 | NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.8140+8295T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77113078 | ||||||
| chr13:77113222
|
C | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.8140+8151G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77113222 | ||||||
| chr13:77113298
|
T | C | 76 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(73): Show | 76 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.8140+8075A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77113298 | ||||||
| chr13:77113364
|
G | A | 331 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.8140+8009C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77113364 | ||||||
| chr13:77113456
|
G | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.8140+7917C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77113456 | ||||||
| chr13:77113628
|
A | G | 77 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(74): Show | 77 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.8140+7745T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77113628 | ||||||
| chr13:77113882
|
A | C | 2 | a0001c0009t0001g0310a0001c0009t0001g0311 | 2 | NA18612.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.8140+7491T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77113882 | ||||||
| chr13:77113969
|
C | T | 1 | a0001c0026t0001g0285 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.8140+7404G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77113969 | ||||||
| chr13:77114176
|
A | T | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.8140+7197T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77114176 | ||||||
| chr13:77114409
|
C | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0160a0001c0001t0001g0162others(1): Show | 4 | HG00741.hp2 HG01106.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.8140+6964G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77114409 | ||||||
| chr13:77114503
|
T | C | 1 | a0012c0038t0002g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.8140+6870A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77114503 | ||||||
| chr13:77114606
|
T | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8140+6767A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77114606 | ||||||
| chr13:77114888
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0283 | 2 | NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.8140+6485C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77114888 | ||||||
| chr13:77114993
|
C | T | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.8140+6380G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77114993 | ||||||
| chr13:77115030
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0001g0228 | 2 | NA18998.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.8140+6343A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77115030 | ||||||
| chr13:77115138
|
A | G | 1 | a0001c0023t0001g0206 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.8140+6235T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77115138 | ||||||
| chr13:77115205
|
T | C | 7 | a0001c0004t0001g0087a0001c0004t0001g0153a0001c0004t0001g0240others(4): Show | 7 | HG00621.hp2 NA18946.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.8140+6168A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77115205 | ||||||
| chr13:77115208
|
A | G | 1 | a0001c0031t0001g0070 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.8140+6165T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77115208 | ||||||
| chr13:77115295
|
T | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.8140+6078A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77115295 | ||||||
| chr13:77115351
|
T | A | 3 | a0002c0007t0001g0212a0002c0007t0001g0217a0002c0007t0001g0219 | 3 | HG02486.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.8140+6022A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77115351 | ||||||
| chr13:77115358
|
T | C | 326 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.8140+6015A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77115358 | ||||||
| chr13:77115684
|
G | GA | 15 | a0001c0003t0001g0014a0001c0003t0001g0047a0001c0003t0001g0129others(12): Show | 15 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.8140+5688dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77115684 | ||||||
| chr13:77116066
|
G | A | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.8140+5307C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77116066 | ||||||
| chr13:77116109
|
T | C | 7 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0164others(4): Show | 7 | HG01243.hp2 HG01261.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.8140+5264A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77116109 | ||||||
| chr13:77116140
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8140+5233C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77116140 | ||||||
| chr13:77116206
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.8140+5167A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77116206 | ||||||
| chr13:77116207
|
T | A | 88 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(85): Show | 89 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.8140+5166A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77116207 | ||||||
| chr13:77116452
|
T | C | 6 | a0001c0006t0001g0319a0001c0006t0001g0320a0001c0006t0001g0322others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.8140+4921A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77116452 | ||||||
| chr13:77116464
|
T | A | 1 | a0001c0035t0001g0030 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.8140+4909A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77116464 | ||||||
| chr13:77116547
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8140+4826A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77116547 | ||||||
| chr13:77116563
|
T | C | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.8140+4810A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77116563 | ||||||
| chr13:77116717
|
A | G | 1 | a0001c0019t0001g0274 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.8140+4656T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77116717 | ||||||
| chr13:77117011
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.8140+4362T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77117011 | ||||||
| chr13:77117067
|
C | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012 | 3 | HG01891.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.8140+4306G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77117067 | ||||||
| chr13:77117303
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0283 | 2 | NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.8140+4070A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77117303 | ||||||
| chr13:77117748
|
T | C | 1 | a0002c0007t0001g0218 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.8140+3625A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77117748 | ||||||
| chr13:77117870
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.8140+3503A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77117870 | ||||||
| chr13:77117882
|
A | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.8140+3491T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77117882 | ||||||
| chr13:77118308
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.8140+3065G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77118308 | ||||||
| chr13:77118551
|
G | A | 2 | a0005c0015t0001g0113a0005c0015t0001g0258 | 2 | NA19012.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.8140+2822C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77118551 | ||||||
| chr13:77118665
|
C | T | 104 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(101): Show | 104 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.8140+2708G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77118665 | ||||||
| chr13:77118785
|
C | T | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.8140+2588G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77118785 | ||||||
| chr13:77118797
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8140+2576C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77118797 | ||||||
| chr13:77118892
|
C | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.8140+2481G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77118892 | ||||||
| chr13:77118921
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.8140+2452A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77118921 | ||||||
| chr13:77118995
|
T | C | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.8140+2378A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77118995 | ||||||
| chr13:77119232
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.8140+2141C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77119232 | ||||||
| chr13:77119385
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.8140+1988T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77119385 | ||||||
| chr13:77119462
|
T | G | 2 | a0001c0002t0001g0001a0001c0002t0001g0114 | 3 | HG03490.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.8140+1911A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77119462 | ||||||
| chr13:77119552
|
A | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.8140+1821T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77119552 | ||||||
| chr13:77119601
|
G | A | 1 | a0001c0002t0001g0026 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.8140+1772C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77119601 | ||||||
| chr13:77119865
|
T | C | 3 | a0001c0009t0001g0076a0001c0009t0001g0310a0001c0009t0001g0311 | 3 | HG00621.hp1 NA18612.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.8140+1508A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77119865 | ||||||
| chr13:77119910
|
C | T | 1 | a0001c0002t0001g0059 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.8140+1463G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77119910 | ||||||
| chr13:77120257
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.8140+1116C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77120257 | ||||||
| chr13:77120287
|
G | A | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.8140+1086C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77120287 | ||||||
| chr13:77120293
|
A | G | 1 | a0001c0002t0002g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.8140+1080T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77120293 | ||||||
| chr13:77120310
|
G | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.8140+1063C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77120310 | ||||||
| chr13:77120372
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.8140+1001G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77120372 | ||||||
| chr13:77120907
|
G | A | 1 | a0001c0003t0001g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8140+466C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77120907 | ||||||
| chr13:77121083
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.8140+290C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77121083 | ||||||
| chr13:77121139
|
A | T | 14 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(11): Show | 14 | HG00438.hp2 HG01255.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.8140+234T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77121139 | ||||||
| chr13:77121162
|
C | T | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.8140+211G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77121162 | ||||||
| chr13:77121258
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.8140+115G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 55/82 | chr13 | 77121258 | ||||||
| chr13:77121839
|
G | T | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.8018-344C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77121839 | ||||||
| chr13:77121901
|
T | C | 1 | a0001c0001t0001g0304 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.8018-406A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77121901 | ||||||
| chr13:77122010
|
CATAAAG | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.8018-521_8018-516d others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122010 | ||||||
| chr13:77122121
|
C | T | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.8018-626G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122121 | ||||||
| chr13:77122352
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.8018-857A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122352 | ||||||
| chr13:77122428
|
G | A | 17 | a0001c0004t0001g0087a0001c0004t0001g0150a0001c0004t0001g0153others(14): Show | 17 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.8018-933C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122428 | ||||||
| chr13:77122476
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.8018-981G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122476 | ||||||
| chr13:77122545
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.8018-1050G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122545 | ||||||
| chr13:77122562
|
G | A | 1 | a0001c0006t0001g0333 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8018-1067C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122562 | ||||||
| chr13:77122607
|
A | G | 20 | a0001c0003t0001g0031a0001c0003t0001g0129a0001c0008t0001g0263others(17): Show | 20 | HG00621.hp1 HG00735.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.8018-1112T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122607 | ||||||
| chr13:77122639
|
G | A | 2 | a0001c0002t0001g0069a0001c0029t0001g0065 | 2 | HG01515.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.8018-1144C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122639 | ||||||
| chr13:77122689
|
C | CA | 15 | a0001c0003t0001g0016a0001c0003t0001g0031a0001c0004t0001g0303others(12): Show | 15 | HG00642.hp1 HG00735.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.8018-1195dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122689 | ||||||
| chr13:77122689
|
C | CAA | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02055.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.8018-1196_8018-119 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122689 | ||||||
| chr13:77122689
|
CA | C | 7 | a0001c0001t0001g0290a0001c0001t0003g0005a0001c0006t0001g0319others(4): Show | 7 | HG00544.hp1 HG01168.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.8018-1195delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77122689 | ||||||
| chr13:77123252
|
G | C | 1 | a0002c0040t0001g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.8018-1757C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77123252 | ||||||
| chr13:77123379
|
A | C | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(150): Show | 153 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.8018-1884T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77123379 | ||||||
| chr13:77123619
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.8017+1717A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77123619 | ||||||
| chr13:77123626
|
T | C | 1 | a0001c0003t0001g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.8017+1710A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77123626 | ||||||
| chr13:77123633
|
G | A | 1 | a0001c0003t0001g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8017+1703C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77123633 | ||||||
| chr13:77123660
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.8017+1676G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77123660 | ||||||
| chr13:77123901
|
A | G | 3 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0203 | 3 | HG02027.hp1 NA18947.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.8017+1435T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77123901 | ||||||
| chr13:77124185
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0247 | 2 | HG00597.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.8017+1151G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77124185 | ||||||
| chr13:77124374
|
G | C | 1 | a0001c0044t0001g0332 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.8017+962C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77124374 | ||||||
| chr13:77124544
|
T | C | 1 | a0010c0025t0001g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.8017+792A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77124544 | ||||||
| chr13:77124545
|
G | T | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.8017+791C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77124545 | ||||||
| chr13:77124559
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.8017+777A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77124559 | ||||||
| chr13:77124668
|
A | G | 95 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(92): Show | 95 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.8017+668T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77124668 | ||||||
| chr13:77124669
|
T | C | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.8017+667A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77124669 | ||||||
| chr13:77124689
|
A | G | 2 | a0001c0003t0001g0022a0001c0003t0001g0023 | 2 | HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.8017+647T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77124689 | ||||||
| chr13:77124800
|
AAG | A | 16 | a0001c0006t0001g0317a0001c0006t0001g0318a0001c0006t0001g0319others(13): Show | 16 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.8017+534_8017+535d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77124800 | ||||||
| chr13:77124928
|
T | C | 153 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(150): Show | 153 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.8017+408A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77124928 | ||||||
| chr13:77125127
|
T | A | 4 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.8017+209A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 54/82 | chr13 | 77125127 | ||||||
| chr13:77125573
|
T | A | 1 | a0001c0020t0001g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.7885-105A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 53/82 | chr13 | 77125573 | ||||||
| chr13:77125583
|
C | G | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.7885-115G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 53/82 | chr13 | 77125583 | ||||||
| chr13:77125740
|
C | T | 1 | a0001c0003t0001g0072 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.7885-272G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 53/82 | chr13 | 77125740 | ||||||
| chr13:77125766
|
A | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7885-298T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 53/82 | chr13 | 77125766 | ||||||
| chr13:77126656
|
A | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.7660-114T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77126656 | ||||||
| chr13:77126774
|
A | G | 50 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(47): Show | 50 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.7660-232T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77126774 | ||||||
| chr13:77126940
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.7660-398C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77126940 | ||||||
| chr13:77127149
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7660-607A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77127149 | ||||||
| chr13:77127260
|
T | A | 1 | a0001c0002t0001g0026 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.7660-718A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77127260 | ||||||
| chr13:77127478
|
T | G | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.7660-936A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77127478 | ||||||
| chr13:77127579
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.7660-1037G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77127579 | ||||||
| chr13:77127662
|
G | A | 326 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.7660-1120C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77127662 | ||||||
| chr13:77127805
|
C | T | 3 | a0001c0004t0001g0087a0001c0004t0001g0244a0001c0004t0001g0279 | 3 | HG00621.hp2 NA18984.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.7660-1263G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77127805 | ||||||
| chr13:77127841
|
G | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7660-1299C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77127841 | ||||||
| chr13:77128011
|
C | A | 1 | a0001c0021t0001g0301 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7660-1469G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77128011 | ||||||
| chr13:77128108
|
A | G | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.7660-1566T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77128108 | ||||||
| chr13:77128130
|
C | T | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.7660-1588G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77128130 | ||||||
| chr13:77128572
|
A | G | 1 | a0016c0028t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7660-2030T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77128572 | ||||||
| chr13:77128600
|
A | G | 1 | a0001c0006t0001g0333 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.7660-2058T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77128600 | ||||||
| chr13:77128627
|
AG | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7660-2086delC | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77128627 | ||||||
| chr13:77128652
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.7660-2110C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77128652 | ||||||
| chr13:77129090
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.7660-2548G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77129090 | ||||||
| chr13:77129104
|
T | C | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.7660-2562A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77129104 | ||||||
| chr13:77129301
|
C | T | 1 | a0001c0005t0002g0131 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.7660-2759G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77129301 | ||||||
| chr13:77129328
|
C | T | 6 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0305others(3): Show | 6 | HG02109.hp2 HG02818.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.7660-2786G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77129328 | ||||||
| chr13:77129548
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7660-3006A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77129548 | ||||||
| chr13:77129550
|
T | C | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.7660-3008A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77129550 | ||||||
| chr13:77129751
|
A | G | 1 | a0001c0001t0001g0313 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.7660-3209T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77129751 | ||||||
| chr13:77129769
|
T | C | 1 | a0001c0006t0001g0318 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.7660-3227A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77129769 | ||||||
| chr13:77129813
|
T | A | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.7660-3271A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77129813 | ||||||
| chr13:77130038
|
C | T | 1 | a0001c0003t0001g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.7660-3496G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130038 | ||||||
| chr13:77130089
|
T | C | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.7660-3547A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130089 | ||||||
| chr13:77130099
|
C | G | 1 | a0001c0003t0001g0071 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7660-3557G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130099 | ||||||
| chr13:77130148
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0294 | 2 | HG00280.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.7660-3606G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130148 | ||||||
| chr13:77130183
|
C | T | 71 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(68): Show | 71 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.7660-3641G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130183 | ||||||
| chr13:77130285
|
GTCATTTT others(25): Show |
G | 1 | a0001c0006t0001g0333 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.7660-3775_7660-374 others(36): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130285 | ||||||
| chr13:77130311
|
CATT | C | 4 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(1): Show | 4 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7660-3772_7660-377 others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130311 | ||||||
| chr13:77130388
|
T | A | 2 | a0001c0008t0001g0302a0001c0008t0001g0306 | 2 | HG00735.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.7660-3846A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130388 | ||||||
| chr13:77130430
|
T | C | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.7660-3888A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130430 | ||||||
| chr13:77130441
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7660-3899T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130441 | ||||||
| chr13:77130468
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7660-3926G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130468 | ||||||
| chr13:77130676
|
A | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7660-4134T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130676 | ||||||
| chr13:77130692
|
G | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7660-4150C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130692 | ||||||
| chr13:77130729
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.7660-4187A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130729 | ||||||
| chr13:77130998
|
T | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.7660-4456A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77130998 | ||||||
| chr13:77131388
|
A | G | 1 | a0011c0024t0001g0092 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.7660-4846T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131388 | ||||||
| chr13:77131487
|
A | AAC | 7 | a0001c0001t0001g0141a0001c0004t0001g0151a0001c0006t0001g0323others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.7660-4947_7660-494 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131487 | ||||||
| chr13:77131487
|
A | AACAC | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.7660-4949_7660-494 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131487 | ||||||
| chr13:77131505
|
C | T | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.7660-4963G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131505 | ||||||
| chr13:77131507
|
CACACAAA others(3): Show |
C | 1 | a0001c0005t0002g0136 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.7660-4975_7660-496 others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131507 | ||||||
| chr13:77131509
|
C | CACACAA | 32 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(29): Show | 32 | HG01255.hp2 HG01257.hp1 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.7660-4968_7660-496 others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131509 | ||||||
| chr13:77131511
|
C | A | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.7660-4969G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131511 | ||||||
| chr13:77131511
|
CAA | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.7660-4971_7660-497 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131511 | ||||||
| chr13:77131513
|
A | AACACAC | 7 | a0001c0003t0001g0015a0001c0003t0001g0017a0001c0003t0001g0019others(4): Show | 7 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.7660-4972_7660-497 others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131513 | ||||||
| chr13:77131513
|
A | C | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.7660-4971T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131513 | ||||||
| chr13:77131513
|
AACAAACA others(5): Show |
A | 20 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(17): Show | 20 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.7660-4983_7660-497 others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131513 | ||||||
| chr13:77131515
|
C | A | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.7660-4973G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131515 | ||||||
| chr13:77131517
|
A | AAC | 187 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0089others(184): Show | 188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.7660-4977_7660-497 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131517 | ||||||
| chr13:77131517
|
A | AACAC | 3 | a0001c0004t0001g0154a0001c0004t0001g0278a0001c0043t0001g0292 | 3 | HG00408.hp2 HG02080.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.7660-4979_7660-497 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131517 | ||||||
| chr13:77131517
|
A | C | 47 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(44): Show | 47 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.7660-4975T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131517 | ||||||
| chr13:77131517
|
AAC | A | 11 | a0001c0003t0001g0071a0001c0003t0001g0072a0001c0008t0001g0263others(8): Show | 11 | HG00735.hp2 HG02109.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.7660-4977_7660-497 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131517 | ||||||
| chr13:77131521
|
C | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.7660-4979G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131521 | ||||||
| chr13:77131525
|
C | A | 1 | a0001c0005t0002g0136 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.7660-4983G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131525 | ||||||
| chr13:77131557
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.7660-5015A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131557 | ||||||
| chr13:77131589
|
T | C | 2 | a0001c0008t0001g0302a0001c0008t0001g0306 | 2 | HG00735.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.7660-5047A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131589 | ||||||
| chr13:77131613
|
T | C | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.7660-5071A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131613 | ||||||
| chr13:77131614
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7660-5072A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131614 | ||||||
| chr13:77131724
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7660-5182A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131724 | ||||||
| chr13:77131728
|
T | C | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.7660-5186A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131728 | ||||||
| chr13:77131939
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.7660-5397A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77131939 | ||||||
| chr13:77132071
|
T | A | 2 | a0001c0002t0001g0119a0001c0002t0001g0149 | 2 | NA18955.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.7660-5529A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77132071 | ||||||
| chr13:77132223
|
C | T | 1 | a0001c0002t0001g0105 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.7660-5681G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77132223 | ||||||
| chr13:77132459
|
T | C | 326 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.7660-5917A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77132459 | ||||||
| chr13:77132645
|
AC | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.7660-6104delG | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77132645 | ||||||
| chr13:77132895
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 4 | NA18747.hp1 NA19000.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.7659+6301C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77132895 | ||||||
| chr13:77133156
|
T | C | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.7659+6040A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77133156 | ||||||
| chr13:77133342
|
T | C | 5 | a0001c0001t0001g0176a0001c0001t0001g0194a0001c0001t0001g0195others(2): Show | 5 | HG01109.hp2 HG01928.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.7659+5854A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77133342 | ||||||
| chr13:77133436
|
C | A | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.7659+5760G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77133436 | ||||||
| chr13:77133745
|
A | G | 1 | a0001c0002t0001g0055 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.7659+5451T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77133745 | ||||||
| chr13:77133818
|
T | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.7659+5378A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77133818 | ||||||
| chr13:77134284
|
C | T | 14 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(11): Show | 14 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.7659+4912G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77134284 | ||||||
| chr13:77134305
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7659+4891C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77134305 | ||||||
| chr13:77134489
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.7659+4707C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77134489 | ||||||
| chr13:77134544
|
C | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7659+4652G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77134544 | ||||||
| chr13:77134582
|
C | CA | 30 | a0001c0003t0001g0031a0001c0005t0002g0078a0001c0005t0002g0079others(27): Show | 30 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.7659+4613dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77134582 | ||||||
| chr13:77134888
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.7659+4308G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77134888 | ||||||
| chr13:77135129
|
T | G | 1 | a0001c0003t0001g0014 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7659+4067A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135129 | ||||||
| chr13:77135152
|
C | T | 12 | a0001c0003t0001g0014a0001c0003t0001g0028a0001c0003t0001g0029others(9): Show | 12 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.7659+4044G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135152 | ||||||
| chr13:77135159
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.7659+4037G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135159 | ||||||
| chr13:77135179
|
T | C | 110 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(107): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.7659+4017A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135179 | ||||||
| chr13:77135306
|
C | T | 1 | a0001c0002t0001g0059 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.7659+3890G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135306 | ||||||
| chr13:77135323
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.7659+3873C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135323 | ||||||
| chr13:77135406
|
T | C | 1 | a0001c0002t0001g0056 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.7659+3790A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135406 | ||||||
| chr13:77135546
|
C | T | 1 | a0014c0032t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7659+3650G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135546 | ||||||
| chr13:77135635
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7659+3561T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135635 | ||||||
| chr13:77135840
|
T | A | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.7659+3356A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135840 | ||||||
| chr13:77135859
|
C | T | 1 | a0001c0009t0001g0310 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.7659+3337G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135859 | ||||||
| chr13:77135968
|
T | G | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.7659+3228A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77135968 | ||||||
| chr13:77136059
|
T | C | 4 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.7659+3137A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77136059 | ||||||
| chr13:77136067
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7659+3129A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77136067 | ||||||
| chr13:77136208
|
T | C | 2 | a0001c0003t0001g0020a0001c0003t0001g0021 | 2 | HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.7659+2988A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77136208 | ||||||
| chr13:77136236
|
C | T | 1 | a0001c0003t0001g0210 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.7659+2960G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77136236 | ||||||
| chr13:77136366
|
A | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7659+2830T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77136366 | ||||||
| chr13:77136720
|
T | C | 1 | a0001c0004t0001g0153 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.7659+2476A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77136720 | ||||||
| chr13:77136786
|
G | A | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.7659+2410C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77136786 | ||||||
| chr13:77136865
|
T | G | 1 | a0001c0044t0001g0332 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.7659+2331A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77136865 | ||||||
| chr13:77137066
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7659+2130T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77137066 | ||||||
| chr13:77137135
|
C | T | 1 | a0001c0020t0001g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.7659+2061G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77137135 | ||||||
| chr13:77137163
|
T | C | 1 | a0001c0001t0001g0007 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.7659+2033A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77137163 | ||||||
| chr13:77137449
|
T | G | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.7659+1747A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77137449 | ||||||
| chr13:77137532
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7659+1664G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77137532 | ||||||
| chr13:77137715
|
A | G | 2 | a0001c0003t0001g0260a0001c0003t0001g0261 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.7659+1481T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77137715 | ||||||
| chr13:77137887
|
C | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.7659+1309G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77137887 | ||||||
| chr13:77137924
|
C | A | 1 | a0001c0001t0001g0010 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7659+1272G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77137924 | ||||||
| chr13:77138139
|
G | A | 6 | a0001c0002t0001g0052a0001c0002t0001g0054a0001c0002t0001g0055others(3): Show | 6 | HG00609.hp2 HG02155.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.7659+1057C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77138139 | ||||||
| chr13:77138198
|
G | C | 29 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(26): Show | 29 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.7659+998C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77138198 | ||||||
| chr13:77138575
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.7659+621C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77138575 | ||||||
| chr13:77138626
|
G | C | 1 | a0001c0003t0001g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.7659+570C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77138626 | ||||||
| chr13:77138704
|
C | A | 88 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(85): Show | 89 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.7659+492G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77138704 | ||||||
| chr13:77138741
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.7659+455C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77138741 | ||||||
| chr13:77138764
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.7659+432C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 52/82 | chr13 | 77138764 | ||||||
| chr13:77139620
|
T | C | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.7519-284A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 51/82 | chr13 | 77139620 | ||||||
| chr13:77139751
|
C | A | 1 | a0001c0004t0001g0287 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7518+296G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 51/82 | chr13 | 77139751 | ||||||
| chr13:77139770
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7518+277C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 51/82 | chr13 | 77139770 | ||||||
| chr13:77139821
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(70): Show | 73 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.7518+226C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 51/82 | chr13 | 77139821 | ||||||
| chr13:77139859
|
C | T | 220 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(217): Show | 221 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.7518+188G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 51/82 | chr13 | 77139859 | ||||||
| chr13:77139868
|
A | G | 1 | a0001c0003t0001g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.7518+179T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 51/82 | chr13 | 77139868 | ||||||
| chr13:77139869
|
T | C | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.7518+178A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 51/82 | chr13 | 77139869 | ||||||
| chr13:77139920
|
G | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7518+127C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 51/82 | chr13 | 77139920 | ||||||
| chr13:77140419
|
G | C | 1 | a0001c0003t0006g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.7402-256C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 50/82 | chr13 | 77140419 | ||||||
| chr13:77140443
|
C | A | 1 | a0001c0001t0003g0002 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.7402-280G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 50/82 | chr13 | 77140443 | ||||||
| chr13:77140444
|
C | G | 1 | a0001c0001t0003g0002 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.7402-281G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 50/82 | chr13 | 77140444 | ||||||
| chr13:77141067
|
T | G | 7 | a0001c0001t0001g0034a0001c0001t0001g0163a0001c0001t0001g0173others(4): Show | 7 | HG00738.hp1 HG01255.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.7304-124A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77141067 | ||||||
| chr13:77141262
|
T | C | 8 | a0001c0004t0001g0087a0001c0004t0001g0153a0001c0004t0001g0240others(5): Show | 8 | HG00621.hp2 NA18946.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.7304-319A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77141262 | ||||||
| chr13:77141474
|
G | A | 1 | a0001c0004t0001g0088 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7304-531C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77141474 | ||||||
| chr13:77141588
|
T | C | 1 | a0006c0017t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.7304-645A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77141588 | ||||||
| chr13:77141598
|
C | T | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.7304-655G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77141598 | ||||||
| chr13:77141726
|
G | A | 110 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(107): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.7304-783C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77141726 | ||||||
| chr13:77141770
|
C | CA | 16 | a0001c0001t0001g0146a0001c0001t0001g0239a0001c0003t0001g0028others(13): Show | 16 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.7304-828dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77141770 | ||||||
| chr13:77141770
|
CA | C | 90 | a0001c0001t0001g0095a0001c0001t0001g0255a0001c0001t0003g0002others(87): Show | 91 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.7304-828delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77141770 | ||||||
| chr13:77142083
|
A | T | 1 | a0001c0005t0002g0222 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.7304-1140T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142083 | ||||||
| chr13:77142149
|
T | C | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.7304-1206A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142149 | ||||||
| chr13:77142210
|
C | G | 3 | a0001c0005t0002g0221a0001c0005t0002g0272a0001c0005t0002g0273 | 3 | HG01928.hp1 HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.7304-1267G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142210 | ||||||
| chr13:77142270
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0256 | 2 | NA18963.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.7304-1327T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142270 | ||||||
| chr13:77142334
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.7304-1391A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142334 | ||||||
| chr13:77142448
|
G | A | 5 | a0001c0005t0002g0222a0001c0005t0002g0224a0001c0005t0002g0268others(2): Show | 5 | NA18952.hp1 NA18982.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.7304-1505C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142448 | ||||||
| chr13:77142499
|
T | C | 1 | a0016c0028t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7304-1556A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142499 | ||||||
| chr13:77142575
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0189 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.7304-1632G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142575 | ||||||
| chr13:77142629
|
T | C | 1 | a0001c0001t0001g0314 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.7304-1686A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142629 | ||||||
| chr13:77142744
|
A | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.7303+1701T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142744 | ||||||
| chr13:77142906
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7303+1539A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142906 | ||||||
| chr13:77142907
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7303+1538G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142907 | ||||||
| chr13:77142919
|
A | C | 4 | a0001c0002t0001g0056a0001c0002t0001g0057a0001c0002t0001g0062others(1): Show | 4 | HG00423.hp1 NA18978.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.7303+1526T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77142919 | ||||||
| chr13:77143004
|
C | T | 208 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.7303+1441G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77143004 | ||||||
| chr13:77143232
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7303+1213C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77143232 | ||||||
| chr13:77143289
|
G | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.7303+1156C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77143289 | ||||||
| chr13:77143316
|
G | A | 1 | a0002c0007t0001g0215 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7303+1129C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77143316 | ||||||
| chr13:77143427
|
A | C | 1 | a0001c0002t0001g0257 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.7303+1018T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77143427 | ||||||
| chr13:77143474
|
C | T | 1 | a0001c0004t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.7303+971G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77143474 | ||||||
| chr13:77143538
|
A | G | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.7303+907T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77143538 | ||||||
| chr13:77143959
|
T | C | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.7303+486A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77143959 | ||||||
| chr13:77144205
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.7303+240T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77144205 | ||||||
| chr13:77144240
|
A | C | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.7303+205T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77144240 | ||||||
| chr13:77144251
|
G | A | 2 | a0001c0004t0001g0293a0001c0004t0001g0303 | 2 | HG01952.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.7303+194C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77144251 | ||||||
| chr13:77144285
|
TAATTA | T | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.7303+155_7303+159d others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77144285 | ||||||
| chr13:77144291
|
A | C | 11 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(8): Show | 11 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.7303+154T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77144291 | ||||||
| chr13:77144416
|
G | A | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.7303+29C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77144416 | ||||||
| chr13:77144417
|
T | C | 4 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(1): Show | 4 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.7303+28A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 49/82 | chr13 | 77144417 | ||||||
| chr13:77144681
|
C | A | 1 | a0001c0003t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.7188-121G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 48/82 | chr13 | 77144681 | ||||||
| chr13:77144826
|
A | T | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.7188-266T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 48/82 | chr13 | 77144826 | ||||||
| chr13:77144916
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0162 | 2 | HG01106.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.7188-356G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 48/82 | chr13 | 77144916 | ||||||
| chr13:77145016
|
T | C | 2 | a0001c0001t0001g0286a0001c0001t0001g0300 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.7188-456A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 48/82 | chr13 | 77145016 | ||||||
| chr13:77145210
|
C | T | 30 | a0001c0003t0001g0031a0001c0005t0002g0078a0001c0005t0002g0079others(27): Show | 30 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.7188-650G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 48/82 | chr13 | 77145210 | ||||||
| chr13:77145385
|
T | C | 39 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(36): Show | 39 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.7187+777A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 48/82 | chr13 | 77145385 | ||||||
| chr13:77145621
|
G | A | 1 | a0001c0004t0001g0244 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.7187+541C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 48/82 | chr13 | 77145621 | ||||||
| chr13:77146024
|
A | G | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.7187+138T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 48/82 | chr13 | 77146024 | ||||||
| chr13:77146457
|
T | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.7132-240A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77146457 | ||||||
| chr13:77146461
|
G | T | 2 | a0001c0002t0001g0119a0001c0002t0001g0149 | 2 | NA18955.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.7132-244C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77146461 | ||||||
| chr13:77146547
|
G | A | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.7132-330C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77146547 | ||||||
| chr13:77146582
|
A | G | 4 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.7132-365T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77146582 | ||||||
| chr13:77146592
|
T | C | 1 | a0001c0004t0001g0287 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.7132-375A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77146592 | ||||||
| chr13:77146643
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.7132-426G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77146643 | ||||||
| chr13:77146956
|
T | G | 1 | a0001c0003t0001g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7132-739A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77146956 | ||||||
| chr13:77147013
|
A | G | 110 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(107): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.7132-796T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77147013 | ||||||
| chr13:77147026
|
T | G | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.7132-809A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77147026 | ||||||
| chr13:77147065
|
G | A | 1 | a0001c0002t0001g0055 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.7132-848C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77147065 | ||||||
| chr13:77147295
|
G | T | 322 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.7132-1078C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77147295 | ||||||
| chr13:77147341
|
A | T | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.7132-1124T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77147341 | ||||||
| chr13:77147502
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0283 | 2 | NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.7132-1285A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77147502 | ||||||
| chr13:77147678
|
A | C | 1 | a0001c0001t0001g0247 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.7132-1461T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77147678 | ||||||
| chr13:77148033
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7132-1816T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77148033 | ||||||
| chr13:77148205
|
C | T | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01928.hp2 HG01934.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.7132-1988G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77148205 | ||||||
| chr13:77148219
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.7132-2002C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77148219 | ||||||
| chr13:77148382
|
G | T | 1 | a0001c0002t0001g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.7132-2165C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77148382 | ||||||
| chr13:77148440
|
C | A | 4 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(1): Show | 4 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.7132-2223G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77148440 | ||||||
| chr13:77148510
|
A | ACT | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.7131+2222_7131+222 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77148510 | ||||||
| chr13:77149069
|
A | G | 4 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.7131+1665T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77149069 | ||||||
| chr13:77149153
|
G | T | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.7131+1581C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77149153 | ||||||
| chr13:77149229
|
C | T | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.7131+1505G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77149229 | ||||||
| chr13:77149275
|
G | A | 210 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.7131+1459C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77149275 | ||||||
| chr13:77149316
|
A | G | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.7131+1418T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77149316 | ||||||
| chr13:77149426
|
G | A | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.7131+1308C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77149426 | ||||||
| chr13:77149539
|
T | C | 2 | a0001c0009t0001g0077a0001c0009t0001g0127 | 2 | HG02523.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.7131+1195A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77149539 | ||||||
| chr13:77149958
|
C | T | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.7131+776G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77149958 | ||||||
| chr13:77150139
|
G | A | 1 | a0001c0004t0001g0242 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.7131+595C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77150139 | ||||||
| chr13:77150169
|
A | G | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.7131+565T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77150169 | ||||||
| chr13:77150334
|
G | A | 1 | a0001c0003t0001g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7131+400C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77150334 | ||||||
| chr13:77150399
|
C | T | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.7131+335G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77150399 | ||||||
| chr13:77150412
|
G | T | 1 | a0001c0002t0001g0026 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.7131+322C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77150412 | ||||||
| chr13:77150443
|
G | A | 202 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.7131+291C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77150443 | ||||||
| chr13:77150621
|
C | CTTG | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.7131+112_7131+113i others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77150621 | ||||||
| chr13:77150629
|
G | T | 1 | a0001c0002t0001g0125 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.7131+105C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77150629 | ||||||
| chr13:77150689
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.7131+45G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77150689 | ||||||
| chr13:77150693
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.7131+41A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 47/82 | chr13 | 77150693 | ||||||
| chr13:77150971
|
C | A | 110 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(107): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.6916-22G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77150971 | ||||||
| chr13:77150983
|
ATTAT | A | 3 | a0001c0003t0001g0207a0001c0003t0006g0209a0001c0006t0001g0319 | 3 | HG02895.hp1 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.6916-38_6916-35del others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77150983 | ||||||
| chr13:77151163
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.6916-214G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77151163 | ||||||
| chr13:77151446
|
C | G | 1 | a0001c0009t0001g0128 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.6916-497G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77151446 | ||||||
| chr13:77151627
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.6916-678G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77151627 | ||||||
| chr13:77151676
|
C | G | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.6916-727G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77151676 | ||||||
| chr13:77151807
|
T | C | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.6916-858A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77151807 | ||||||
| chr13:77151921
|
C | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0252 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.6916-972G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77151921 | ||||||
| chr13:77151924
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.6916-975G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77151924 | ||||||
| chr13:77152128
|
C | T | 4 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(1): Show | 4 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.6916-1179G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152128 | ||||||
| chr13:77152383
|
A | G | 1 | a0001c0033t0001g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.6916-1434T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152383 | ||||||
| chr13:77152467
|
T | G | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6916-1518A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152467 | ||||||
| chr13:77152523
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6916-1574G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152523 | ||||||
| chr13:77152763
|
C | T | 2 | a0001c0003t0001g0041a0001c0003t0001g0042 | 2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.6916-1814G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152763 | ||||||
| chr13:77152824
|
T | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6916-1875A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152824 | ||||||
| chr13:77152851
|
G | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.6916-1902C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152851 | ||||||
| chr13:77152933
|
C | T | 1 | a0001c0002t0001g0171 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.6916-1984G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152933 | ||||||
| chr13:77152958
|
G | A | 1 | a0001c0003t0001g0210 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6916-2009C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152958 | ||||||
| chr13:77152983
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6916-2034A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152983 | ||||||
| chr13:77152988
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.6916-2039G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152988 | ||||||
| chr13:77152996
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.6916-2047G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77152996 | ||||||
| chr13:77153019
|
C | A | 1 | a0001c0002t0001g0059 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.6916-2070G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153019 | ||||||
| chr13:77153064
|
C | CA | 33 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0145others(30): Show | 33 | HG00423.hp1 HG00438.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.6916-2116dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153064 | ||||||
| chr13:77153064
|
CA | C | 96 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0034others(93): Show | 96 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.6916-2116delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153064 | ||||||
| chr13:77153064
|
CAA | C | 30 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(27): Show | 30 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.6916-2117_6916-211 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153064 | ||||||
| chr13:77153230
|
A | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(72): Show | 75 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.6916-2281T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153230 | ||||||
| chr13:77153315
|
T | C | 208 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.6916-2366A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153315 | ||||||
| chr13:77153560
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.6915+2498A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153560 | ||||||
| chr13:77153671
|
T | C | 1 | a0001c0008t0001g0307 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6915+2387A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153671 | ||||||
| chr13:77153697
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6915+2361A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153697 | ||||||
| chr13:77153705
|
CCTATGTG others(5): Show |
C | 14 | a0001c0006t0001g0317a0001c0006t0001g0318a0001c0006t0001g0319others(11): Show | 14 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.6915+2341_6915+235 others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153705 | ||||||
| chr13:77153717
|
T | C | 2 | a0001c0006t0001g0322a0001c0006t0001g0328 | 2 | HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.6915+2341A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153717 | ||||||
| chr13:77153752
|
C | CT | 327 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.6915+2305dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153752 | ||||||
| chr13:77153769
|
C | G | 15 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(12): Show | 15 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.6915+2289G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77153769 | ||||||
| chr13:77154063
|
C | A | 6 | a0001c0002t0001g0117a0001c0002t0001g0125a0001c0002t0001g0202others(3): Show | 6 | NA18953.hp1 NA18960.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.6915+1995G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77154063 | ||||||
| chr13:77154173
|
A | G | 5 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0249others(2): Show | 5 | HG00738.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.6915+1885T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77154173 | ||||||
| chr13:77154220
|
T | C | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.6915+1838A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77154220 | ||||||
| chr13:77154261
|
G | A | 3 | a0001c0004t0001g0265a0001c0004t0001g0266a0001c0004t0001g0267 | 3 | HG01071.hp2 HG01261.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.6915+1797C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77154261 | ||||||
| chr13:77154322
|
T | C | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.6915+1736A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77154322 | ||||||
| chr13:77154416
|
G | GA | 20 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(17): Show | 20 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.6915+1641dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77154416 | ||||||
| chr13:77154417
|
A | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.6915+1641T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77154417 | ||||||
| chr13:77154457
|
T | G | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.6915+1601A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77154457 | ||||||
| chr13:77154586
|
T | C | 39 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(36): Show | 39 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.6915+1472A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77154586 | ||||||
| chr13:77154614
|
T | G | 1 | a0001c0001t0001g0231 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.6915+1444A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77154614 | ||||||
| chr13:77154958
|
T | A | 38 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(35): Show | 38 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(35): Show |
intron_variant | MODIFIER | c.6915+1100A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77154958 | ||||||
| chr13:77155032
|
T | C | 17 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(14): Show | 17 | HG00735.hp2 HG02109.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.6915+1026A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77155032 | ||||||
| chr13:77155156
|
T | C | 6 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(3): Show | 6 | HG01928.hp2 HG01934.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.6915+902A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77155156 | ||||||
| chr13:77155194
|
T | A | 1 | a0001c0002t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6915+864A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77155194 | ||||||
| chr13:77155208
|
G | C | 1 | a0001c0001t0001g0313 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6915+850C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77155208 | ||||||
| chr13:77155551
|
A | G | 1 | a0001c0003t0001g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6915+507T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77155551 | ||||||
| chr13:77155831
|
C | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.6915+227G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77155831 | ||||||
| chr13:77155859
|
A | G | 4 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(1): Show | 4 | NA18942.hp1 NA18957.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.6915+199T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77155859 | ||||||
| chr13:77155884
|
T | C | 1 | a0015c0027t0007g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.6915+174A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77155884 | ||||||
| chr13:77155977
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.6915+81G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 46/82 | chr13 | 77155977 | ||||||
| chr13:77156441
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0239 | 2 | HG01257.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.6771-239A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77156441 | ||||||
| chr13:77156583
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.6771-381G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77156583 | ||||||
| chr13:77156592
|
A | T | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.6771-390T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77156592 | ||||||
| chr13:77157112
|
G | A | 1 | a0001c0026t0001g0285 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.6770+825C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77157112 | ||||||
| chr13:77157165
|
G | A | 13 | a0001c0003t0001g0014a0001c0003t0001g0028a0001c0003t0001g0029others(10): Show | 13 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.6770+772C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77157165 | ||||||
| chr13:77157416
|
A | G | 45 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(42): Show | 45 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(42): Show |
intron_variant | MODIFIER | c.6770+521T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77157416 | ||||||
| chr13:77157418
|
T | G | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.6770+519A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77157418 | ||||||
| chr13:77157499
|
C | T | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.6770+438G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77157499 | ||||||
| chr13:77157566
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0239 | 2 | HG01257.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.6770+371C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77157566 | ||||||
| chr13:77157608
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.6770+329G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77157608 | ||||||
| chr13:77157772
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6770+165G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77157772 | ||||||
| chr13:77157811
|
C | T | 2 | a0001c0002t0001g0048a0001c0002t0001g0067 | 2 | NA18979.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.6770+126G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77157811 | ||||||
| chr13:77157891
|
A | C | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.6770+46T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 45/82 | chr13 | 77157891 | ||||||
| chr13:77158198
|
G | A | 106 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(103): Show | 106 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.6598-89C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77158198 | ||||||
| chr13:77158205
|
C | T | 3 | a0001c0004t0001g0087a0001c0004t0001g0244a0001c0004t0001g0279 | 3 | HG00621.hp2 NA18984.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.6598-96G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77158205 | ||||||
| chr13:77158209
|
G | T | 1 | a0001c0002t0001g0149 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.6598-100C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77158209 | ||||||
| chr13:77159059
|
AT | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.6598-951delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77159059 | ||||||
| chr13:77159310
|
G | C | 1 | a0001c0002t0001g0105 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.6598-1201C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77159310 | ||||||
| chr13:77159613
|
T | G | 2 | a0001c0003t0001g0264a0001c0036t0001g0291 | 2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.6598-1504A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77159613 | ||||||
| chr13:77159623
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.6598-1514A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77159623 | ||||||
| chr13:77159732
|
G | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.6598-1623C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77159732 | ||||||
| chr13:77160065
|
C | CT | 85 | a0001c0001t0001g0082a0001c0001t0001g0233a0001c0002t0001g0001others(82): Show | 86 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.6597+1840dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77160065 | ||||||
| chr13:77160065
|
CT | C | 19 | a0001c0001t0001g0080a0001c0001t0001g0282a0001c0001t0004g0181others(16): Show | 19 | HG00735.hp2 HG00741.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.6597+1840delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77160065 | ||||||
| chr13:77160152
|
C | T | 1 | a0001c0002t0002g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6597+1754G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77160152 | ||||||
| chr13:77160272
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.6597+1634G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77160272 | ||||||
| chr13:77160302
|
A | G | 326 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.6597+1604T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77160302 | ||||||
| chr13:77160459
|
T | C | 1 | a0001c0026t0001g0285 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.6597+1447A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77160459 | ||||||
| chr13:77160553
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.6597+1353A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77160553 | ||||||
| chr13:77160629
|
G | A | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.6597+1277C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77160629 | ||||||
| chr13:77160692
|
T | C | 1 | a0001c0002t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6597+1214A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77160692 | ||||||
| chr13:77160841
|
C | A | 1 | a0001c0003t0001g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6597+1065G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77160841 | ||||||
| chr13:77161199
|
C | G | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.6597+707G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77161199 | ||||||
| chr13:77161290
|
C | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.6597+616G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77161290 | ||||||
| chr13:77161371
|
C | T | 1 | a0001c0045t0001g0327 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.6597+535G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77161371 | ||||||
| chr13:77161399
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.6597+507A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77161399 | ||||||
| chr13:77161403
|
A | C | 1 | a0001c0001t0001g0227 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.6597+503T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77161403 | ||||||
| chr13:77161404
|
A | G | 1 | a0001c0002t0002g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6597+502T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77161404 | ||||||
| chr13:77161576
|
C | T | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6597+330G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77161576 | ||||||
| chr13:77161652
|
G | A | 15 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(12): Show | 15 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.6597+254C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77161652 | ||||||
| chr13:77161820
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6597+86T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 44/82 | chr13 | 77161820 | ||||||
| chr13:77162016
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.6548-61A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77162016 | ||||||
| chr13:77162122
|
A | G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.6548-167T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77162122 | ||||||
| chr13:77162172
|
G | T | 1 | a0001c0002t0002g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6548-217C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77162172 | ||||||
| chr13:77162184
|
G | A | 110 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(107): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.6548-229C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77162184 | ||||||
| chr13:77162306
|
T | C | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.6548-351A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77162306 | ||||||
| chr13:77162591
|
T | C | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.6548-636A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77162591 | ||||||
| chr13:77162748
|
A | C | 39 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(36): Show | 39 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.6548-793T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77162748 | ||||||
| chr13:77162969
|
T | A | 1 | a0001c0002t0001g0257 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6548-1014A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77162969 | ||||||
| chr13:77162994
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.6548-1039G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77162994 | ||||||
| chr13:77163072
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6548-1117A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77163072 | ||||||
| chr13:77163072
|
T | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6548-1117A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77163072 | ||||||
| chr13:77163271
|
T | C | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.6547+1183A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77163271 | ||||||
| chr13:77163336
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6547+1118A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77163336 | ||||||
| chr13:77163493
|
G | T | 4 | a0001c0006t0001g0317a0001c0006t0001g0318a0001c0006t0001g0330others(1): Show | 4 | HG00642.hp2 HG01069.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.6547+961C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77163493 | ||||||
| chr13:77164011
|
G | C | 203 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.6547+443C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77164011 | ||||||
| chr13:77164229
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6547+225A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77164229 | ||||||
| chr13:77164431
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.6547+23G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77164431 | ||||||
| chr13:77164432
|
A | T | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.6547+22T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 43/82 | chr13 | 77164432 | ||||||
| chr13:77164718
|
T | C | 1 | a0001c0005t0002g0272 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.6460-177A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 42/82 | chr13 | 77164718 | ||||||
| chr13:77164783
|
G | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.6460-242C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 42/82 | chr13 | 77164783 | ||||||
| chr13:77165156
|
A | T | 210 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.6459+117T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 42/82 | chr13 | 77165156 | ||||||
| chr13:77165159
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.6459+114G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 42/82 | chr13 | 77165159 | ||||||
| chr13:77165170
|
C | T | 3 | a0001c0001t0001g0282a0001c0001t0001g0294a0001c0036t0001g0291 | 3 | HG00280.hp2 HG02055.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.6459+103G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 42/82 | chr13 | 77165170 | ||||||
| chr13:77165526
|
G | A | 87 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(84): Show | 88 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.6341-135C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 41/82 | chr13 | 77165526 | ||||||
| chr13:77165532
|
C | T | 39 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(36): Show | 39 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.6341-141G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 41/82 | chr13 | 77165532 | ||||||
| chr13:77166238
|
A | C | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.6340+91T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 41/82 | chr13 | 77166238 | ||||||
| chr13:77166313
|
GA | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.6340+15delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 41/82 | chr13 | 77166313 | ||||||
| chr13:77166562
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.6115-8G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166562 | ||||||
| chr13:77166574
|
T | C | 50 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(47): Show | 50 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.6115-20A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166574 | ||||||
| chr13:77166674
|
C | A | 1 | a0001c0008t0001g0302 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.6115-120G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166674 | ||||||
| chr13:77166966
|
A | AATACACA others(5): Show |
1 | a0001c0003t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6115-413_6115-412i others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166966 | ||||||
| chr13:77166966
|
AACACACA others(3): Show |
A | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG00099.hp1 NA18946.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.6115-422_6115-413d others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166966 | ||||||
| chr13:77166966
|
AACACACA others(7): Show |
A | 7 | a0001c0005t0002g0222a0001c0005t0002g0223a0001c0005t0002g0224others(4): Show | 7 | NA18952.hp1 NA18982.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.6115-426_6115-413d others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166966 | ||||||
| chr13:77166968
|
C | T | 13 | a0001c0003t0001g0041a0001c0003t0001g0042a0001c0003t0001g0073others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.6115-414G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166968 | ||||||
| chr13:77166968
|
CACACACA others(1): Show |
C | 6 | a0001c0001t0001g0282a0001c0001t0001g0294a0001c0005t0002g0221others(3): Show | 6 | HG00280.hp2 HG01496.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.6115-422_6115-415d others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166968 | ||||||
| chr13:77166970
|
CACACAT | C | 3 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0137 | 3 | NA18966.hp2 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.6115-422_6115-417d others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166970 | ||||||
| chr13:77166976
|
T | C | 1 | a0001c0003t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.6115-422A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166976 | ||||||
| chr13:77166976
|
T | TAC | 7 | a0001c0003t0001g0041a0001c0003t0006g0209a0001c0016t0001g0006others(4): Show | 7 | HG01099.hp1 HG02486.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.6115-424_6115-423d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166976 | ||||||
| chr13:77166976
|
T | TACAC | 3 | a0001c0003t0001g0207a0001c0003t0001g0264a0001c0003t0001g0289 | 3 | HG02004.hp2 HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.6115-426_6115-423d others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166976 | ||||||
| chr13:77166976
|
TAC | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(10): Show | 13 | HG01256.hp2 HG01258.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.6115-424_6115-423d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166976 | ||||||
| chr13:77166976
|
TACAC | T | 81 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(78): Show | 81 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.6115-426_6115-423d others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166976 | ||||||
| chr13:77166976
|
TACACAC | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0160others(51): Show | 54 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.6115-428_6115-423d others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166976 | ||||||
| chr13:77166976
|
TACACACA others(1): Show |
T | 113 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0089others(110): Show | 114 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.6115-430_6115-423d others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166976 | ||||||
| chr13:77166976
|
TACACACA others(3): Show |
T | 10 | a0001c0001t0001g0172a0001c0002t0001g0066a0001c0003t0001g0016others(7): Show | 10 | HG00735.hp2 HG02523.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.6115-432_6115-423d others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166976 | ||||||
| chr13:77166976
|
TACACACA others(5): Show |
T | 8 | a0001c0002t0001g0100a0001c0003t0001g0031a0001c0008t0001g0263others(5): Show | 8 | HG02109.hp2 HG02145.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.6115-434_6115-423d others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166976 | ||||||
| chr13:77166976
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6115-436_6115-423d others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166976 | ||||||
| chr13:77166978
|
C | T | 3 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0137 | 3 | NA18966.hp2 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.6115-424G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166978 | ||||||
| chr13:77166980
|
C | T | 4 | a0001c0005t0002g0221a0001c0005t0002g0272a0001c0005t0002g0273others(1): Show | 4 | HG01496.hp2 HG01928.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.6115-426G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166980 | ||||||
| chr13:77166982
|
C | T | 6 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(3): Show | 6 | HG00099.hp1 NA18946.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.6115-428G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166982 | ||||||
| chr13:77166986
|
C | T | 7 | a0001c0005t0002g0222a0001c0005t0002g0223a0001c0005t0002g0224others(4): Show | 7 | NA18952.hp1 NA18982.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.6115-432G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77166986 | ||||||
| chr13:77167019
|
ACACACAC | A | 3 | a0001c0001t0001g0190a0001c0002t0001g0054a0001c0002t0001g0062 | 3 | HG02155.hp1 NA18961.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.6115-472_6115-466d others(9): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77167019 | ||||||
| chr13:77167023
|
A | C | 25 | a0001c0001t0001g0235a0001c0005t0002g0078a0001c0005t0002g0079others(22): Show | 25 | HG00099.hp1 HG00621.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.6115-469T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77167023 | ||||||
| chr13:77167025
|
A | C | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 91 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.6115-471T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77167025 | ||||||
| chr13:77167026
|
C | T | 1 | a0001c0004t0001g0087 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.6115-472G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77167026 | ||||||
| chr13:77167708
|
T | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0294 | 2 | HG00280.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.6114+720A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77167708 | ||||||
| chr13:77167732
|
T | C | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.6114+696A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77167732 | ||||||
| chr13:77167956
|
C | T | 1 | a0001c0002t0001g0259 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.6114+472G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77167956 | ||||||
| chr13:77168194
|
G | A | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.6114+234C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77168194 | ||||||
| chr13:77168401
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.6114+27G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77168401 | ||||||
| chr13:77168402
|
G | A | 7 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.6114+26C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 40/82 | chr13 | 77168402 | ||||||
| chr13:77168654
|
A | C | 1 | a0001c0003t0001g0261 | 1 | HG01258.hp1 | splice_region_variant&intron_variant | LOW | c.5896-8T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77168654 | ||||||
| chr13:77168738
|
C | T | 1 | a0010c0025t0001g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5896-92G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77168738 | ||||||
| chr13:77168797
|
G | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0239 | 2 | HG01257.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.5896-151C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77168797 | ||||||
| chr13:77168800
|
TA | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.5896-155delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77168800 | ||||||
| chr13:77169138
|
G | A | 2 | a0001c0001t0004g0181a0001c0001t0004g0184 | 2 | NA18942.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.5895+476C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169138 | ||||||
| chr13:77169139
|
T | G | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.5895+475A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169139 | ||||||
| chr13:77169179
|
C | T | 86 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.5895+435G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169179 | ||||||
| chr13:77169191
|
G | A | 17 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(14): Show | 17 | HG00735.hp2 HG02109.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.5895+423C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169191 | ||||||
| chr13:77169213
|
G | A | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | NA18954.hp2 NA18964.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.5895+401C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169213 | ||||||
| chr13:77169224
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.5895+390C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169224 | ||||||
| chr13:77169252
|
C | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.5895+362G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169252 | ||||||
| chr13:77169312
|
C | T | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.5895+302G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169312 | ||||||
| chr13:77169313
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0294 | 2 | HG00280.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.5895+301C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169313 | ||||||
| chr13:77169321
|
G | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.5895+293C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169321 | ||||||
| chr13:77169327
|
C | T | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5895+287G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169327 | ||||||
| chr13:77169328
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5895+286C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169328 | ||||||
| chr13:77169347
|
G | T | 2 | a0001c0006t0001g0330a0001c0006t0001g0331 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.5895+267C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169347 | ||||||
| chr13:77169348
|
A | T | 2 | a0001c0006t0001g0330a0001c0006t0001g0331 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.5895+266T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169348 | ||||||
| chr13:77169390
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5895+224G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169390 | ||||||
| chr13:77169395
|
C | CA | 24 | a0001c0001t0001g0008a0001c0001t0001g0090a0001c0001t0001g0172others(21): Show | 24 | HG00423.hp1 HG01243.hp2 HG01952.hp2 others(21): Show |
intron_variant | MODIFIER | c.5895+218dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169395 | ||||||
| chr13:77169566
|
A | G | 1 | a0001c0002t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5895+48T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 39/82 | chr13 | 77169566 | ||||||
| chr13:77169752
|
G | A | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5795-38C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77169752 | ||||||
| chr13:77169770
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5795-56G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77169770 | ||||||
| chr13:77169813
|
G | A | 4 | a0001c0006t0001g0323a0001c0006t0001g0324a0001c0006t0001g0325others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.5795-99C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77169813 | ||||||
| chr13:77169886
|
C | A | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.5795-172G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77169886 | ||||||
| chr13:77169926
|
T | A | 1 | a0001c0002t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5795-212A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77169926 | ||||||
| chr13:77169966
|
T | C | 5 | a0001c0006t0001g0321a0001c0006t0001g0323a0001c0006t0001g0324others(2): Show | 5 | HG00733.hp2 HG00738.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.5795-252A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77169966 | ||||||
| chr13:77170178
|
G | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.5795-464C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77170178 | ||||||
| chr13:77170255
|
A | G | 1 | a0001c0008t0001g0308 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5795-541T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77170255 | ||||||
| chr13:77170522
|
C | T | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.5795-808G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77170522 | ||||||
| chr13:77170577
|
C | CT | 31 | a0001c0001t0001g0143a0001c0003t0001g0015a0001c0003t0001g0016others(28): Show | 31 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.5795-864dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77170577 | ||||||
| chr13:77170577
|
CT | C | 14 | a0001c0001t0001g0142a0001c0003t0001g0072a0001c0003t0001g0129others(11): Show | 14 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.5795-864delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77170577 | ||||||
| chr13:77170664
|
C | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5794+828G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77170664 | ||||||
| chr13:77170721
|
C | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.5794+771G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77170721 | ||||||
| chr13:77170822
|
T | G | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.5794+670A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77170822 | ||||||
| chr13:77170870
|
C | T | 2 | a0001c0006t0001g0328a0001c0006t0001g0329 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5794+622G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77170870 | ||||||
| chr13:77170969
|
C | T | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.5794+523G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77170969 | ||||||
| chr13:77171158
|
C | T | 1 | a0001c0045t0001g0327 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5794+334G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77171158 | ||||||
| chr13:77171413
|
C | A | 3 | a0001c0003t0001g0129a0001c0012t0001g0074a0001c0012t0001g0075 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.5794+79G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77171413 | ||||||
| chr13:77171448
|
A | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.5794+44T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 38/82 | chr13 | 77171448 | ||||||
| chr13:77171732
|
A | G | 1 | a0001c0002t0001g0103 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5652-98T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77171732 | ||||||
| chr13:77171776
|
A | T | 330 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.5652-142T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77171776 | ||||||
| chr13:77171935
|
C | A | 2 | a0001c0003t0001g0032a0001c0035t0001g0030 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.5652-301G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77171935 | ||||||
| chr13:77171939
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.5652-305G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77171939 | ||||||
| chr13:77171940
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5652-306C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77171940 | ||||||
| chr13:77172058
|
G | A | 3 | a0001c0004t0001g0088a0001c0004t0001g0151a0001c0004t0001g0174 | 3 | HG02258.hp1 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5652-424C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77172058 | ||||||
| chr13:77172191
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5652-557G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77172191 | ||||||
| chr13:77172205
|
AT | A | 6 | a0001c0001t0001g0141a0001c0003t0001g0028a0001c0004t0001g0265others(3): Show | 6 | HG01071.hp2 HG01975.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.5652-572delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77172205 | ||||||
| chr13:77172370
|
T | G | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5652-736A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77172370 | ||||||
| chr13:77172503
|
C | T | 4 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(1): Show | 4 | NA18942.hp1 NA18957.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.5652-869G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77172503 | ||||||
| chr13:77172507
|
T | C | 8 | a0002c0007t0001g0212a0002c0007t0001g0213a0002c0007t0001g0214others(5): Show | 8 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.5652-873A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77172507 | ||||||
| chr13:77172999
|
G | C | 1 | a0001c0002t0001g0149 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5651+1312C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77172999 | ||||||
| chr13:77173320
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5651+991G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77173320 | ||||||
| chr13:77173321
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5651+990C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77173321 | ||||||
| chr13:77173456
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5651+855C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77173456 | ||||||
| chr13:77173468
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5651+843A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77173468 | ||||||
| chr13:77173575
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0189 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.5651+736G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77173575 | ||||||
| chr13:77173770
|
C | G | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.5651+541G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77173770 | ||||||
| chr13:77173900
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5651+411G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77173900 | ||||||
| chr13:77174298
|
T | C | 1 | a0001c0004t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.5651+13A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 37/82 | chr13 | 77174298 | ||||||
| chr13:77174745
|
T | C | 4 | a0001c0002t0001g0149a0001c0004t0001g0154a0001c0004t0001g0278others(1): Show | 4 | HG00408.hp2 HG02080.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.5473-256A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174745 | ||||||
| chr13:77174786
|
A | G | 1 | a0001c0006t0001g0333 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5473-297T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174786 | ||||||
| chr13:77174812
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5473-323C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174812 | ||||||
| chr13:77174896
|
A | G | 2 | a0001c0003t0001g0032a0001c0035t0001g0030 | 2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.5473-407T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174896 | ||||||
| chr13:77174902
|
T | TATATATA others(165): Show |
2 | a0001c0003t0001g0018a0001c0003t0001g0019 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5473-414_5473-413i others(174): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174902 | ||||||
| chr13:77174902
|
T | TATATATA others(169): Show |
3 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017 | 3 | HG03098.hp2 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.5473-414_5473-413i others(178): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174902 | ||||||
| chr13:77174902
|
T | TATATATA others(169): Show |
1 | a0001c0003t0001g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5473-414_5473-413i others(178): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174902 | ||||||
| chr13:77174902
|
T | TATATATA others(171): Show |
1 | a0001c0003t0001g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5473-414_5473-413i others(180): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174902 | ||||||
| chr13:77174902
|
T | TATATATA others(167): Show |
2 | a0001c0003t0001g0020a0001c0003t0001g0021 | 2 | HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.5473-414_5473-413i others(176): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174902 | ||||||
| chr13:77174902
|
T | TATATATA others(83): Show |
3 | a0001c0003t0001g0129a0001c0012t0001g0074a0001c0012t0001g0075 | 3 | HG01069.hp2 HG01071.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.5473-414_5473-413i others(92): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174902 | ||||||
| chr13:77174902
|
T | TATATATA others(69): Show |
21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.5473-414_5473-413i others(78): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174902 | ||||||
| chr13:77174906
|
T | TATATAAT others(221): Show |
1 | a0001c0002t0001g0049 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.5473-418_5473-417i others(230): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174906 | ||||||
| chr13:77174910
|
T | TAATATAT others(28): Show |
117 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(114): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.5473-422_5473-421i others(37): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(135): Show |
3 | a0001c0002t0001g0048a0001c0002t0001g0059a0001c0002t0001g0067 | 3 | HG00558.hp1 NA18979.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.5473-422_5473-421i others(144): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(25): Show |
1 | a0001c0003t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(34): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(25): Show |
13 | a0001c0003t0001g0041a0001c0003t0001g0042a0001c0003t0001g0073others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.5473-422_5473-421i others(34): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(190): Show |
1 | a0001c0002t0001g0058 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(199): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(156): Show |
4 | a0001c0002t0001g0066a0001c0006t0001g0319a0001c0006t0001g0320others(1): Show | 4 | HG01891.hp2 HG03688.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.5473-422_5473-421i others(165): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(183): Show |
1 | a0001c0002t0001g0110 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(192): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(188): Show |
1 | a0001c0002t0001g0149 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(197): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(171): Show |
3 | a0001c0002t0001g0108a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | NA18986.hp1 NA19054.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.5473-422_5473-421i others(180): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(184): Show |
1 | a0014c0032t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(193): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(172): Show |
1 | a0001c0002t0001g0202 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(181): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(188): Show |
1 | a0001c0002t0001g0119 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(197): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(190): Show |
56 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0052others(53): Show | 57 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.5473-422_5473-421i others(199): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(181): Show |
2 | a0001c0006t0001g0330a0001c0006t0001g0331 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.5473-422_5473-421i others(190): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(188): Show |
2 | a0001c0006t0001g0317a0001c0006t0001g0318 | 2 | HG00642.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.5473-422_5473-421i others(197): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(190): Show |
1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(199): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(141): Show |
1 | a0001c0002t0001g0026 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(150): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(171): Show |
1 | a0001c0002t0001g0200 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(180): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(210): Show |
1 | a0001c0001t0001g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(219): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(192): Show |
1 | a0001c0002t0002g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(201): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(218): Show |
1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(227): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(166): Show |
1 | a0001c0003t0001g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(175): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(184): Show |
4 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0021t0001g0301others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5473-422_5473-421i others(193): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(196): Show |
1 | a0010c0025t0001g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(205): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(160): Show |
1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(169): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(203): Show |
1 | a0001c0001t0001g0236 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(212): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(209): Show |
1 | a0001c0001t0001g0229 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(218): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(210): Show |
23 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(20): Show | 23 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.5473-422_5473-421i others(219): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(221): Show |
5 | a0001c0001t0001g0238a0001c0001t0003g0002a0001c0001t0003g0003others(2): Show | 5 | NA18942.hp1 NA18952.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.5473-422_5473-421i others(230): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(211): Show |
1 | a0001c0001t0001g0083 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(220): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(209): Show |
1 | a0001c0001t0001g0237 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(218): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(199): Show |
1 | a0001c0001t0001g0276 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(208): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(201): Show |
1 | a0001c0019t0001g0274 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(210): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(158): Show |
4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(1): Show | 4 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.5473-422_5473-421i others(167): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(243): Show |
1 | a0001c0001t0001g0010 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(252): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(227): Show |
2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5473-422_5473-421i others(236): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(237): Show |
1 | a0001c0003t0001g0014 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(246): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(196): Show |
4 | a0001c0003t0001g0044a0001c0003t0001g0046a0001c0003t0001g0096others(1): Show | 4 | HG02647.hp2 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5473-422_5473-421i others(205): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(196): Show |
1 | a0001c0002t0001g0105 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(205): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(232): Show |
2 | a0001c0002t0001g0039a0001c0002t0001g0040 | 2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.5473-422_5473-421i others(241): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(183): Show |
1 | a0001c0045t0001g0327 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(192): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(218): Show |
1 | a0001c0002t0001g0036 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(227): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(190): Show |
1 | a0001c0002t0001g0120 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(199): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(158): Show |
1 | a0001c0001t0001g0011 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5473-422_5473-421i others(167): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(169): Show |
1 | a0001c0003t0001g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(178): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(170): Show |
1 | a0001c0003t0006g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(179): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(182): Show |
2 | a0001c0003t0001g0028a0001c0003t0001g0035 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5473-422_5473-421i others(191): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(184): Show |
3 | a0001c0003t0001g0029a0001c0003t0001g0032a0001c0035t0001g0030 | 3 | HG01109.hp1 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.5473-422_5473-421i others(193): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(195): Show |
2 | a0001c0003t0001g0033a0001c0016t0001g0006 | 2 | HG01099.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.5473-422_5473-421i others(204): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174910
|
T | TAATATAT others(161): Show |
1 | a0001c0003t0001g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5473-422_5473-421i others(170): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174910 | ||||||
| chr13:77174919
|
T | TTATATAT others(227): Show |
1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5473-431_5473-430i others(236): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174919 | ||||||
| chr13:77174921
|
A | ATATATAT others(188): Show |
1 | a0001c0002t0001g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5473-433_5473-432i others(197): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174921 | ||||||
| chr13:77174921
|
A | ATATATAT others(253): Show |
1 | a0001c0008t0001g0305 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.5473-433_5473-432i others(262): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174921 | ||||||
| chr13:77174921
|
A | ATATATAT others(228): Show |
7 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(4): Show | 7 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.5473-433_5473-432i others(237): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174921 | ||||||
| chr13:77174930
|
T | A | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.5473-441A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174930 | ||||||
| chr13:77174931
|
A | T | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.5473-442T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174931 | ||||||
| chr13:77174942
|
A | AAT | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.5473-454_5473-453i others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174942 | ||||||
| chr13:77174943
|
T | A | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.5473-454A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174943 | ||||||
| chr13:77174945
|
T | A | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.5473-456A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174945 | ||||||
| chr13:77174964
|
A | T | 101 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(98): Show | 102 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.5473-475T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77174964 | ||||||
| chr13:77175103
|
G | A | 202 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.5473-614C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77175103 | ||||||
| chr13:77175228
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.5473-739G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77175228 | ||||||
| chr13:77175229
|
G | A | 8 | a0001c0001t0001g0085a0001c0008t0001g0263a0001c0008t0001g0296others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.5473-740C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77175229 | ||||||
| chr13:77175701
|
T | C | 226 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.5472+796A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77175701 | ||||||
| chr13:77175750
|
C | T | 2 | a0001c0004t0001g0088a0001c0004t0001g0151 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5472+747G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77175750 | ||||||
| chr13:77175828
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5472+669C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77175828 | ||||||
| chr13:77175946
|
G | A | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5472+551C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77175946 | ||||||
| chr13:77175979
|
A | T | 86 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.5472+518T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77175979 | ||||||
| chr13:77176017
|
C | A | 1 | a0001c0001t0001g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.5472+480G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77176017 | ||||||
| chr13:77176019
|
C | CT | 87 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(84): Show | 87 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.5472+477dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77176019 | ||||||
| chr13:77176019
|
CT | C | 18 | a0001c0002t0001g0200a0001c0003t0001g0014a0001c0003t0001g0020others(15): Show | 18 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.5472+477delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77176019 | ||||||
| chr13:77176019
|
CTT | C | 34 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(31): Show | 34 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.5472+476_5472+477d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77176019 | ||||||
| chr13:77176020
|
T | A | 1 | a0001c0001t0001g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.5472+477A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77176020 | ||||||
| chr13:77176021
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.5472+476A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77176021 | ||||||
| chr13:77176177
|
C | A | 1 | a0016c0028t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5472+320G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77176177 | ||||||
| chr13:77176201
|
T | C | 1 | a0001c0002t0001g0120 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.5472+296A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77176201 | ||||||
| chr13:77176258
|
G | T | 1 | a0001c0033t0001g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5472+239C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 36/82 | chr13 | 77176258 | ||||||
| chr13:77176766
|
T | C | 291 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.5341-138A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77176766 | ||||||
| chr13:77176823
|
C | T | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.5341-195G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77176823 | ||||||
| chr13:77176921
|
G | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.5341-293C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77176921 | ||||||
| chr13:77177148
|
TA | T | 49 | a0001c0001t0001g0189a0001c0003t0001g0015a0001c0003t0001g0016others(46): Show | 49 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.5341-521delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77177148 | ||||||
| chr13:77177300
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5340+448T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77177300 | ||||||
| chr13:77177334
|
C | CT | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(15): Show | 19 | HG00438.hp1 HG01106.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.5340+413dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77177334 | ||||||
| chr13:77177334
|
CT | C | 23 | a0001c0001t0001g0007a0001c0001t0001g0080a0001c0001t0001g0141others(20): Show | 23 | HG00735.hp1 HG01934.hp1 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.5340+413delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77177334 | ||||||
| chr13:77177335
|
T | G | 1 | a0001c0003t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5340+413A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77177335 | ||||||
| chr13:77177435
|
G | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.5340+313C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77177435 | ||||||
| chr13:77177490
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.5340+258G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77177490 | ||||||
| chr13:77177503
|
G | A | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5340+245C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77177503 | ||||||
| chr13:77177663
|
G | C | 1 | a0001c0001t0001g0211 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.5340+85C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 35/82 | chr13 | 77177663 | ||||||
| chr13:77178051
|
A | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5134-97T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77178051 | ||||||
| chr13:77178146
|
C | G | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5134-192G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77178146 | ||||||
| chr13:77178342
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.5134-388A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77178342 | ||||||
| chr13:77178458
|
G | A | 1 | a0001c0002t0001g0049 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.5134-504C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77178458 | ||||||
| chr13:77178672
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5134-718T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77178672 | ||||||
| chr13:77178998
|
A | C | 6 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0093others(3): Show | 6 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.5134-1044T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77178998 | ||||||
| chr13:77179073
|
A | C | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.5133+1054T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77179073 | ||||||
| chr13:77179094
|
G | A | 1 | a0001c0005t0002g0133 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.5133+1033C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77179094 | ||||||
| chr13:77179161
|
T | C | 1 | a0001c0006t0001g0326 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.5133+966A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77179161 | ||||||
| chr13:77179202
|
A | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.5133+925T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77179202 | ||||||
| chr13:77179362
|
A | G | 1 | a0001c0001t0001g0238 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.5133+765T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77179362 | ||||||
| chr13:77179482
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.5133+645T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77179482 | ||||||
| chr13:77179868
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5133+259T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77179868 | ||||||
| chr13:77179977
|
G | A | 326 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.5133+150C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 34/82 | chr13 | 77179977 | ||||||
| chr13:77180399
|
T | C | 1 | a0001c0003t0001g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4942-81A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77180399 | ||||||
| chr13:77180456
|
A | G | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.4942-138T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77180456 | ||||||
| chr13:77180487
|
T | G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.4942-169A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77180487 | ||||||
| chr13:77180491
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4942-173A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77180491 | ||||||
| chr13:77180509
|
C | T | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.4942-191G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77180509 | ||||||
| chr13:77180607
|
C | G | 1 | a0017c0041t0001g0084 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.4942-289G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77180607 | ||||||
| chr13:77180750
|
A | G | 3 | a0001c0006t0001g0319a0001c0006t0001g0320a0001c0006t0001g0322 | 3 | HG01891.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4942-432T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77180750 | ||||||
| chr13:77180785
|
T | G | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4942-467A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77180785 | ||||||
| chr13:77180914
|
T | A | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4942-596A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77180914 | ||||||
| chr13:77181025
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0001g0245a0001c0001t0001g0246others(1): Show | 4 | NA18747.hp1 NA19000.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.4941+676A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77181025 | ||||||
| chr13:77181129
|
G | A | 2 | a0001c0003t0001g0022a0001c0003t0001g0023 | 2 | HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4941+572C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77181129 | ||||||
| chr13:77181337
|
G | T | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.4941+364C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77181337 | ||||||
| chr13:77181588
|
T | C | 50 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(47): Show | 50 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.4941+113A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 33/82 | chr13 | 77181588 | ||||||
| chr13:77182063
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4720-141A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182063 | ||||||
| chr13:77182219
|
A | G | 1 | a0001c0002t0001g0123 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4720-297T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182219 | ||||||
| chr13:77182239
|
C | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.4720-317G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182239 | ||||||
| chr13:77182425
|
C | T | 326 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.4720-503G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182425 | ||||||
| chr13:77182568
|
C | A | 1 | a0001c0002t0001g0115 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.4720-646G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182568 | ||||||
| chr13:77182654
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.4720-732G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182654 | ||||||
| chr13:77182725
|
T | A | 2 | a0001c0002t0001g0121a0001c0002t0001g0122 | 2 | NA19085.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.4720-803A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182725 | ||||||
| chr13:77182755
|
T | C | 1 | a0001c0002t0001g0257 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4720-833A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182755 | ||||||
| chr13:77182759
|
C | T | 20 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(17): Show | 20 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.4720-837G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182759 | ||||||
| chr13:77182770
|
G | A | 20 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(17): Show | 20 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.4720-848C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182770 | ||||||
| chr13:77182827
|
C | T | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4720-905G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182827 | ||||||
| chr13:77182906
|
A | G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.4720-984T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77182906 | ||||||
| chr13:77183051
|
T | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.4720-1129A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183051 | ||||||
| chr13:77183165
|
T | G | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4720-1243A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183165 | ||||||
| chr13:77183244
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.4720-1322G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183244 | ||||||
| chr13:77183458
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4720-1536T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183458 | ||||||
| chr13:77183541
|
C | CT | 93 | a0001c0001t0001g0085a0001c0001t0001g0090a0001c0001t0001g0091others(90): Show | 94 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.4719+1561dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
C | CTT | 95 | a0001c0001t0001g0034a0001c0001t0001g0089a0001c0001t0001g0093others(92): Show | 95 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.4719+1560_4719+156 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
C | CTTT | 26 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0130others(23): Show | 26 | HG00280.hp2 HG00438.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.4719+1559_4719+156 others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
C | CTTTTTTT others(4): Show |
2 | a0001c0003t0001g0022a0001c0003t0001g0023 | 2 | HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4719+1551_4719+156 others(15): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
C | CTTTTTTT others(5): Show |
3 | a0001c0003t0001g0016a0001c0003t0001g0020a0001c0003t0001g0021 | 3 | HG02717.hp2 HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.4719+1550_4719+156 others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
C | CTTTTTTT others(6): Show |
2 | a0001c0003t0001g0015a0001c0003t0001g0017 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4719+1549_4719+156 others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
C | CTTTTTTT others(13): Show |
1 | a0001c0003t0001g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4719+1542_4719+156 others(24): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
C | CTTTTTTT others(14): Show |
1 | a0001c0003t0001g0018 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4719+1541_4719+156 others(25): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
CT | C | 33 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(30): Show | 33 | HG00438.hp2 HG00735.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.4719+1561delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
CTT | C | 6 | a0001c0001t0001g0228a0001c0001t0003g0003a0001c0003t0001g0129others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4719+1560_4719+156 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
CTTT | C | 6 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(3): Show | 6 | HG00621.hp1 HG02132.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.4719+1559_4719+156 others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
CTTTTTT | C | 13 | a0001c0002t0001g0259a0001c0003t0001g0014a0001c0003t0001g0028others(10): Show | 13 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.4719+1556_4719+156 others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183541
|
CTTTTTTT others(2): Show |
C | 23 | a0001c0001t0001g0094a0001c0001t0001g0283a0001c0005t0002g0078others(20): Show | 23 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.4719+1553_4719+156 others(13): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183541 | ||||||
| chr13:77183542
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4719+1561A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183542 | ||||||
| chr13:77183585
|
T | C | 205 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.4719+1518A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183585 | ||||||
| chr13:77183662
|
G | A | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4719+1441C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183662 | ||||||
| chr13:77183771
|
C | T | 1 | a0018c0042t0001g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4719+1332G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183771 | ||||||
| chr13:77183930
|
C | A | 1 | a0001c0008t0001g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4719+1173G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77183930 | ||||||
| chr13:77184103
|
T | C | 1 | a0009c0022t0005g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4719+1000A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77184103 | ||||||
| chr13:77184501
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4719+602A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77184501 | ||||||
| chr13:77184561
|
G | T | 1 | a0001c0003t0001g0033 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4719+542C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77184561 | ||||||
| chr13:77184844
|
C | T | 6 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0305others(3): Show | 6 | HG02109.hp2 HG02818.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.4719+259G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77184844 | ||||||
| chr13:77185032
|
C | CA | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.4719+70dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 32/82 | chr13 | 77185032 | ||||||
| chr13:77185642
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4444+229C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 31/82 | chr13 | 77185642 | ||||||
| chr13:77185676
|
A | G | 1 | a0001c0003t0001g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4444+195T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 31/82 | chr13 | 77185676 | ||||||
| chr13:77185783
|
G | A | 2 | a0001c0006t0001g0317a0001c0006t0001g0318 | 2 | HG00642.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.4444+88C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 31/82 | chr13 | 77185783 | ||||||
| chr13:77186222
|
A | G | 1 | a0001c0004t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4252-159T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77186222 | ||||||
| chr13:77186234
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4252-171A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77186234 | ||||||
| chr13:77186562
|
A | G | 1 | a0001c0003t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4252-499T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77186562 | ||||||
| chr13:77186786
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.4252-723G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77186786 | ||||||
| chr13:77186790
|
T | C | 10 | a0001c0006t0001g0317a0001c0006t0001g0318a0001c0006t0001g0321others(7): Show | 10 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.4252-727A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77186790 | ||||||
| chr13:77186802
|
A | AT | 117 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(114): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.4252-740dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77186802 | ||||||
| chr13:77186802
|
AT | A | 29 | a0001c0001t0001g0081a0001c0001t0003g0002a0001c0002t0001g0103others(26): Show | 29 | HG00099.hp1 HG01069.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.4252-740delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77186802 | ||||||
| chr13:77186817
|
T | C | 1 | a0001c0003t0001g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4252-754A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77186817 | ||||||
| chr13:77186937
|
A | G | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.4252-874T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77186937 | ||||||
| chr13:77186965
|
C | T | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.4252-902G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77186965 | ||||||
| chr13:77187075
|
G | A | 85 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.4252-1012C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77187075 | ||||||
| chr13:77187680
|
G | A | 2 | a0001c0003t0001g0072a0012c0038t0002g0198 | 2 | HG01496.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4251+1271C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77187680 | ||||||
| chr13:77187734
|
A | C | 14 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(11): Show | 14 | HG00438.hp2 HG01255.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.4251+1217T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77187734 | ||||||
| chr13:77187877
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4251+1074G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77187877 | ||||||
| chr13:77187901
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.4251+1050A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77187901 | ||||||
| chr13:77187944
|
G | A | 20 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(17): Show | 20 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.4251+1007C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77187944 | ||||||
| chr13:77188002
|
C | T | 3 | a0001c0002t0001g0036a0001c0002t0001g0039a0001c0002t0001g0040 | 3 | HG00280.hp1 HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.4251+949G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77188002 | ||||||
| chr13:77188003
|
G | A | 8 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG02071.hp2 NA18960.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.4251+948C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77188003 | ||||||
| chr13:77188012
|
A | G | 2 | a0001c0005t0002g0222a0001c0005t0002g0224 | 2 | NA18952.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.4251+939T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77188012 | ||||||
| chr13:77188073
|
C | CA | 31 | a0001c0001t0001g0007a0001c0001t0001g0172a0001c0001t0001g0225others(28): Show | 31 | HG00099.hp1 HG01071.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.4251+877dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77188073 | ||||||
| chr13:77188171
|
T | C | 1 | a0001c0004t0001g0287 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4251+780A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77188171 | ||||||
| chr13:77188193
|
C | A | 1 | a0001c0006t0001g0321 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4251+758G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77188193 | ||||||
| chr13:77188350
|
A | G | 1 | a0001c0005t0002g0273 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4251+601T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77188350 | ||||||
| chr13:77188355
|
T | G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.4251+596A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77188355 | ||||||
| chr13:77188433
|
G | A | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4251+518C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77188433 | ||||||
| chr13:77188610
|
C | T | 25 | a0001c0002t0001g0102a0001c0002t0001g0103a0001c0002t0001g0105others(22): Show | 25 | HG00673.hp1 HG02015.hp1 HG02165.hp1 others(22): Show |
intron_variant | MODIFIER | c.4251+341G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 30/82 | chr13 | 77188610 | ||||||
| chr13:77189091
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4155-44A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 29/82 | chr13 | 77189091 | ||||||
| chr13:77189444
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4155-397G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 29/82 | chr13 | 77189444 | ||||||
| chr13:77189543
|
T | C | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.4155-496A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 29/82 | chr13 | 77189543 | ||||||
| chr13:77189553
|
G | A | 1 | a0001c0002t0001g0201 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4155-506C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 29/82 | chr13 | 77189553 | ||||||
| chr13:77189559
|
C | T | 1 | a0001c0026t0001g0285 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4155-512G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 29/82 | chr13 | 77189559 | ||||||
| chr13:77189897
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4154+355G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 29/82 | chr13 | 77189897 | ||||||
| chr13:77189962
|
A | C | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.4154+290T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 29/82 | chr13 | 77189962 | ||||||
| chr13:77190077
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4154+175T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 29/82 | chr13 | 77190077 | ||||||
| chr13:77190370
|
T | G | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4071-35A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 28/82 | chr13 | 77190370 | ||||||
| chr13:77190507
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4071-172C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 28/82 | chr13 | 77190507 | ||||||
| chr13:77190693
|
AGTCTGAA others(6): Show |
A | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4071-371_4071-359d others(15): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 28/82 | chr13 | 77190693 | ||||||
| chr13:77190733
|
T | A | 1 | a0001c0001t0001g0248 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4071-398A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 28/82 | chr13 | 77190733 | ||||||
| chr13:77191323
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.4070+356G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 28/82 | chr13 | 77191323 | ||||||
| chr13:77191591
|
A | G | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4070+88T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 28/82 | chr13 | 77191591 | ||||||
| chr13:77192679
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3936-866T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77192679 | ||||||
| chr13:77192940
|
T | C | 46 | a0001c0003t0001g0014a0001c0003t0001g0015a0001c0003t0001g0016others(43): Show | 46 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(43): Show |
intron_variant | MODIFIER | c.3936-1127A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77192940 | ||||||
| chr13:77193160
|
G | T | 10 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(7): Show | 10 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.3935+993C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77193160 | ||||||
| chr13:77193289
|
G | A | 78 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(75): Show | 78 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.3935+864C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77193289 | ||||||
| chr13:77193338
|
C | G | 1 | a0001c0001t0001g0081 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3935+815G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77193338 | ||||||
| chr13:77193396
|
C | T | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.3935+757G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77193396 | ||||||
| chr13:77193582
|
A | G | 1 | a0001c0002t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3935+571T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77193582 | ||||||
| chr13:77193589
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3935+564G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77193589 | ||||||
| chr13:77193614
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3935+539C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77193614 | ||||||
| chr13:77193676
|
G | A | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3935+477C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77193676 | ||||||
| chr13:77193694
|
A | C | 2 | a0001c0002t0001g0102a0001c0002t0001g0107 | 2 | HG02165.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.3935+459T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77193694 | ||||||
| chr13:77193733
|
C | A | 2 | a0001c0004t0001g0154a0001c0004t0001g0278 | 2 | HG00408.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.3935+420G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77193733 | ||||||
| chr13:77193854
|
A | G | 206 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.3935+299T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77193854 | ||||||
| chr13:77194037
|
T | C | 52 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(49): Show | 52 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.3935+116A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 27/82 | chr13 | 77194037 | ||||||
| chr13:77194293
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0255 | 2 | NA18943.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.3844-49G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77194293 | ||||||
| chr13:77194669
|
C | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.3844-425G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77194669 | ||||||
| chr13:77194981
|
T | G | 1 | a0001c0005t0002g0136 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3844-737A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77194981 | ||||||
| chr13:77195024
|
C | CT | 44 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(41): Show | 44 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.3844-781dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195024 | ||||||
| chr13:77195024
|
CT | C | 113 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(110): Show | 113 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.3844-781delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195024 | ||||||
| chr13:77195137
|
G | A | 1 | a0001c0023t0001g0206 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3844-893C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195137 | ||||||
| chr13:77195219
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3844-975G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195219 | ||||||
| chr13:77195287
|
T | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.3844-1043A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195287 | ||||||
| chr13:77195292
|
T | G | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.3844-1048A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195292 | ||||||
| chr13:77195357
|
G | C | 1 | a0001c0033t0001g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3844-1113C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195357 | ||||||
| chr13:77195367
|
C | A | 2 | a0001c0003t0001g0020a0001c0003t0001g0021 | 2 | HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3844-1123G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195367 | ||||||
| chr13:77195406
|
G | A | 2 | a0001c0012t0001g0074a0001c0012t0001g0075 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3844-1162C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195406 | ||||||
| chr13:77195458
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3844-1214C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195458 | ||||||
| chr13:77195460
|
G | T | 2 | a0001c0002t0001g0048a0001c0002t0001g0067 | 2 | NA18979.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.3844-1216C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195460 | ||||||
| chr13:77195524
|
G | A | 17 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(14): Show | 17 | HG00735.hp2 HG02109.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.3844-1280C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195524 | ||||||
| chr13:77195591
|
T | TA | 80 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(77): Show | 80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.3844-1348dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195591 | ||||||
| chr13:77195615
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3844-1371G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195615 | ||||||
| chr13:77195649
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3844-1405T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77195649 | ||||||
| chr13:77196054
|
T | C | 1 | a0001c0003t0001g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3844-1810A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77196054 | ||||||
| chr13:77196585
|
C | G | 76 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(73): Show | 76 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.3844-2341G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77196585 | ||||||
| chr13:77196629
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3844-2385G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77196629 | ||||||
| chr13:77196720
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0255 | 2 | NA18943.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.3844-2476C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77196720 | ||||||
| chr13:77196722
|
T | TTGGGAGG others(242): Show |
2 | a0001c0001t0001g0095a0001c0001t0001g0255 | 2 | NA18943.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.3844-2479_3844-247 others(253): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77196722 | ||||||
| chr13:77196724
|
T | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0255 | 2 | NA18943.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.3844-2480A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77196724 | ||||||
| chr13:77196864
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3844-2620C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77196864 | ||||||
| chr13:77196977
|
C | A | 2 | a0001c0005t0002g0223a0001c0005t0002g0271 | 2 | NA18995.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3844-2733G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77196977 | ||||||
| chr13:77197035
|
G | A | 1 | a0001c0009t0001g0128 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3844-2791C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197035 | ||||||
| chr13:77197037
|
G | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3844-2793C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197037 | ||||||
| chr13:77197129
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3844-2885A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197129 | ||||||
| chr13:77197251
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3844-3007A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197251 | ||||||
| chr13:77197281
|
G | C | 4 | a0001c0003t0001g0028a0001c0003t0001g0032a0001c0003t0001g0035others(1): Show | 4 | HG01109.hp1 HG01243.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3844-3037C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197281 | ||||||
| chr13:77197389
|
C | T | 14 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(11): Show | 14 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3844-3145G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197389 | ||||||
| chr13:77197399
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3844-3155T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197399 | ||||||
| chr13:77197605
|
T | C | 9 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(6): Show | 9 | HG01071.hp2 HG01261.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.3844-3361A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197605 | ||||||
| chr13:77197609
|
C | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3844-3365G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197609 | ||||||
| chr13:77197647
|
G | A | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3844-3403C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197647 | ||||||
| chr13:77197707
|
A | G | 39 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(36): Show | 39 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.3844-3463T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197707 | ||||||
| chr13:77197793
|
G | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3844-3549C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197793 | ||||||
| chr13:77197794
|
A | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3844-3550T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197794 | ||||||
| chr13:77197845
|
T | C | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3844-3601A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197845 | ||||||
| chr13:77197917
|
A | C | 1 | a0001c0002t0001g0203 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3844-3673T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197917 | ||||||
| chr13:77197994
|
C | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0280 | 2 | HG01255.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.3844-3750G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77197994 | ||||||
| chr13:77198192
|
T | C | 2 | a0001c0009t0001g0077a0001c0009t0001g0127 | 2 | HG02523.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.3844-3948A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77198192 | ||||||
| chr13:77198319
|
T | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 41 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.3844-4075A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77198319 | ||||||
| chr13:77198405
|
G | T | 39 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(36): Show | 39 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.3844-4161C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77198405 | ||||||
| chr13:77198542
|
A | G | 1 | a0002c0040t0001g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3844-4298T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77198542 | ||||||
| chr13:77198670
|
G | A | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.3844-4426C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77198670 | ||||||
| chr13:77198687
|
T | C | 1 | a0001c0003t0001g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3844-4443A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77198687 | ||||||
| chr13:77198935
|
G | C | 39 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(36): Show | 39 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.3844-4691C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77198935 | ||||||
| chr13:77199027
|
G | A | 2 | a0001c0003t0001g0015a0001c0003t0001g0017 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3844-4783C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199027 | ||||||
| chr13:77199027
|
G | C | 1 | a0001c0001t0001g0144 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3844-4783C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199027 | ||||||
| chr13:77199074
|
C | A | 4 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(1): Show | 4 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3844-4830G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199074 | ||||||
| chr13:77199158
|
C | G | 1 | a0001c0002t0001g0054 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3844-4914G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199158 | ||||||
| chr13:77199187
|
C | A | 1 | a0001c0002t0001g0049 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3844-4943G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199187 | ||||||
| chr13:77199192
|
C | T | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.3844-4948G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199192 | ||||||
| chr13:77199322
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.3844-5078G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199322 | ||||||
| chr13:77199332
|
A | G | 1 | a0001c0003t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3844-5088T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199332 | ||||||
| chr13:77199395
|
T | C | 206 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.3844-5151A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199395 | ||||||
| chr13:77199407
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3844-5163C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199407 | ||||||
| chr13:77199447
|
C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3844-5203G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199447 | ||||||
| chr13:77199470
|
C | T | 1 | a0001c0043t0001g0292 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3844-5226G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199470 | ||||||
| chr13:77199643
|
T | A | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3844-5399A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199643 | ||||||
| chr13:77199692
|
T | C | 1 | a0016c0028t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3844-5448A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199692 | ||||||
| chr13:77199700
|
A | T | 1 | a0001c0001t0001g0247 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3844-5456T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199700 | ||||||
| chr13:77199702
|
G | A | 1 | a0001c0004t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3844-5458C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199702 | ||||||
| chr13:77199706
|
G | C | 1 | a0001c0002t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3844-5462C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199706 | ||||||
| chr13:77199742
|
T | C | 326 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3844-5498A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199742 | ||||||
| chr13:77199787
|
C | T | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.3843+5469G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199787 | ||||||
| chr13:77199919
|
C | A | 3 | a0001c0005t0002g0136a0001c0009t0001g0076a0014c0032t0001g0038 | 3 | HG00621.hp1 HG02109.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.3843+5337G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199919 | ||||||
| chr13:77199922
|
T | C | 1 | a0001c0009t0001g0076 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3843+5334A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199922 | ||||||
| chr13:77199953
|
A | G | 1 | a0001c0003t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3843+5303T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199953 | ||||||
| chr13:77199976
|
G | C | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.3843+5280C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77199976 | ||||||
| chr13:77200055
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3843+5201C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200055 | ||||||
| chr13:77200101
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3843+5155C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200101 | ||||||
| chr13:77200207
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3843+5049C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200207 | ||||||
| chr13:77200262
|
C | T | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3843+4994G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200262 | ||||||
| chr13:77200266
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3843+4990C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200266 | ||||||
| chr13:77200267
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3843+4989T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200267 | ||||||
| chr13:77200316
|
G | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.3843+4940C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200316 | ||||||
| chr13:77200323
|
G | A | 74 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(71): Show | 74 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.3843+4933C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200323 | ||||||
| chr13:77200340
|
G | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.3843+4916C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200340 | ||||||
| chr13:77200370
|
C | T | 1 | a0011c0024t0001g0092 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3843+4886G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200370 | ||||||
| chr13:77200418
|
G | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0247 | 2 | HG00597.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.3843+4838C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200418 | ||||||
| chr13:77200435
|
T | C | 41 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(38): Show | 41 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.3843+4821A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200435 | ||||||
| chr13:77200542
|
C | T | 119 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 119 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.3843+4714G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200542 | ||||||
| chr13:77200560
|
T | C | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0003g0002others(3): Show | 6 | HG01257.hp1 NA18942.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.3843+4696A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200560 | ||||||
| chr13:77200597
|
T | C | 1 | a0001c0003t0001g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3843+4659A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200597 | ||||||
| chr13:77200649
|
C | T | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.3843+4607G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200649 | ||||||
| chr13:77200666
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3843+4590C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200666 | ||||||
| chr13:77200762
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3843+4494G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200762 | ||||||
| chr13:77200785
|
C | A | 1 | a0014c0032t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3843+4471G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200785 | ||||||
| chr13:77200893
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3843+4363A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200893 | ||||||
| chr13:77200903
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3843+4353C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200903 | ||||||
| chr13:77200926
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3843+4330G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200926 | ||||||
| chr13:77200927
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3843+4329T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200927 | ||||||
| chr13:77200984
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3843+4272A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200984 | ||||||
| chr13:77200988
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3843+4268G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200988 | ||||||
| chr13:77200989
|
G | A | 1 | a0001c0002t0001g0202 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3843+4267C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77200989 | ||||||
| chr13:77201005
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3843+4251A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201005 | ||||||
| chr13:77201024
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3843+4232G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201024 | ||||||
| chr13:77201048
|
A | C | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3843+4208T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201048 | ||||||
| chr13:77201073
|
C | T | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3843+4183G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201073 | ||||||
| chr13:77201099
|
C | A | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3843+4157G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201099 | ||||||
| chr13:77201105
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3843+4151C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201105 | ||||||
| chr13:77201135
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3843+4121C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201135 | ||||||
| chr13:77201154
|
C | T | 2 | a0001c0001t0001g0239a0001c0036t0001g0291 | 2 | HG01257.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.3843+4102G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201154 | ||||||
| chr13:77201165
|
G | A | 51 | a0001c0001t0001g0239a0001c0003t0001g0015a0001c0003t0001g0016others(48): Show | 51 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.3843+4091C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201165 | ||||||
| chr13:77201168
|
T | C | 332 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.3843+4088A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201168 | ||||||
| chr13:77201182
|
A | G | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3843+4074T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201182 | ||||||
| chr13:77201310
|
T | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3843+3946A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201310 | ||||||
| chr13:77201378
|
C | A | 155 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(152): Show | 155 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.3843+3878G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201378 | ||||||
| chr13:77201415
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0251 | 2 | HG00738.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.3843+3841C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201415 | ||||||
| chr13:77201449
|
C | T | 85 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.3843+3807G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201449 | ||||||
| chr13:77201539
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3843+3717C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201539 | ||||||
| chr13:77201630
|
C | T | 2 | a0001c0002t0001g0117a0008c0039t0001g0118 | 2 | NA18953.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.3843+3626G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201630 | ||||||
| chr13:77201631
|
A | G | 2 | a0001c0002t0001g0117a0008c0039t0001g0118 | 2 | NA18953.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.3843+3625T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201631 | ||||||
| chr13:77201691
|
G | A | 49 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(46): Show | 49 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.3843+3565C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201691 | ||||||
| chr13:77201749
|
C | G | 1 | a0001c0002t0001g0199 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3843+3507G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201749 | ||||||
| chr13:77201858
|
G | A | 2 | a0001c0004t0001g0157a0001c0004t0001g0265 | 2 | HG00099.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3843+3398C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201858 | ||||||
| chr13:77201860
|
A | C | 1 | a0001c0004t0001g0265 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3843+3396T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77201860 | ||||||
| chr13:77202139
|
G | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3843+3117C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202139 | ||||||
| chr13:77202185
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3843+3071C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202185 | ||||||
| chr13:77202190
|
A | C | 1 | a0016c0028t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3843+3066T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202190 | ||||||
| chr13:77202218
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3843+3038C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202218 | ||||||
| chr13:77202268
|
C | T | 1 | a0001c0003t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3843+2988G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202268 | ||||||
| chr13:77202329
|
C | T | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3843+2927G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202329 | ||||||
| chr13:77202379
|
A | C | 2 | a0001c0004t0001g0293a0001c0004t0001g0303 | 2 | HG01952.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.3843+2877T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202379 | ||||||
| chr13:77202422
|
A | G | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3843+2834T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202422 | ||||||
| chr13:77202505
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3843+2751T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202505 | ||||||
| chr13:77202519
|
A | C | 1 | a0007c0018t0003g0004 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3843+2737T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202519 | ||||||
| chr13:77202598
|
G | T | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3843+2658C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202598 | ||||||
| chr13:77202743
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.3843+2513A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202743 | ||||||
| chr13:77202946
|
T | C | 1 | a0001c0002t0001g0026 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3843+2310A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77202946 | ||||||
| chr13:77203007
|
C | A | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3843+2249G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203007 | ||||||
| chr13:77203026
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3843+2230A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203026 | ||||||
| chr13:77203050
|
T | C | 5 | a0001c0005t0002g0222a0001c0005t0002g0224a0001c0005t0002g0268others(2): Show | 5 | NA18952.hp1 NA18982.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.3843+2206A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203050 | ||||||
| chr13:77203092
|
A | G | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.3843+2164T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203092 | ||||||
| chr13:77203120
|
C | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0190a0001c0001t0001g0250 | 3 | NA18955.hp1 NA18961.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.3843+2136G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203120 | ||||||
| chr13:77203130
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3843+2126C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203130 | ||||||
| chr13:77203171
|
T | C | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | NA18954.hp2 NA18964.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.3843+2085A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203171 | ||||||
| chr13:77203352
|
C | G | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3843+1904G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203352 | ||||||
| chr13:77203384
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3843+1872C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203384 | ||||||
| chr13:77203399
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3843+1857A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203399 | ||||||
| chr13:77203573
|
A | T | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0304 | 3 | HG00673.hp2 NA18945.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.3843+1683T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203573 | ||||||
| chr13:77203581
|
A | T | 1 | a0001c0002t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3843+1675T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203581 | ||||||
| chr13:77203582
|
G | T | 1 | a0001c0002t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3843+1674C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203582 | ||||||
| chr13:77203583
|
A | G | 1 | a0001c0002t0001g0063 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3843+1673T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203583 | ||||||
| chr13:77203686
|
A | C | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3843+1570T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203686 | ||||||
| chr13:77203715
|
G | A | 2 | a0001c0004t0001g0265a0001c0036t0001g0291 | 2 | HG01071.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.3843+1541C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203715 | ||||||
| chr13:77203827
|
A | G | 1 | a0001c0002t0001g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3843+1429T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203827 | ||||||
| chr13:77203866
|
C | T | 58 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0089others(55): Show | 58 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.3843+1390G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203866 | ||||||
| chr13:77203867
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3843+1389G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203867 | ||||||
| chr13:77203886
|
A | G | 1 | a0001c0001t0001g0294 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3843+1370T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203886 | ||||||
| chr13:77203972
|
G | A | 1 | a0001c0003t0001g0207 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3843+1284C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203972 | ||||||
| chr13:77203997
|
T | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3843+1259A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77203997 | ||||||
| chr13:77204031
|
A | C | 1 | a0001c0002t0001g0060 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3843+1225T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204031 | ||||||
| chr13:77204080
|
A | C | 2 | a0001c0013t0001g0191a0001c0013t0001g0192 | 2 | NA18968.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.3843+1176T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204080 | ||||||
| chr13:77204190
|
C | A | 11 | a0001c0002t0001g0061a0001c0008t0001g0263a0001c0008t0001g0296others(8): Show | 11 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.3843+1066G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204190 | ||||||
| chr13:77204273
|
T | A | 1 | a0001c0002t0001g0202 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3843+983A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204273 | ||||||
| chr13:77204342
|
A | T | 1 | a0018c0042t0001g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3843+914T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204342 | ||||||
| chr13:77204437
|
T | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3843+819A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204437 | ||||||
| chr13:77204616
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.3843+640A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204616 | ||||||
| chr13:77204639
|
A | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.3843+617T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204639 | ||||||
| chr13:77204726
|
T | G | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3843+530A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204726 | ||||||
| chr13:77204768
|
AATC | A | 4 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3843+485_3843+487d others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204768 | ||||||
| chr13:77204815
|
G | A | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.3843+441C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204815 | ||||||
| chr13:77204825
|
A | G | 26 | a0001c0002t0001g0102a0001c0002t0001g0103a0001c0002t0001g0105others(23): Show | 26 | HG00673.hp1 HG02015.hp1 HG02165.hp1 others(23): Show |
intron_variant | MODIFIER | c.3843+431T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204825 | ||||||
| chr13:77204840
|
T | C | 1 | a0001c0002t0001g0119 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3843+416A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77204840 | ||||||
| chr13:77205023
|
A | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3843+233T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77205023 | ||||||
| chr13:77205026
|
TAC | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.3843+228_3843+229d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77205026 | ||||||
| chr13:77205063
|
A | C | 41 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 41 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.3843+193T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 26/82 | chr13 | 77205063 | ||||||
| chr13:77205409
|
G | A | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3716-26C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 25/82 | chr13 | 77205409 | ||||||
| chr13:77205442
|
G | C | 1 | a0001c0001t0001g0248 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3715+31C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 25/82 | chr13 | 77205442 | ||||||
| chr13:77205673
|
T | C | 1 | a0001c0002t0002g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3590-75A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 24/82 | chr13 | 77205673 | ||||||
| chr13:77205734
|
T | A | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3590-136A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 24/82 | chr13 | 77205734 | ||||||
| chr13:77205751
|
C | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3590-153G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 24/82 | chr13 | 77205751 | ||||||
| chr13:77205922
|
G | A | 1 | a0001c0008t0001g0296 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3590-324C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 24/82 | chr13 | 77205922 | ||||||
| chr13:77205968
|
G | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3590-370C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 24/82 | chr13 | 77205968 | ||||||
| chr13:77206014
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3590-416T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 24/82 | chr13 | 77206014 | ||||||
| chr13:77206333
|
ATAAAT | A | 7 | a0001c0002t0001g0105a0001c0002t0001g0108a0001c0002t0001g0115others(4): Show | 7 | HG01978.hp1 NA18963.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.3589+315_3589+319d others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 24/82 | chr13 | 77206333 | ||||||
| chr13:77206420
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3589+233A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 24/82 | chr13 | 77206420 | ||||||
| chr13:77206530
|
T | C | 6 | a0001c0001t0001g0043a0001c0001t0001g0160a0001c0001t0001g0162others(3): Show | 6 | HG00741.hp2 HG01106.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.3589+123A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 24/82 | chr13 | 77206530 | ||||||
| chr13:77206580
|
T | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.3589+73A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 24/82 | chr13 | 77206580 | ||||||
| chr13:77206874
|
A | T | 34 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(31): Show | 34 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(31): Show |
intron_variant | MODIFIER | c.3417-49T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77206874 | ||||||
| chr13:77206972
|
CTAAACAT others(1): Show |
C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.3417-155_3417-148d others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77206972 | ||||||
| chr13:77207035
|
T | C | 3 | a0002c0007t0001g0212a0002c0007t0001g0217a0002c0007t0001g0219 | 3 | HG02486.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3417-210A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77207035 | ||||||
| chr13:77207798
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.3417-973A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77207798 | ||||||
| chr13:77208148
|
T | G | 1 | a0001c0009t0001g0310 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3417-1323A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77208148 | ||||||
| chr13:77208161
|
T | G | 207 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.3417-1336A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77208161 | ||||||
| chr13:77208192
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3417-1367T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77208192 | ||||||
| chr13:77208490
|
C | T | 5 | a0001c0005t0002g0222a0001c0005t0002g0224a0001c0005t0002g0268others(2): Show | 5 | NA18952.hp1 NA18982.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.3417-1665G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77208490 | ||||||
| chr13:77208491
|
A | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.3417-1666T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77208491 | ||||||
| chr13:77208755
|
GA | G | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3417-1931delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77208755 | ||||||
| chr13:77208881
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3417-2056A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77208881 | ||||||
| chr13:77209324
|
A | G | 1 | a0001c0005t0002g0224 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3416+1843T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77209324 | ||||||
| chr13:77209620
|
C | G | 1 | a0006c0017t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3416+1547G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77209620 | ||||||
| chr13:77209836
|
G | A | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3416+1331C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77209836 | ||||||
| chr13:77209964
|
C | T | 14 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(11): Show | 14 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3416+1203G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77209964 | ||||||
| chr13:77210147
|
A | G | 2 | a0003c0010t0001g0111a0003c0010t0001g0112 | 2 | NA18943.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.3416+1020T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210147 | ||||||
| chr13:77210193
|
AT | A | 36 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0081others(33): Show | 36 | HG00438.hp2 HG01255.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.3416+973delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210193 | ||||||
| chr13:77210232
|
G | A | 6 | a0001c0003t0001g0018a0001c0003t0001g0019a0001c0003t0001g0020others(3): Show | 6 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3416+935C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210232 | ||||||
| chr13:77210337
|
T | C | 2 | a0001c0002t0001g0069a0001c0029t0001g0065 | 2 | HG01515.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.3416+830A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210337 | ||||||
| chr13:77210353
|
C | A | 151 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(148): Show | 151 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.3416+814G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210353 | ||||||
| chr13:77210365
|
C | T | 2 | a0001c0001t0001g0282a0001c0004t0001g0154 | 2 | HG00408.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.3416+802G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210365 | ||||||
| chr13:77210383
|
A | G | 3 | a0001c0003t0001g0207a0001c0003t0006g0209a0001c0034t0001g0024 | 3 | HG02622.hp1 HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3416+784T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210383 | ||||||
| chr13:77210393
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3416+774A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210393 | ||||||
| chr13:77210394
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3416+773C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210394 | ||||||
| chr13:77210408
|
G | A | 1 | a0001c0002t0001g0110 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3416+759C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210408 | ||||||
| chr13:77210414
|
G | A | 1 | a0001c0002t0001g0110 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3416+753C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210414 | ||||||
| chr13:77210487
|
C | T | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3416+680G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210487 | ||||||
| chr13:77210618
|
G | GT | 2 | a0001c0002t0001g0001a0001c0002t0001g0114 | 3 | HG03490.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.3416+548dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210618 | ||||||
| chr13:77210741
|
T | A | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.3416+426A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210741 | ||||||
| chr13:77210761
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3416+406C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210761 | ||||||
| chr13:77210804
|
T | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0300 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3416+363A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210804 | ||||||
| chr13:77210829
|
C | T | 1 | a0014c0032t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3416+338G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210829 | ||||||
| chr13:77210856
|
C | T | 330 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.3416+311G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210856 | ||||||
| chr13:77210894
|
T | A | 1 | a0001c0002t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3416+273A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210894 | ||||||
| chr13:77210931
|
C | T | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.3416+236G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210931 | ||||||
| chr13:77210942
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0068 | 2 | HG02738.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3416+225A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210942 | ||||||
| chr13:77210957
|
A | T | 86 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.3416+210T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 23/82 | chr13 | 77210957 | ||||||
| chr13:77211523
|
T | G | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3263-203A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 22/82 | chr13 | 77211523 | ||||||
| chr13:77211871
|
A | G | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3262+85T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 22/82 | chr13 | 77211871 | ||||||
| chr13:77212243
|
A | G | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3058-83T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77212243 | ||||||
| chr13:77212319
|
G | T | 20 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(17): Show | 20 | HG00099.hp1 HG01496.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.3058-159C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77212319 | ||||||
| chr13:77212391
|
A | T | 1 | a0001c0002t0001g0115 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3058-231T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77212391 | ||||||
| chr13:77212417
|
G | A | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3058-257C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77212417 | ||||||
| chr13:77212541
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.3058-381A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77212541 | ||||||
| chr13:77212908
|
G | A | 2 | a0001c0003t0001g0018a0001c0003t0001g0019 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3058-748C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77212908 | ||||||
| chr13:77212932
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3058-772A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77212932 | ||||||
| chr13:77213304
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3058-1144C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77213304 | ||||||
| chr13:77213419
|
G | A | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3058-1259C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77213419 | ||||||
| chr13:77213464
|
T | C | 326 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3058-1304A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77213464 | ||||||
| chr13:77213691
|
C | T | 39 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(36): Show | 39 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.3058-1531G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77213691 | ||||||
| chr13:77214015
|
AG | A | 5 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0249others(2): Show | 5 | HG00738.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3058-1856delC | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77214015 | ||||||
| chr13:77214033
|
A | C | 4 | a0001c0001t0001g0168a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG00609.hp1 HG02080.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.3058-1873T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77214033 | ||||||
| chr13:77214302
|
T | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3058-2142A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77214302 | ||||||
| chr13:77214409
|
T | C | 1 | a0004c0011t0001g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3058-2249A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77214409 | ||||||
| chr13:77214450
|
TA | T | 30 | a0001c0001t0001g0085a0001c0001t0001g0238a0001c0001t0003g0002others(27): Show | 30 | HG00735.hp1 HG00735.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.3058-2291delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77214450 | ||||||
| chr13:77214597
|
T | G | 1 | a0001c0003t0001g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3058-2437A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77214597 | ||||||
| chr13:77214695
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0253 | 2 | HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3058-2535G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77214695 | ||||||
| chr13:77214701
|
A | AG | 41 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(38): Show | 41 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.3058-2542_3058-254 others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77214701 | ||||||
| chr13:77215001
|
G | A | 10 | a0001c0003t0001g0207a0001c0003t0006g0209a0001c0008t0001g0263others(7): Show | 10 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.3057+2839C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77215001 | ||||||
| chr13:77215056
|
T | A | 1 | a0001c0004t0001g0150 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3057+2784A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77215056 | ||||||
| chr13:77215167
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3057+2673A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77215167 | ||||||
| chr13:77215469
|
T | C | 2 | a0001c0001t0001g0286a0001c0001t0001g0300 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.3057+2371A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77215469 | ||||||
| chr13:77215894
|
A | T | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.3057+1946T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77215894 | ||||||
| chr13:77215931
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3057+1909G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77215931 | ||||||
| chr13:77216143
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3057+1697G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77216143 | ||||||
| chr13:77216397
|
T | C | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.3057+1443A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77216397 | ||||||
| chr13:77216414
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3057+1426T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77216414 | ||||||
| chr13:77216431
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3057+1409A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77216431 | ||||||
| chr13:77217040
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3057+800G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77217040 | ||||||
| chr13:77217081
|
C | A | 1 | a0001c0004t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3057+759G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77217081 | ||||||
| chr13:77217613
|
A | C | 8 | a0002c0007t0001g0212a0002c0007t0001g0213a0002c0007t0001g0214others(5): Show | 8 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3057+227T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 21/82 | chr13 | 77217613 | ||||||
| chr13:77217964
|
T | A | 1 | a0001c0002t0001g0200 | 1 | NA19001.hp2 | splice_region_variant&intron_variant | LOW | c.2940-7A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77217964 | ||||||
| chr13:77217964
|
T | C | 29 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0102others(26): Show | 29 | HG00597.hp2 HG00673.hp1 HG02015.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.2940-7A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77217964 | ||||||
| chr13:77218047
|
A | G | 1 | a0001c0002t0001g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2940-90T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218047 | ||||||
| chr13:77218233
|
A | G | 1 | a0001c0002t0001g0049 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2940-276T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218233 | ||||||
| chr13:77218263
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2940-306G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218263 | ||||||
| chr13:77218271
|
C | T | 7 | a0001c0002t0001g0048a0001c0002t0001g0059a0001c0002t0001g0064others(4): Show | 7 | HG00558.hp1 HG01515.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2940-314G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218271 | ||||||
| chr13:77218347
|
A | G | 1 | a0001c0003t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2940-390T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218347 | ||||||
| chr13:77218499
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2940-542G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218499 | ||||||
| chr13:77218511
|
C | T | 1 | a0001c0003t0001g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2940-554G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218511 | ||||||
| chr13:77218649
|
A | G | 1 | a0001c0023t0001g0206 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2940-692T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218649 | ||||||
| chr13:77218834
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2940-877G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218834 | ||||||
| chr13:77218862
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2940-905T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218862 | ||||||
| chr13:77218976
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2940-1019A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218976 | ||||||
| chr13:77218978
|
G | A | 1 | a0001c0029t0001g0065 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2940-1021C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77218978 | ||||||
| chr13:77219009
|
A | T | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2940-1052T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77219009 | ||||||
| chr13:77219055
|
T | C | 1 | a0001c0005t0002g0272 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2940-1098A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77219055 | ||||||
| chr13:77219163
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2940-1206C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77219163 | ||||||
| chr13:77219205
|
A | T | 1 | a0001c0004t0001g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2940-1248T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77219205 | ||||||
| chr13:77219237
|
T | C | 85 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2940-1280A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77219237 | ||||||
| chr13:77219505
|
A | G | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.2940-1548T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77219505 | ||||||
| chr13:77219569
|
A | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2940-1612T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77219569 | ||||||
| chr13:77219768
|
T | G | 2 | a0001c0012t0001g0074a0001c0012t0001g0075 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2940-1811A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77219768 | ||||||
| chr13:77219821
|
T | C | 1 | a0001c0002t0001g0171 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2940-1864A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77219821 | ||||||
| chr13:77220008
|
T | C | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2940-2051A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77220008 | ||||||
| chr13:77220085
|
TAAGTATA others(3): Show |
T | 2 | a0001c0002t0001g0048a0001c0002t0001g0067 | 2 | NA18979.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2940-2138_2940-212 others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77220085 | ||||||
| chr13:77220414
|
C | A | 4 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0164others(1): Show | 4 | HG01243.hp2 HG01261.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.2940-2457G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77220414 | ||||||
| chr13:77220433
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2940-2476G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77220433 | ||||||
| chr13:77220471
|
A | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2940-2514T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77220471 | ||||||
| chr13:77220698
|
G | A | 11 | a0001c0001t0001g0043a0001c0001t0001g0090a0001c0001t0001g0160others(8): Show | 11 | HG00741.hp2 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.2940-2741C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77220698 | ||||||
| chr13:77220780
|
T | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2940-2823A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77220780 | ||||||
| chr13:77220947
|
T | G | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2940-2990A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77220947 | ||||||
| chr13:77221101
|
A | G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2940-3144T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77221101 | ||||||
| chr13:77221253
|
C | T | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.2939+3198G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77221253 | ||||||
| chr13:77221366
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2939+3085C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77221366 | ||||||
| chr13:77221395
|
A | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2939+3056T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77221395 | ||||||
| chr13:77221400
|
C | T | 1 | a0009c0022t0005g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2939+3051G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77221400 | ||||||
| chr13:77221453
|
C | T | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2939+2998G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77221453 | ||||||
| chr13:77221550
|
C | T | 2 | a0001c0001t0004g0181a0001c0001t0004g0184 | 2 | NA18942.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.2939+2901G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77221550 | ||||||
| chr13:77221601
|
G | T | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2939+2850C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77221601 | ||||||
| chr13:77221855
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2939+2596A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77221855 | ||||||
| chr13:77221992
|
T | A | 12 | a0001c0003t0001g0014a0001c0003t0001g0028a0001c0003t0001g0029others(9): Show | 12 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2939+2459A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77221992 | ||||||
| chr13:77222174
|
T | C | 1 | a0001c0002t0001g0049 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2939+2277A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222174 | ||||||
| chr13:77222203
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2939+2248A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222203 | ||||||
| chr13:77222298
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2939+2153A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222298 | ||||||
| chr13:77222334
|
A | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2939+2117T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222334 | ||||||
| chr13:77222375
|
G | C | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2939+2076C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222375 | ||||||
| chr13:77222407
|
TAAG | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(70): Show | 73 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.2939+2041_2939+204 others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222407 | ||||||
| chr13:77222485
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2939+1966G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222485 | ||||||
| chr13:77222605
|
G | C | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2939+1846C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222605 | ||||||
| chr13:77222611
|
G | A | 4 | a0001c0001t0001g0168a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG00609.hp1 HG02080.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.2939+1840C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222611 | ||||||
| chr13:77222628
|
C | T | 4 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2939+1823G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222628 | ||||||
| chr13:77222635
|
C | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2939+1816G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222635 | ||||||
| chr13:77222667
|
A | G | 1 | a0001c0005t0002g0269 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2939+1784T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222667 | ||||||
| chr13:77222709
|
AT | A | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2939+1741delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222709 | ||||||
| chr13:77222903
|
C | T | 1 | a0001c0002t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2939+1548G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222903 | ||||||
| chr13:77222934
|
C | A | 39 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(36): Show | 39 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.2939+1517G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77222934 | ||||||
| chr13:77223415
|
A | C | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2939+1036T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77223415 | ||||||
| chr13:77223584
|
C | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2939+867G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77223584 | ||||||
| chr13:77223608
|
G | C | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2939+843C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77223608 | ||||||
| chr13:77223907
|
TA | T | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.2939+543delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77223907 | ||||||
| chr13:77223909
|
A | C | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.2939+542T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77223909 | ||||||
| chr13:77223910
|
A | C | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.2939+541T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77223910 | ||||||
| chr13:77223913
|
TAA | T | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.2939+536_2939+537d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77223913 | ||||||
| chr13:77223917
|
A | C | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.2939+534T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 20/82 | chr13 | 77223917 | ||||||
| chr13:77224705
|
T | C | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2858-173A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 19/82 | chr13 | 77224705 | ||||||
| chr13:77224761
|
G | T | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.2858-229C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 19/82 | chr13 | 77224761 | ||||||
| chr13:77224762
|
T | G | 6 | a0001c0006t0001g0319a0001c0006t0001g0320a0001c0006t0001g0322others(3): Show | 6 | HG01891.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2858-230A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 19/82 | chr13 | 77224762 | ||||||
| chr13:77225190
|
G | C | 2 | a0001c0003t0001g0018a0001c0003t0001g0019 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2857+245C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 19/82 | chr13 | 77225190 | ||||||
| chr13:77225633
|
G | A | 2 | a0001c0002t0001g0069a0001c0029t0001g0065 | 2 | HG01515.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.2738-79C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77225633 | ||||||
| chr13:77225761
|
TA | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2738-208delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77225761 | ||||||
| chr13:77225876
|
G | T | 1 | a0001c0004t0001g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2738-322C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77225876 | ||||||
| chr13:77226019
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2738-465T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77226019 | ||||||
| chr13:77226044
|
T | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2738-490A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77226044 | ||||||
| chr13:77226233
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2738-679A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77226233 | ||||||
| chr13:77226571
|
T | C | 1 | a0001c0045t0001g0327 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2738-1017A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77226571 | ||||||
| chr13:77226974
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2738-1420T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77226974 | ||||||
| chr13:77227343
|
TA | T | 31 | a0001c0001t0001g0089a0001c0001t0001g0282a0001c0003t0001g0031others(28): Show | 31 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.2738-1790delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227343 | ||||||
| chr13:77227393
|
T | G | 39 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(36): Show | 39 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(36): Show |
intron_variant | MODIFIER | c.2738-1839A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227393 | ||||||
| chr13:77227481
|
T | TAC | 29 | a0001c0002t0001g0025a0001c0002t0001g0048a0001c0002t0001g0055others(26): Show | 29 | HG00099.hp1 HG00558.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.2738-1929_2738-192 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227481 | ||||||
| chr13:77227481
|
T | TACAC | 9 | a0001c0002t0001g0068a0001c0003t0001g0015a0001c0003t0001g0016others(6): Show | 9 | HG02109.hp1 HG02717.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2738-1931_2738-192 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227481 | ||||||
| chr13:77227481
|
TAC | T | 25 | a0001c0001t0001g0315a0001c0002t0001g0061a0001c0003t0001g0028others(22): Show | 25 | HG00735.hp2 HG00741.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.2738-1929_2738-192 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227481 | ||||||
| chr13:77227481
|
TACAC | T | 37 | a0001c0001t0001g0085a0001c0001t0001g0140a0001c0001t0001g0234others(34): Show | 37 | HG00609.hp2 HG00621.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2738-1931_2738-192 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227481 | ||||||
| chr13:77227481
|
TACACAC | T | 139 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 139 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2738-1933_2738-192 others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227481 | ||||||
| chr13:77227481
|
TACACACA others(1): Show |
T | 9 | a0001c0001t0001g0143a0001c0001t0001g0160a0001c0001t0001g0162others(6): Show | 9 | HG01106.hp1 HG01516.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2738-1935_2738-192 others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227481 | ||||||
| chr13:77227481
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0001g0173a0001c0001t0001g0252 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2738-1937_2738-192 others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227481 | ||||||
| chr13:77227515
|
C | T | 4 | a0001c0006t0001g0323a0001c0006t0001g0324a0001c0006t0001g0325others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.2738-1961G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227515 | ||||||
| chr13:77227559
|
G | A | 6 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(3): Show | 6 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.2738-2005C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227559 | ||||||
| chr13:77227683
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2738-2129C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227683 | ||||||
| chr13:77227916
|
A | G | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2738-2362T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227916 | ||||||
| chr13:77227969
|
T | C | 1 | a0001c0002t0001g0052 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2738-2415A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77227969 | ||||||
| chr13:77228036
|
C | A | 111 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(108): Show | 111 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.2738-2482G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228036 | ||||||
| chr13:77228176
|
C | G | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.2738-2622G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228176 | ||||||
| chr13:77228278
|
G | A | 1 | a0001c0004t0001g0287 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2738-2724C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228278 | ||||||
| chr13:77228498
|
C | G | 6 | a0001c0002t0001g0052a0001c0002t0001g0054a0001c0002t0001g0055others(3): Show | 6 | HG00609.hp2 HG02155.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.2738-2944G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228498 | ||||||
| chr13:77228506
|
C | CA | 26 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(23): Show | 26 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2738-2953dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228506 | ||||||
| chr13:77228506
|
CA | C | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2738-2953delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228506 | ||||||
| chr13:77228691
|
T | TTG | 20 | a0001c0001t0001g0298a0001c0002t0001g0025a0001c0002t0001g0026others(17): Show | 20 | HG00099.hp1 HG00544.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2738-3139_2738-313 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228691 | ||||||
| chr13:77228691
|
T | TTGTG | 4 | a0001c0002t0001g0036a0001c0002t0001g0201a0001c0044t0001g0332others(1): Show | 4 | HG00280.hp1 HG02293.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.2738-3141_2738-313 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228691 | ||||||
| chr13:77228691
|
TTG | T | 57 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 57 | HG00733.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.2738-3139_2738-313 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228691 | ||||||
| chr13:77228691
|
TTGTG | T | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0034others(151): Show | 154 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.2738-3141_2738-313 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228691 | ||||||
| chr13:77228766
|
C | T | 1 | a0001c0004t0001g0155 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2738-3212G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228766 | ||||||
| chr13:77228928
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2738-3374G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77228928 | ||||||
| chr13:77229112
|
T | C | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2738-3558A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77229112 | ||||||
| chr13:77229373
|
G | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2737+3783C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77229373 | ||||||
| chr13:77229431
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2737+3725A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77229431 | ||||||
| chr13:77229469
|
C | T | 86 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.2737+3687G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77229469 | ||||||
| chr13:77229569
|
T | C | 1 | a0001c0002t0001g0119 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2737+3587A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77229569 | ||||||
| chr13:77229864
|
G | T | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2737+3292C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77229864 | ||||||
| chr13:77229959
|
C | G | 2 | a0001c0006t0001g0330a0001c0006t0001g0331 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2737+3197G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77229959 | ||||||
| chr13:77230102
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2737+3054C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77230102 | ||||||
| chr13:77230252
|
C | T | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2737+2904G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77230252 | ||||||
| chr13:77230264
|
A | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012 | 3 | HG01891.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2737+2892T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77230264 | ||||||
| chr13:77230407
|
T | C | 1 | a0001c0009t0001g0128 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2737+2749A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77230407 | ||||||
| chr13:77230646
|
T | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0256 | 2 | NA18963.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2737+2510A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77230646 | ||||||
| chr13:77230886
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2737+2270A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77230886 | ||||||
| chr13:77231078
|
T | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2737+2078A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77231078 | ||||||
| chr13:77231380
|
G | A | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2737+1776C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77231380 | ||||||
| chr13:77231778
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2737+1378C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77231778 | ||||||
| chr13:77231863
|
C | T | 1 | a0002c0007t0001g0219 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2737+1293G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77231863 | ||||||
| chr13:77232536
|
G | A | 1 | a0001c0003t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2737+620C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77232536 | ||||||
| chr13:77232616
|
G | A | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2737+540C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77232616 | ||||||
| chr13:77232929
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2737+227T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 18/82 | chr13 | 77232929 | ||||||
| chr13:77233542
|
A | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(8): Show | 11 | HG00544.hp1 HG02015.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.2630-279T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77233542 | ||||||
| chr13:77233770
|
C | T | 1 | a0001c0021t0001g0301 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2630-507G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77233770 | ||||||
| chr13:77233877
|
C | CGA | 86 | a0001c0001t0001g0283a0001c0002t0001g0001a0001c0002t0001g0025others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.2630-616_2630-615d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77233877 | ||||||
| chr13:77233985
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2630-722T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77233985 | ||||||
| chr13:77233988
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2630-725C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77233988 | ||||||
| chr13:77234212
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2630-949A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77234212 | ||||||
| chr13:77234309
|
T | A | 4 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(1): Show | 4 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2630-1046A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77234309 | ||||||
| chr13:77234358
|
A | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2630-1095T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77234358 | ||||||
| chr13:77234464
|
T | C | 50 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(47): Show | 50 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.2630-1201A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77234464 | ||||||
| chr13:77234508
|
T | C | 1 | a0001c0001t0001g0314 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2630-1245A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77234508 | ||||||
| chr13:77234565
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2630-1302T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77234565 | ||||||
| chr13:77234844
|
T | TAA | 229 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2630-1582_2630-158 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77234844 | ||||||
| chr13:77235025
|
A | C | 1 | a0002c0007t0001g0213 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2630-1762T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77235025 | ||||||
| chr13:77235097
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2630-1834T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77235097 | ||||||
| chr13:77235117
|
T | A | 9 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.2630-1854A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77235117 | ||||||
| chr13:77235119
|
T | C | 2 | a0001c0001t0001g0034a0001c0004t0001g0174 | 2 | HG01255.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2630-1856A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77235119 | ||||||
| chr13:77235231
|
A | T | 2 | a0001c0001t0001g0276a0001c0019t0001g0274 | 2 | HG02155.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.2630-1968T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77235231 | ||||||
| chr13:77235484
|
A | G | 1 | a0009c0022t0005g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2630-2221T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77235484 | ||||||
| chr13:77235524
|
A | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2630-2261T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77235524 | ||||||
| chr13:77235540
|
T | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0239 | 2 | HG01257.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2630-2277A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77235540 | ||||||
| chr13:77236120
|
T | C | 2 | a0001c0008t0001g0263a0001c0008t0001g0296 | 2 | HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2630-2857A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77236120 | ||||||
| chr13:77236290
|
C | T | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2630-3027G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77236290 | ||||||
| chr13:77236438
|
C | G | 3 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0203 | 3 | HG02027.hp1 NA18947.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2630-3175G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77236438 | ||||||
| chr13:77236628
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2630-3365C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77236628 | ||||||
| chr13:77236830
|
C | T | 1 | a0001c0005t0002g0224 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2630-3567G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77236830 | ||||||
| chr13:77236876
|
T | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0255 | 2 | NA18943.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2630-3613A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77236876 | ||||||
| chr13:77237304
|
G | T | 325 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(322): Show | 326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.2630-4041C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77237304 | ||||||
| chr13:77237331
|
G | C | 6 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0305others(3): Show | 6 | HG02109.hp2 HG02818.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2630-4068C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77237331 | ||||||
| chr13:77237393
|
T | C | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2630-4130A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77237393 | ||||||
| chr13:77237560
|
G | A | 4 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(1): Show | 4 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2630-4297C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77237560 | ||||||
| chr13:77237808
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2630-4545A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77237808 | ||||||
| chr13:77237811
|
T | C | 1 | a0014c0032t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2630-4548A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77237811 | ||||||
| chr13:77237831
|
A | C | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2630-4568T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77237831 | ||||||
| chr13:77237868
|
T | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0013 | 2 | HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2630-4605A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77237868 | ||||||
| chr13:77237924
|
C | T | 1 | a0001c0003t0001g0041 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2630-4661G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77237924 | ||||||
| chr13:77238010
|
A | C | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.2630-4747T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77238010 | ||||||
| chr13:77238019
|
G | A | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2630-4756C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77238019 | ||||||
| chr13:77238238
|
G | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2629+4821C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77238238 | ||||||
| chr13:77238242
|
C | CA | 39 | a0001c0001t0001g0011a0001c0001t0001g0140a0001c0001t0001g0143others(36): Show | 39 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.2629+4816dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77238242 | ||||||
| chr13:77238242
|
C | CAA | 15 | a0001c0003t0001g0016a0001c0003t0001g0027a0001c0003t0001g0031others(12): Show | 15 | HG00735.hp1 HG00735.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2629+4815_2629+481 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77238242 | ||||||
| chr13:77238310
|
A | G | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2629+4749T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77238310 | ||||||
| chr13:77238391
|
T | C | 5 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0249others(2): Show | 5 | HG00738.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2629+4668A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77238391 | ||||||
| chr13:77238533
|
C | A | 1 | a0001c0002t0001g0025 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2629+4526G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77238533 | ||||||
| chr13:77238686
|
T | A | 14 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(11): Show | 14 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2629+4373A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77238686 | ||||||
| chr13:77238727
|
C | T | 30 | a0001c0003t0001g0031a0001c0005t0002g0078a0001c0005t0002g0079others(27): Show | 30 | HG00099.hp1 HG00735.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.2629+4332G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77238727 | ||||||
| chr13:77238833
|
C | A | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2629+4226G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77238833 | ||||||
| chr13:77239010
|
C | T | 7 | a0001c0002t0001g0103a0001c0002t0001g0110a0001c0002t0001g0120others(4): Show | 7 | HG00673.hp1 HG02015.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.2629+4049G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77239010 | ||||||
| chr13:77239012
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0001g0294 | 2 | HG00280.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2629+4047G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77239012 | ||||||
| chr13:77239033
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2629+4026A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77239033 | ||||||
| chr13:77239199
|
A | G | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.2629+3860T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77239199 | ||||||
| chr13:77239293
|
A | G | 6 | a0001c0002t0001g0052a0001c0002t0001g0054a0001c0002t0001g0055others(3): Show | 6 | HG00609.hp2 HG02155.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.2629+3766T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77239293 | ||||||
| chr13:77239365
|
C | T | 1 | a0001c0002t0001g0058 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2629+3694G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77239365 | ||||||
| chr13:77239452
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2629+3607G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77239452 | ||||||
| chr13:77239559
|
C | T | 8 | a0001c0002t0001g0117a0001c0002t0001g0121a0001c0002t0001g0122others(5): Show | 8 | NA18953.hp1 NA18960.hp2 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.2629+3500G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77239559 | ||||||
| chr13:77239673
|
T | G | 50 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(47): Show | 50 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.2629+3386A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77239673 | ||||||
| chr13:77239676
|
C | T | 85 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2629+3383G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77239676 | ||||||
| chr13:77239836
|
T | A | 29 | a0001c0001t0001g0280a0001c0002t0001g0149a0001c0004t0001g0087others(26): Show | 29 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.2629+3223A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77239836 | ||||||
| chr13:77240009
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2629+3050A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77240009 | ||||||
| chr13:77240130
|
A | G | 12 | a0001c0003t0001g0014a0001c0003t0001g0028a0001c0003t0001g0029others(9): Show | 12 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2629+2929T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77240130 | ||||||
| chr13:77240195
|
A | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2629+2864T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77240195 | ||||||
| chr13:77240424
|
A | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2629+2635T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77240424 | ||||||
| chr13:77240425
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2629+2634A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77240425 | ||||||
| chr13:77240437
|
G | A | 1 | a0001c0029t0001g0065 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2629+2622C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77240437 | ||||||
| chr13:77240568
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2629+2491C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77240568 | ||||||
| chr13:77240762
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2629+2297A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77240762 | ||||||
| chr13:77241241
|
A | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.2629+1818T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77241241 | ||||||
| chr13:77241332
|
C | A | 50 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(47): Show | 50 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.2629+1727G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77241332 | ||||||
| chr13:77241714
|
A | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2629+1345T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77241714 | ||||||
| chr13:77241715
|
C | T | 2 | a0001c0005t0002g0269a0001c0005t0002g0270 | 2 | NA18983.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2629+1344G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77241715 | ||||||
| chr13:77241850
|
G | GA | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2629+1208dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77241850 | ||||||
| chr13:77242079
|
G | A | 30 | a0001c0003t0001g0129a0001c0005t0002g0078a0001c0005t0002g0079others(27): Show | 30 | HG00099.hp1 HG00621.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.2629+980C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77242079 | ||||||
| chr13:77242158
|
G | C | 1 | a0001c0002t0001g0120 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2629+901C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77242158 | ||||||
| chr13:77242270
|
C | T | 2 | a0001c0002t0001g0001a0001c0002t0001g0114 | 3 | HG03490.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2629+789G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77242270 | ||||||
| chr13:77242447
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2629+612T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77242447 | ||||||
| chr13:77242485
|
A | T | 1 | a0001c0001t0001g0146 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2629+574T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77242485 | ||||||
| chr13:77242626
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2629+433A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77242626 | ||||||
| chr13:77242639
|
T | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.2629+420A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77242639 | ||||||
| chr13:77242722
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2629+337G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77242722 | ||||||
| chr13:77242801
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2629+258A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77242801 | ||||||
| chr13:77242903
|
T | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2629+156A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77242903 | ||||||
| chr13:77242940
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2629+119G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 17/82 | chr13 | 77242940 | ||||||
| chr13:77243210
|
A | T | 1 | a0001c0003t0001g0033 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2528-50T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 16/82 | chr13 | 77243210 | ||||||
| chr13:77243375
|
G | A | 5 | a0001c0005t0002g0222a0001c0005t0002g0224a0001c0005t0002g0268others(2): Show | 5 | NA18952.hp1 NA18982.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.2528-215C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 16/82 | chr13 | 77243375 | ||||||
| chr13:77243391
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2528-231A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 16/82 | chr13 | 77243391 | ||||||
| chr13:77243446
|
C | A | 85 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(82): Show | 86 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2528-286G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 16/82 | chr13 | 77243446 | ||||||
| chr13:77243545
|
G | A | 113 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(110): Show | 113 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.2527+261C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 16/82 | chr13 | 77243545 | ||||||
| chr13:77243620
|
G | GA | 66 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(63): Show | 67 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.2527+185dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 16/82 | chr13 | 77243620 | ||||||
| chr13:77243655
|
T | C | 4 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(1): Show | 4 | HG01928.hp2 HG01934.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2527+151A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 16/82 | chr13 | 77243655 | ||||||
| chr13:77243673
|
C | T | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2527+133G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 16/82 | chr13 | 77243673 | ||||||
| chr13:77243789
|
T | C | 1 | a0001c0002t0001g0123 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2527+17A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 16/82 | chr13 | 77243789 | ||||||
| chr13:77243965
|
C | CA | 165 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(162): Show | 165 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.2382-15dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77243965 | ||||||
| chr13:77243965
|
C | CAA | 15 | a0001c0001t0001g0197a0001c0003t0001g0017a0001c0003t0001g0027others(12): Show | 15 | HG00621.hp2 HG00735.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.2382-16_2382-15dup others(2): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77243965 | ||||||
| chr13:77243965
|
CA | C | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2382-15delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77243965 | ||||||
| chr13:77244201
|
C | T | 2 | a0001c0012t0001g0074a0001c0012t0001g0075 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2382-250G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77244201 | ||||||
| chr13:77244232
|
A | C | 1 | a0001c0001t0001g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2382-281T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77244232 | ||||||
| chr13:77244292
|
C | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(70): Show | 73 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.2382-341G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77244292 | ||||||
| chr13:77244667
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2382-716C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77244667 | ||||||
| chr13:77244723
|
C | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2382-772G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77244723 | ||||||
| chr13:77244810
|
C | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2382-859G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77244810 | ||||||
| chr13:77245139
|
G | A | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2382-1188C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245139 | ||||||
| chr13:77245286
|
C | T | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2382-1335G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245286 | ||||||
| chr13:77245309
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0300 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2382-1358G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245309 | ||||||
| chr13:77245599
|
C | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2382-1648G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245599 | ||||||
| chr13:77245604
|
TG | T | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.2382-1654delC | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245604 | ||||||
| chr13:77245744
|
AAC | A | 15 | a0001c0001t0001g0165a0001c0002t0001g0110a0001c0002t0001g0125others(12): Show | 15 | HG00673.hp1 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.2382-1795_2382-179 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245744 | ||||||
| chr13:77245744
|
AACAC | A | 126 | a0001c0001t0001g0095a0001c0001t0001g0143a0001c0001t0001g0158others(123): Show | 127 | HG00099.hp1 HG00597.hp2 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.2382-1797_2382-179 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245744 | ||||||
| chr13:77245744
|
AACACAC | A | 126 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0034others(123): Show | 126 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.2382-1799_2382-179 others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245744 | ||||||
| chr13:77245744
|
AACACACA others(1): Show |
A | 53 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(50): Show | 53 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.2382-1801_2382-179 others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245744 | ||||||
| chr13:77245744
|
AACACACA others(3): Show |
A | 1 | a0001c0003t0001g0072 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2382-1803_2382-179 others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245744 | ||||||
| chr13:77245744
|
AACACACA others(5): Show |
A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2382-1805_2382-179 others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245744 | ||||||
| chr13:77245836
|
G | GTA | 11 | a0001c0003t0001g0207a0001c0003t0006g0209a0001c0009t0001g0076others(8): Show | 11 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2382-1887_2382-188 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245836 | ||||||
| chr13:77245851
|
TAC | T | 109 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(106): Show | 109 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.2382-1902_2382-190 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245851 | ||||||
| chr13:77245873
|
T | TAC | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2382-1924_2382-192 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77245873 | ||||||
| chr13:77246192
|
C | T | 14 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(11): Show | 14 | HG00438.hp2 HG01255.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.2382-2241G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77246192 | ||||||
| chr13:77246228
|
C | T | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2382-2277G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77246228 | ||||||
| chr13:77246337
|
T | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2382-2386A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77246337 | ||||||
| chr13:77246415
|
G | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2382-2464C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77246415 | ||||||
| chr13:77246427
|
C | A | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2382-2476G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77246427 | ||||||
| chr13:77246539
|
AAGG | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2382-2591_2382-258 others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77246539 | ||||||
| chr13:77246672
|
C | CA | 8 | a0001c0001t0001g0043a0001c0001t0001g0290a0001c0002t0001g0026others(5): Show | 8 | HG00544.hp1 HG00544.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.2382-2722dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77246672 | ||||||
| chr13:77246684
|
C | A | 9 | a0001c0002t0002g0053a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2382-2733G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77246684 | ||||||
| chr13:77246718
|
G | A | 1 | a0001c0003t0001g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2382-2767C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77246718 | ||||||
| chr13:77247039
|
C | T | 3 | a0004c0011t0001g0148a0004c0011t0001g0152a0012c0038t0002g0198 | 3 | HG01496.hp2 NA18950.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.2382-3088G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77247039 | ||||||
| chr13:77247159
|
A | T | 1 | a0001c0045t0001g0327 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2382-3208T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77247159 | ||||||
| chr13:77247170
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2382-3219G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77247170 | ||||||
| chr13:77247302
|
G | A | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2382-3351C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77247302 | ||||||
| chr13:77247409
|
C | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2382-3458G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77247409 | ||||||
| chr13:77247470
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2382-3519C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77247470 | ||||||
| chr13:77247546
|
G | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2382-3595C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77247546 | ||||||
| chr13:77247934
|
CA | C | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2381+3216delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77247934 | ||||||
| chr13:77247943
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2381+3208T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77247943 | ||||||
| chr13:77248142
|
C | CA | 202 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(199): Show | 203 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.2381+3008dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77248142 | ||||||
| chr13:77248142
|
C | CAA | 117 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0034others(114): Show | 117 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.2381+3007_2381+300 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77248142 | ||||||
| chr13:77248200
|
A | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2381+2951T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77248200 | ||||||
| chr13:77248581
|
C | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2381+2570G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77248581 | ||||||
| chr13:77248659
|
T | C | 1 | a0001c0023t0001g0206 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2381+2492A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77248659 | ||||||
| chr13:77248688
|
G | C | 1 | a0012c0038t0002g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2381+2463C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77248688 | ||||||
| chr13:77248690
|
GA | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0164others(1): Show | 4 | HG01243.hp2 HG01261.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.2381+2460delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77248690 | ||||||
| chr13:77248698
|
G | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2381+2453C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77248698 | ||||||
| chr13:77248767
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.2381+2384A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77248767 | ||||||
| chr13:77248797
|
AG | A | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.2381+2353delC | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77248797 | ||||||
| chr13:77248860
|
C | G | 154 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(151): Show | 154 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.2381+2291G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77248860 | ||||||
| chr13:77249041
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2381+2110A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77249041 | ||||||
| chr13:77249290
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2381+1861T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77249290 | ||||||
| chr13:77249719
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2381+1432G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77249719 | ||||||
| chr13:77249937
|
T | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2381+1214A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77249937 | ||||||
| chr13:77249950
|
G | A | 1 | a0001c0002t0001g0205 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2381+1201C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77249950 | ||||||
| chr13:77250073
|
A | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0237 | 2 | HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.2381+1078T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250073 | ||||||
| chr13:77250124
|
G | A | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2381+1027C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250124 | ||||||
| chr13:77250201
|
C | T | 1 | a0001c0009t0001g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2381+950G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250201 | ||||||
| chr13:77250222
|
C | CA | 116 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(113): Show | 116 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.2381+928dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250222 | ||||||
| chr13:77250239
|
T | A | 4 | a0001c0002t0001g0056a0001c0002t0001g0057a0001c0002t0001g0062others(1): Show | 4 | HG00423.hp1 NA18978.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2381+912A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250239 | ||||||
| chr13:77250266
|
G | C | 20 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(17): Show | 20 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2381+885C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250266 | ||||||
| chr13:77250458
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2381+693G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250458 | ||||||
| chr13:77250746
|
T | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.2381+405A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250746 | ||||||
| chr13:77250764
|
C | T | 1 | a0001c0045t0001g0327 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2381+387G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250764 | ||||||
| chr13:77250820
|
T | A | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2381+331A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250820 | ||||||
| chr13:77250844
|
G | A | 4 | a0001c0002t0001g0102a0001c0002t0001g0107a0001c0002t0001g0123others(1): Show | 4 | HG02165.hp1 NA18612.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.2381+307C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250844 | ||||||
| chr13:77250914
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2381+237A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250914 | ||||||
| chr13:77250919
|
T | G | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2381+232A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77250919 | ||||||
| chr13:77251073
|
A | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2381+78T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77251073 | ||||||
| chr13:77251081
|
A | T | 29 | a0001c0001t0001g0280a0001c0002t0001g0149a0001c0004t0001g0087others(26): Show | 29 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.2381+70T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77251081 | ||||||
| chr13:77251088
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2381+63C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77251088 | ||||||
| chr13:77251099
|
G | A | 1 | a0001c0006t0001g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2381+52C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77251099 | ||||||
| chr13:77251133
|
G | C | 2 | a0001c0001t0001g0095a0001c0001t0001g0255 | 2 | NA18943.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2381+18C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77251133 | ||||||
| chr13:77251142
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2381+9C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 15/82 | chr13 | 77251142 | ||||||
| chr13:77251460
|
C | A | 1 | a0001c0003t0001g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2177-105G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77251460 | ||||||
| chr13:77251551
|
A | G | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2177-196T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77251551 | ||||||
| chr13:77251790
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2177-435G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77251790 | ||||||
| chr13:77251875
|
C | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2177-520G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77251875 | ||||||
| chr13:77252019
|
C | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2177-664G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77252019 | ||||||
| chr13:77252564
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2177-1209G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77252564 | ||||||
| chr13:77252647
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2177-1292G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77252647 | ||||||
| chr13:77252722
|
G | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2177-1367C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77252722 | ||||||
| chr13:77252755
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2177-1400T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77252755 | ||||||
| chr13:77253021
|
A | G | 1 | a0010c0025t0001g0086 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2177-1666T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77253021 | ||||||
| chr13:77253138
|
C | T | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2177-1783G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77253138 | ||||||
| chr13:77253225
|
G | T | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2177-1870C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77253225 | ||||||
| chr13:77253256
|
A | G | 4 | a0002c0007t0001g0213a0002c0007t0001g0214a0002c0007t0001g0216others(1): Show | 4 | HG00735.hp1 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2177-1901T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77253256 | ||||||
| chr13:77253380
|
T | A | 1 | a0001c0002t0001g0056 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2177-2025A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77253380 | ||||||
| chr13:77253614
|
GGCT | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2177-2262_2177-226 others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77253614 | ||||||
| chr13:77253823
|
T | C | 1 | a0001c0004t0001g0287 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2177-2468A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77253823 | ||||||
| chr13:77254049
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.2177-2694A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77254049 | ||||||
| chr13:77254136
|
G | A | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2177-2781C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77254136 | ||||||
| chr13:77254141
|
T | C | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | NA18954.hp2 NA18964.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.2177-2786A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77254141 | ||||||
| chr13:77254179
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2177-2824A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77254179 | ||||||
| chr13:77254347
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2177-2992C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77254347 | ||||||
| chr13:77254377
|
T | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.2177-3022A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77254377 | ||||||
| chr13:77254564
|
C | T | 2 | a0001c0003t0001g0020a0001c0003t0001g0021 | 2 | HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2176+3107G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77254564 | ||||||
| chr13:77254759
|
C | T | 86 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.2176+2912G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77254759 | ||||||
| chr13:77254914
|
C | A | 14 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(11): Show | 14 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2176+2757G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77254914 | ||||||
| chr13:77255671
|
T | G | 20 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(17): Show | 20 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2176+2000A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77255671 | ||||||
| chr13:77255743
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2176+1928G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77255743 | ||||||
| chr13:77255842
|
G | C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2176+1829C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77255842 | ||||||
| chr13:77255854
|
G | A | 1 | a0014c0032t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2176+1817C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77255854 | ||||||
| chr13:77255875
|
A | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0013 | 2 | HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2176+1796T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77255875 | ||||||
| chr13:77255894
|
T | C | 1 | a0001c0001t0001g0238 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2176+1777A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77255894 | ||||||
| chr13:77255992
|
C | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2176+1679G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77255992 | ||||||
| chr13:77256241
|
C | A | 1 | a0001c0033t0001g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2176+1430G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77256241 | ||||||
| chr13:77256241
|
C | T | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.2176+1430G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77256241 | ||||||
| chr13:77256315
|
T | C | 1 | a0001c0004t0001g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2176+1356A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77256315 | ||||||
| chr13:77256482
|
T | C | 1 | a0016c0028t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2176+1189A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77256482 | ||||||
| chr13:77256504
|
G | T | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2176+1167C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77256504 | ||||||
| chr13:77256523
|
T | C | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2176+1148A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77256523 | ||||||
| chr13:77256576
|
A | G | 4 | a0001c0006t0001g0323a0001c0006t0001g0324a0001c0006t0001g0325others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.2176+1095T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77256576 | ||||||
| chr13:77256606
|
T | C | 1 | a0001c0003t0001g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2176+1065A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77256606 | ||||||
| chr13:77256700
|
C | T | 1 | a0001c0045t0001g0327 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2176+971G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77256700 | ||||||
| chr13:77256906
|
A | C | 3 | a0001c0005t0002g0221a0001c0005t0002g0272a0001c0005t0002g0273 | 3 | HG01928.hp1 HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.2176+765T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77256906 | ||||||
| chr13:77257054
|
A | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.2176+617T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77257054 | ||||||
| chr13:77257104
|
T | C | 4 | a0001c0002t0001g0056a0001c0002t0001g0057a0001c0002t0001g0062others(1): Show | 4 | HG00423.hp1 NA18978.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2176+567A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77257104 | ||||||
| chr13:77257278
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2176+393A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77257278 | ||||||
| chr13:77257374
|
T | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2176+297A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77257374 | ||||||
| chr13:77257503
|
A | C | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2176+168T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77257503 | ||||||
| chr13:77257584
|
G | A | 1 | a0001c0002t0001g0199 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2176+87C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77257584 | ||||||
| chr13:77257621
|
A | G | 7 | a0001c0002t0001g0103a0001c0002t0001g0110a0001c0002t0001g0120others(4): Show | 7 | HG00673.hp1 HG02015.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.2176+50T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 14/82 | chr13 | 77257621 | ||||||
| chr13:77257853
|
T | C | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2018-24A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77257853 | ||||||
| chr13:77257926
|
A | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0255 | 2 | NA18943.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2018-97T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77257926 | ||||||
| chr13:77258155
|
G | T | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2018-326C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77258155 | ||||||
| chr13:77258229
|
T | C | 1 | a0001c0006t0001g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2018-400A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77258229 | ||||||
| chr13:77258458
|
ACAAT | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2018-633_2018-630d others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77258458 | ||||||
| chr13:77258711
|
G | A | 77 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(74): Show | 77 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.2018-882C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77258711 | ||||||
| chr13:77258769
|
G | A | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2018-940C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77258769 | ||||||
| chr13:77258925
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2018-1096C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77258925 | ||||||
| chr13:77258945
|
T | C | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2018-1116A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77258945 | ||||||
| chr13:77258997
|
G | A | 1 | a0001c0005t0002g0222 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2018-1168C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77258997 | ||||||
| chr13:77259200
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2017+1228C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77259200 | ||||||
| chr13:77259330
|
A | G | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2017+1098T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77259330 | ||||||
| chr13:77259697
|
T | A | 49 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(46): Show | 49 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.2017+731A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77259697 | ||||||
| chr13:77259992
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0178 | 2 | HG02165.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2017+436G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77259992 | ||||||
| chr13:77260113
|
T | G | 146 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(143): Show | 146 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.2017+315A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 13/82 | chr13 | 77260113 | ||||||
| chr13:77260600
|
A | G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1853-8T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 12/82 | chr13 | 77260600 | ||||||
| chr13:77260621
|
G | T | 1 | a0001c0002t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1853-29C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 12/82 | chr13 | 77260621 | ||||||
| chr13:77260753
|
C | T | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1853-161G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 12/82 | chr13 | 77260753 | ||||||
| chr13:77260762
|
T | C | 4 | a0001c0001t0001g0168a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG00609.hp1 HG02080.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1853-170A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 12/82 | chr13 | 77260762 | ||||||
| chr13:77260878
|
C | T | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1853-286G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 12/82 | chr13 | 77260878 | ||||||
| chr13:77261385
|
T | TA | 220 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1648-11dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 11/82 | chr13 | 77261385 | ||||||
| chr13:77261385
|
T | TAA | 10 | a0001c0001t0001g0253a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1648-12_1648-11dup others(2): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 11/82 | chr13 | 77261385 | ||||||
| chr13:77261453
|
A | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.1648-78T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 11/82 | chr13 | 77261453 | ||||||
| chr13:77261498
|
C | A | 1 | a0001c0003t0001g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1648-123G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 11/82 | chr13 | 77261498 | ||||||
| chr13:77261661
|
A | G | 1 | a0001c0002t0001g0201 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1648-286T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 11/82 | chr13 | 77261661 | ||||||
| chr13:77261747
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1647+306T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 11/82 | chr13 | 77261747 | ||||||
| chr13:77261992
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1647+61T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 11/82 | chr13 | 77261992 | ||||||
| chr13:77261998
|
T | C | 50 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(47): Show | 50 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1647+55A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 11/82 | chr13 | 77261998 | ||||||
| chr13:77262153
|
C | T | 1 | a0001c0006t0001g0317 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1571-24G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 10/82 | chr13 | 77262153 | ||||||
| chr13:77262289
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1571-160C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 10/82 | chr13 | 77262289 | ||||||
| chr13:77262561
|
G | C | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1571-432C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 10/82 | chr13 | 77262561 | ||||||
| chr13:77262839
|
A | T | 11 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(8): Show | 11 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1571-710T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 10/82 | chr13 | 77262839 | ||||||
| chr13:77263033
|
A | G | 1 | a0001c0004t0001g0303 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1570+618T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 10/82 | chr13 | 77263033 | ||||||
| chr13:77263362
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1570+289G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 10/82 | chr13 | 77263362 | ||||||
| chr13:77263423
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1570+228A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 10/82 | chr13 | 77263423 | ||||||
| chr13:77263431
|
A | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1570+220T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 10/82 | chr13 | 77263431 | ||||||
| chr13:77263597
|
G | A | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1570+54C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 10/82 | chr13 | 77263597 | ||||||
| chr13:77264090
|
T | G | 1 | a0001c0001t0001g0143 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1358-88A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77264090 | ||||||
| chr13:77264176
|
A | G | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1358-174T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77264176 | ||||||
| chr13:77264214
|
A | G | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1358-212T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77264214 | ||||||
| chr13:77264403
|
G | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1358-401C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77264403 | ||||||
| chr13:77264480
|
C | A | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1358-478G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77264480 | ||||||
| chr13:77264662
|
T | C | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1358-660A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77264662 | ||||||
| chr13:77264867
|
G | GCA | 28 | a0001c0002t0001g0026a0001c0003t0001g0031a0001c0003t0001g0047others(25): Show | 28 | HG00544.hp2 HG00621.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1358-867_1358-866d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77264867 | ||||||
| chr13:77264867
|
G | GCACA | 6 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358-869_1358-866d others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77264867 | ||||||
| chr13:77265159
|
T | C | 1 | a0001c0003t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1358-1157A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77265159 | ||||||
| chr13:77265503
|
A | T | 1 | a0016c0028t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1358-1501T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77265503 | ||||||
| chr13:77265552
|
A | T | 1 | a0012c0038t0002g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1358-1550T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77265552 | ||||||
| chr13:77265583
|
T | C | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1358-1581A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77265583 | ||||||
| chr13:77266065
|
G | A | 1 | a0001c0005t0002g0273 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1357+1776C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266065 | ||||||
| chr13:77266108
|
G | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1357+1733C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266108 | ||||||
| chr13:77266483
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1357+1358G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266483 | ||||||
| chr13:77266696
|
C | CATT | 20 | a0001c0001t0001g0286a0001c0001t0001g0300a0001c0003t0001g0015others(17): Show | 20 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1357+1142_1357+114 others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266696 | ||||||
| chr13:77266746
|
G | GA | 22 | a0001c0002t0001g0026a0001c0002t0001g0099a0001c0002t0001g0105others(19): Show | 22 | HG00544.hp2 HG00735.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.1357+1094dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266746 | ||||||
| chr13:77266746
|
G | GAAAAAAA | 7 | a0001c0003t0001g0031a0001c0008t0001g0302a0001c0008t0001g0305others(4): Show | 7 | HG00735.hp2 HG02145.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1357+1088_1357+109 others(11): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266746 | ||||||
| chr13:77266746
|
G | GAAAAAAA others(6): Show |
4 | a0001c0003t0001g0020a0001c0003t0001g0021a0001c0003t0001g0022others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1357+1082_1357+109 others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266746 | ||||||
| chr13:77266746
|
G | GAAAAAAA others(7): Show |
2 | a0001c0003t0001g0015a0001c0003t0001g0017 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1357+1081_1357+109 others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266746 | ||||||
| chr13:77266746
|
G | GAAAAAAA others(11): Show |
1 | a0001c0003t0001g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1357+1077_1357+109 others(22): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266746 | ||||||
| chr13:77266746
|
GA | G | 77 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 77 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1357+1094delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266746 | ||||||
| chr13:77266746
|
GAA | G | 103 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(100): Show | 103 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1357+1093_1357+109 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266746 | ||||||
| chr13:77266769
|
C | A | 7 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(4): Show | 7 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1357+1072G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266769 | ||||||
| chr13:77266772
|
T | C | 8 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(5): Show | 8 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1357+1069A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266772 | ||||||
| chr13:77266827
|
C | T | 5 | a0001c0004t0001g0265a0001c0004t0001g0266a0001c0004t0001g0267others(2): Show | 5 | HG01071.hp2 HG01261.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1357+1014G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266827 | ||||||
| chr13:77266828
|
G | A | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1357+1013C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266828 | ||||||
| chr13:77266877
|
A | G | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1357+964T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266877 | ||||||
| chr13:77266935
|
A | C | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1357+906T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77266935 | ||||||
| chr13:77267074
|
G | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1357+767C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267074 | ||||||
| chr13:77267085
|
C | T | 1 | a0001c0002t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1357+756G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267085 | ||||||
| chr13:77267323
|
T | C | 8 | a0002c0007t0001g0212a0002c0007t0001g0213a0002c0007t0001g0214others(5): Show | 8 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1357+518A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267323 | ||||||
| chr13:77267404
|
A | T | 22 | a0001c0003t0001g0044a0001c0005t0002g0078a0001c0005t0002g0079others(19): Show | 22 | HG00099.hp1 HG01928.hp1 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.1357+437T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267404 | ||||||
| chr13:77267409
|
A | T | 195 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1357+432T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267409 | ||||||
| chr13:77267414
|
T | A | 28 | a0001c0001t0001g0090a0001c0001t0001g0161a0001c0001t0001g0164others(25): Show | 28 | HG00735.hp2 HG01243.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1357+427A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267414 | ||||||
| chr13:77267419
|
T | A | 107 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(104): Show | 107 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1357+422A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267419 | ||||||
| chr13:77267424
|
T | A | 157 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0034others(154): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1357+417A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267424 | ||||||
| chr13:77267429
|
A | T | 21 | a0001c0001t0001g0144a0001c0001t0001g0225a0001c0001t0001g0230others(18): Show | 21 | HG01496.hp2 HG01981.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1357+412T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267429 | ||||||
| chr13:77267434
|
T | A | 23 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(20): Show | 23 | HG00438.hp2 HG00735.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.1357+407A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267434 | ||||||
| chr13:77267610
|
T | C | 1 | a0001c0002t0001g0103 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1357+231A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267610 | ||||||
| chr13:77267813
|
G | A | 2 | a0001c0006t0001g0324a0001c0006t0001g0325 | 2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1357+28C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 8/82 | chr13 | 77267813 | ||||||
| chr13:77267948
|
C | T | 2 | a0001c0003t0001g0260a0001c0003t0001g0261 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1261-11G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77267948 | ||||||
| chr13:77268029
|
GTACAATA others(1): Show |
G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1261-100_1261-93de others(9): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77268029 | ||||||
| chr13:77268082
|
A | G | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-145T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77268082 | ||||||
| chr13:77268131
|
A | G | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1261-194T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77268131 | ||||||
| chr13:77268417
|
C | G | 2 | a0001c0003t0001g0022a0001c0003t0001g0023 | 2 | HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1261-480G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77268417 | ||||||
| chr13:77268437
|
A | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1261-500T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77268437 | ||||||
| chr13:77268473
|
A | G | 31 | a0001c0003t0001g0129a0001c0005t0002g0078a0001c0005t0002g0079others(28): Show | 31 | HG00099.hp1 HG00621.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.1261-536T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77268473 | ||||||
| chr13:77268511
|
G | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | NA18983.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1261-574C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77268511 | ||||||
| chr13:77268694
|
G | A | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0032others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-757C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77268694 | ||||||
| chr13:77268796
|
T | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1261-859A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77268796 | ||||||
| chr13:77268962
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1261-1025A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77268962 | ||||||
| chr13:77268973
|
C | A | 1 | a0001c0021t0001g0301 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1260+1019G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77268973 | ||||||
| chr13:77269007
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1260+985G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77269007 | ||||||
| chr13:77269163
|
A | G | 2 | a0001c0004t0001g0154a0001c0004t0001g0278 | 2 | HG00408.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1260+829T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77269163 | ||||||
| chr13:77269234
|
T | C | 19 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1260+758A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77269234 | ||||||
| chr13:77269280
|
G | C | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1260+712C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77269280 | ||||||
| chr13:77269606
|
A | T | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1260+386T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77269606 | ||||||
| chr13:77269609
|
C | T | 32 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(29): Show | 32 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1260+383G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77269609 | ||||||
| chr13:77269824
|
G | T | 2 | a0001c0003t0001g0207a0001c0003t0006g0209 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1260+168C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77269824 | ||||||
| chr13:77269935
|
CA | C | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1260+56delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 7/82 | chr13 | 77269935 | ||||||
| chr13:77270073
|
A | C | 1 | a0001c0002t0001g0108 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1189-10T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 6/82 | chr13 | 77270073 | ||||||
| chr13:77270149
|
A | C | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-86T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 6/82 | chr13 | 77270149 | ||||||
| chr13:77270659
|
G | T | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.946-121C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77270659 | ||||||
| chr13:77270934
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.946-396A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77270934 | ||||||
| chr13:77271035
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.946-497G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271035 | ||||||
| chr13:77271059
|
T | C | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.946-521A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271059 | ||||||
| chr13:77271060
|
G | A | 4 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(1): Show | 4 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.946-522C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271060 | ||||||
| chr13:77271082
|
A | C | 326 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.946-544T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271082 | ||||||
| chr13:77271328
|
C | T | 1 | a0001c0002t0001g0059 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.946-790G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271328 | ||||||
| chr13:77271496
|
G | C | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.946-958C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271496 | ||||||
| chr13:77271504
|
TC | T | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-967delG | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271504 | ||||||
| chr13:77271692
|
A | G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.946-1154T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271692 | ||||||
| chr13:77271696
|
G | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.946-1158C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271696 | ||||||
| chr13:77271798
|
G | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.946-1260C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271798 | ||||||
| chr13:77271880
|
G | C | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.946-1342C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271880 | ||||||
| chr13:77271959
|
G | A | 3 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0203 | 3 | HG02027.hp1 NA18947.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.946-1421C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271959 | ||||||
| chr13:77271968
|
T | A | 1 | a0001c0014t0001g0050 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.946-1430A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77271968 | ||||||
| chr13:77272001
|
A | T | 86 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(83): Show | 87 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.946-1463T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77272001 | ||||||
| chr13:77272349
|
G | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.945+1123C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77272349 | ||||||
| chr13:77272487
|
G | A | 1 | a0001c0020t0001g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.945+985C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77272487 | ||||||
| chr13:77272722
|
G | T | 1 | a0001c0002t0001g0114 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.945+750C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77272722 | ||||||
| chr13:77272818
|
C | G | 1 | a0001c0023t0001g0206 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.945+654G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77272818 | ||||||
| chr13:77272859
|
T | A | 3 | a0001c0003t0001g0044a0001c0003t0001g0096a0001c0033t0001g0045 | 3 | HG02647.hp2 HG02896.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.945+613A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77272859 | ||||||
| chr13:77273082
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.945+390T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77273082 | ||||||
| chr13:77273089
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.945+383A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77273089 | ||||||
| chr13:77273400
|
A | T | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.945+72T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77273400 | ||||||
| chr13:77273462
|
T | C | 2 | a0001c0002t0001g0048a0001c0002t0001g0067 | 2 | NA18979.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.945+10A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 5/82 | chr13 | 77273462 | ||||||
| chr13:77273709
|
C | T | 1 | a0001c0002t0001g0039 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.749-41G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77273709 | ||||||
| chr13:77273796
|
A | G | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.749-128T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77273796 | ||||||
| chr13:77273974
|
G | C | 35 | a0001c0002t0001g0001a0001c0002t0001g0099a0001c0002t0001g0100others(32): Show | 36 | HG00597.hp2 HG00673.hp1 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.749-306C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77273974 | ||||||
| chr13:77273990
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.749-322A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77273990 | ||||||
| chr13:77274228
|
T | G | 330 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.749-560A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77274228 | ||||||
| chr13:77274398
|
C | A | 1 | a0001c0005t0002g0222 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.749-730G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77274398 | ||||||
| chr13:77274698
|
T | G | 1 | a0001c0006t0001g0321 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.749-1030A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77274698 | ||||||
| chr13:77274841
|
T | C | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.749-1173A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77274841 | ||||||
| chr13:77275048
|
A | G | 1 | a0001c0006t0001g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.749-1380T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77275048 | ||||||
| chr13:77275140
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.749-1472G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77275140 | ||||||
| chr13:77275177
|
AAT | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.749-1511_749-1510d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77275177 | ||||||
| chr13:77275460
|
T | C | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.749-1792A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77275460 | ||||||
| chr13:77275508
|
A | G | 1 | a0001c0003t0001g0020 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.749-1840T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77275508 | ||||||
| chr13:77275543
|
G | C | 104 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(101): Show | 105 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.749-1875C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77275543 | ||||||
| chr13:77275678
|
T | A | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.749-2010A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77275678 | ||||||
| chr13:77275706
|
A | G | 11 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG02027.hp2 HG02071.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.749-2038T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77275706 | ||||||
| chr13:77275710
|
G | A | 1 | a0001c0004t0001g0088 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.749-2042C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77275710 | ||||||
| chr13:77275901
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.749-2233A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77275901 | ||||||
| chr13:77276030
|
C | T | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | NA18954.hp2 NA18964.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-2362G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276030 | ||||||
| chr13:77276031
|
G | A | 10 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(7): Show | 10 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.749-2363C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276031 | ||||||
| chr13:77276035
|
T | C | 1 | a0001c0002t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.749-2367A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276035 | ||||||
| chr13:77276120
|
A | C | 2 | a0001c0004t0001g0153a0001c0004t0001g0240 | 2 | NA18946.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.749-2452T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276120 | ||||||
| chr13:77276339
|
C | T | 1 | a0001c0019t0001g0274 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.748+2419G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276339 | ||||||
| chr13:77276386
|
A | C | 1 | a0001c0021t0001g0301 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.748+2372T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276386 | ||||||
| chr13:77276661
|
T | TG | 6 | a0001c0001t0001g0172a0001c0003t0001g0047a0001c0003t0001g0097others(3): Show | 6 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.748+2096dupC | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276661 | ||||||
| chr13:77276666
|
G | T | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.748+2092C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276666 | ||||||
| chr13:77276667
|
T | G | 204 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.748+2091A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276667 | ||||||
| chr13:77276669
|
T | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.748+2089A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276669 | ||||||
| chr13:77276769
|
C | T | 1 | a0001c0045t0001g0327 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.748+1989G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276769 | ||||||
| chr13:77276770
|
G | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.748+1988C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276770 | ||||||
| chr13:77276816
|
G | GT | 140 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(137): Show | 140 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.748+1941dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276816 | ||||||
| chr13:77276816
|
G | GTT | 17 | a0001c0001t0001g0008a0001c0001t0001g0090a0001c0001t0001g0158others(14): Show | 17 | HG00621.hp2 HG01109.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.748+1940_748+1941d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276816 | ||||||
| chr13:77276816
|
G | GTTT | 6 | a0001c0003t0001g0015a0001c0003t0001g0017a0001c0003t0001g0020others(3): Show | 6 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.748+1939_748+1941d others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276816 | ||||||
| chr13:77276816
|
G | GTTTTTTT others(5): Show |
4 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0305others(1): Show | 4 | HG02109.hp2 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.748+1930_748+1941d others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276816 | ||||||
| chr13:77276816
|
G | GTTTTTTT others(6): Show |
4 | a0001c0003t0001g0031a0001c0008t0001g0302a0001c0008t0001g0307others(1): Show | 4 | HG02145.hp1 HG03139.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.748+1929_748+1941d others(15): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276816 | ||||||
| chr13:77276816
|
G | GTTTTTTT others(7): Show |
1 | a0001c0008t0001g0306 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.748+1928_748+1941d others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276816 | ||||||
| chr13:77276816
|
GT | G | 111 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0036others(108): Show | 112 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.748+1941delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276816 | ||||||
| chr13:77276841
|
G | T | 19 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.748+1917C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276841 | ||||||
| chr13:77276862
|
C | T | 156 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(153): Show | 156 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.748+1896G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77276862 | ||||||
| chr13:77277043
|
G | A | 9 | a0002c0007t0001g0212a0002c0007t0001g0213a0002c0007t0001g0214others(6): Show | 9 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.748+1715C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77277043 | ||||||
| chr13:77277450
|
A | G | 1 | a0005c0015t0001g0258 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.748+1308T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77277450 | ||||||
| chr13:77277558
|
G | A | 19 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.748+1200C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77277558 | ||||||
| chr13:77277569
|
A | ACAGGTGG others(12): Show |
1 | a0001c0002t0001g0200 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.748+1170_748+1188d others(21): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77277569 | ||||||
| chr13:77277604
|
G | A | 1 | a0001c0003t0001g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.748+1154C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77277604 | ||||||
| chr13:77277644
|
C | G | 330 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.748+1114G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77277644 | ||||||
| chr13:77277774
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.748+984A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77277774 | ||||||
| chr13:77278199
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.748+559A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77278199 | ||||||
| chr13:77278348
|
C | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.748+410G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77278348 | ||||||
| chr13:77278458
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.748+300G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77278458 | ||||||
| chr13:77278542
|
T | C | 2 | a0001c0002t0001g0102a0001c0002t0001g0149 | 2 | HG02165.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.748+216A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77278542 | ||||||
| chr13:77278721
|
C | T | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.748+37G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 4/82 | chr13 | 77278721 | ||||||
| chr13:77279220
|
T | C | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.595-309A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77279220 | ||||||
| chr13:77279236
|
C | T | 330 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.595-325G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77279236 | ||||||
| chr13:77279249
|
G | A | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.595-338C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77279249 | ||||||
| chr13:77279270
|
G | C | 1 | a0006c0017t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.595-359C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77279270 | ||||||
| chr13:77279607
|
T | C | 19 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(16): Show | 19 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.595-696A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77279607 | ||||||
| chr13:77279742
|
T | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.595-831A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77279742 | ||||||
| chr13:77279926
|
A | G | 10 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(7): Show | 10 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.595-1015T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77279926 | ||||||
| chr13:77279949
|
C | T | 1 | a0001c0008t0001g0307 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.595-1038G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77279949 | ||||||
| chr13:77279992
|
G | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.595-1081C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77279992 | ||||||
| chr13:77279998
|
A | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.595-1087T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77279998 | ||||||
| chr13:77280018
|
A | G | 41 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 41 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.595-1107T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77280018 | ||||||
| chr13:77280088
|
C | T | 1 | a0001c0002t0001g0060 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.595-1177G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77280088 | ||||||
| chr13:77280109
|
T | C | 10 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(7): Show | 10 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.595-1198A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77280109 | ||||||
| chr13:77280151
|
T | C | 1 | a0001c0001t0001g0238 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.595-1240A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77280151 | ||||||
| chr13:77280389
|
A | T | 2 | a0001c0006t0001g0328a0001c0006t0001g0329 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.595-1478T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77280389 | ||||||
| chr13:77280503
|
T | C | 330 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.595-1592A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77280503 | ||||||
| chr13:77280903
|
A | C | 1 | a0001c0002t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.595-1992T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77280903 | ||||||
| chr13:77280987
|
A | G | 1 | a0002c0040t0001g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.595-2076T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77280987 | ||||||
| chr13:77281136
|
A | C | 1 | a0001c0003t0001g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.595-2225T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77281136 | ||||||
| chr13:77281201
|
C | T | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.595-2290G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77281201 | ||||||
| chr13:77281358
|
T | G | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.595-2447A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77281358 | ||||||
| chr13:77281380
|
T | C | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.595-2469A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77281380 | ||||||
| chr13:77281510
|
C | T | 1 | a0001c0009t0001g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.595-2599G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77281510 | ||||||
| chr13:77281629
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.595-2718C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77281629 | ||||||
| chr13:77281786
|
CTAAG | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0169a0001c0001t0001g0177others(2): Show | 5 | HG02165.hp2 NA18974.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-2879_595-2876d others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77281786 | ||||||
| chr13:77281924
|
G | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.595-3013C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77281924 | ||||||
| chr13:77282102
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.595-3191C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77282102 | ||||||
| chr13:77282179
|
G | A | 1 | a0001c0003t0001g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.595-3268C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77282179 | ||||||
| chr13:77282279
|
G | A | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.595-3368C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77282279 | ||||||
| chr13:77282411
|
GA | G | 37 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(34): Show | 37 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.595-3501delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77282411 | ||||||
| chr13:77282636
|
T | G | 2 | a0001c0006t0001g0328a0001c0006t0001g0329 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.595-3725A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77282636 | ||||||
| chr13:77282829
|
A | G | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-3918T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77282829 | ||||||
| chr13:77282940
|
T | C | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.595-4029A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77282940 | ||||||
| chr13:77283154
|
C | T | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.595-4243G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77283154 | ||||||
| chr13:77283324
|
C | T | 1 | a0001c0003t0001g0210 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.595-4413G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77283324 | ||||||
| chr13:77283625
|
G | A | 1 | a0001c0003t0001g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.594+4536C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77283625 | ||||||
| chr13:77283696
|
A | G | 1 | a0001c0004t0001g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.594+4465T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77283696 | ||||||
| chr13:77283866
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.594+4295G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77283866 | ||||||
| chr13:77283964
|
T | A | 1 | a0001c0001t0001g0182 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.594+4197A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77283964 | ||||||
| chr13:77284139
|
T | G | 6 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.594+4022A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284139 | ||||||
| chr13:77284170
|
G | A | 1 | a0001c0004t0001g0240 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.594+3991C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284170 | ||||||
| chr13:77284256
|
A | G | 330 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.594+3905T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284256 | ||||||
| chr13:77284260
|
A | G | 163 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.594+3901T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284260 | ||||||
| chr13:77284290
|
C | T | 25 | a0001c0001t0001g0280a0001c0004t0001g0087a0001c0004t0001g0088others(22): Show | 25 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.594+3871G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284290 | ||||||
| chr13:77284311
|
C | A | 1 | a0001c0001t0003g0005 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.594+3850G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284311 | ||||||
| chr13:77284334
|
G | A | 1 | a0001c0044t0001g0332 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.594+3827C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284334 | ||||||
| chr13:77284340
|
T | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+3821A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284340 | ||||||
| chr13:77284348
|
T | C | 114 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(111): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.594+3813A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284348 | ||||||
| chr13:77284378
|
G | C | 112 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.594+3783C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284378 | ||||||
| chr13:77284753
|
C | T | 3 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0137 | 3 | NA18966.hp2 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.594+3408G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284753 | ||||||
| chr13:77284759
|
C | G | 2 | a0001c0002t0001g0001a0001c0002t0001g0114 | 3 | HG03490.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.594+3402G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284759 | ||||||
| chr13:77284833
|
T | G | 1 | a0001c0002t0001g0026 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.594+3328A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77284833 | ||||||
| chr13:77285103
|
C | T | 1 | a0001c0004t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.594+3058G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285103 | ||||||
| chr13:77285163
|
G | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+2998C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285163 | ||||||
| chr13:77285648
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.594+2513G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285648 | ||||||
| chr13:77285810
|
C | G | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.594+2351G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285810 | ||||||
| chr13:77285857
|
G | GGGAAA | 12 | a0001c0003t0001g0014a0001c0003t0001g0041a0001c0003t0001g0042others(9): Show | 12 | HG02559.hp2 HG02572.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.594+2299_594+2303d others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285857 | ||||||
| chr13:77285857
|
G | GGGAAAGG others(3): Show |
41 | a0001c0002t0001g0025a0001c0002t0001g0048a0001c0002t0001g0049others(38): Show | 41 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.594+2294_594+2303d others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285857 | ||||||
| chr13:77285857
|
G | GGGAAAGG others(8): Show |
25 | a0001c0002t0001g0026a0001c0002t0001g0036a0001c0002t0001g0039others(22): Show | 25 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.594+2289_594+2303d others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285857 | ||||||
| chr13:77285857
|
G | GGGAAAGG others(13): Show |
24 | a0001c0002t0001g0001a0001c0002t0001g0101a0001c0002t0001g0103others(21): Show | 25 | HG00673.hp1 HG01981.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.594+2284_594+2303d others(22): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285857 | ||||||
| chr13:77285857
|
G | GGGAAAGG others(18): Show |
7 | a0001c0002t0001g0099a0001c0002t0001g0100a0001c0002t0001g0105others(4): Show | 7 | HG02647.hp1 HG04199.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.594+2279_594+2303d others(27): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285857 | ||||||
| chr13:77285857
|
G | GGGAAC | 4 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(1): Show | 4 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+2303_594+2304i others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285857 | ||||||
| chr13:77285857
|
GGGAAA | G | 7 | a0001c0003t0001g0072a0001c0003t0001g0260a0001c0003t0001g0261others(4): Show | 7 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.594+2299_594+2303d others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285857 | ||||||
| chr13:77285857
|
GGGAAAGG others(3): Show |
G | 74 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(71): Show | 74 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.594+2294_594+2303d others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285857 | ||||||
| chr13:77285857
|
GGGAAAGG others(8): Show |
G | 123 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(120): Show | 123 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.594+2289_594+2303d others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285857 | ||||||
| chr13:77285857
|
GGGAAAGG others(13): Show |
G | 1 | a0001c0003t0001g0071 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.594+2284_594+2303d others(22): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285857 | ||||||
| chr13:77285862
|
A | C | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.594+2299T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285862 | ||||||
| chr13:77285874
|
GAAAGGAA others(18): Show |
G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.594+2262_594+2286d others(27): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285874 | ||||||
| chr13:77285884
|
GAAAGGAA others(8): Show |
G | 9 | a0001c0003t0001g0031a0001c0008t0001g0263a0001c0008t0001g0296others(6): Show | 9 | HG00735.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.594+2262_594+2276d others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285884 | ||||||
| chr13:77285889
|
G | GAAAGGAA others(13): Show |
1 | a0001c0002t0001g0205 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.594+2271_594+2272i others(22): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285889 | ||||||
| chr13:77285921
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.594+2240C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285921 | ||||||
| chr13:77285932
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.594+2229A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285932 | ||||||
| chr13:77285987
|
G | T | 31 | a0001c0003t0001g0129a0001c0005t0002g0078a0001c0005t0002g0079others(28): Show | 31 | HG00099.hp1 HG00621.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.594+2174C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77285987 | ||||||
| chr13:77286341
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+1820T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286341 | ||||||
| chr13:77286344
|
G | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+1817C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286344 | ||||||
| chr13:77286454
|
G | A | 41 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 41 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.594+1707C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286454 | ||||||
| chr13:77286755
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0013 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.594+1396_594+1405d others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286755 | ||||||
| chr13:77286755
|
CA | C | 12 | a0001c0001t0001g0094a0001c0001t0001g0179a0001c0001t0001g0232others(9): Show | 12 | HG00438.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.594+1405delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286755 | ||||||
| chr13:77286755
|
CAA | C | 16 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0139others(13): Show | 16 | HG00621.hp1 HG01106.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.594+1404_594+1405d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286755 | ||||||
| chr13:77286755
|
CAAA | C | 21 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0141others(18): Show | 22 | HG00408.hp1 HG01516.hp2 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.594+1403_594+1405d others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286755 | ||||||
| chr13:77286755
|
CAAAA | C | 16 | a0001c0002t0001g0064a0001c0002t0001g0100a0001c0002t0001g0103others(13): Show | 16 | HG00673.hp1 HG02015.hp1 HG04184.hp2 others(13): Show |
intron_variant | MODIFIER | c.594+1402_594+1405d others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286755 | ||||||
| chr13:77286755
|
CAAAAAAA | C | 7 | a0001c0002t0001g0039a0001c0002t0001g0059a0001c0002t0001g0066others(4): Show | 7 | HG00558.hp1 HG01099.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.594+1399_594+1405d others(9): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286755 | ||||||
| chr13:77286755
|
CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0001g0011a0001c0002t0001g0049a0001c0006t0001g0323others(5): Show | 8 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+1398_594+1405d others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286755 | ||||||
| chr13:77286755
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0004t0001g0153a0001c0004t0001g0240a0001c0004t0001g0243 | 3 | NA18946.hp2 NA18947.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.594+1394_594+1405d others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286755 | ||||||
| chr13:77286755
|
CAAAAAAA others(7): Show |
C | 6 | a0001c0004t0001g0087a0001c0004t0001g0150a0001c0004t0001g0242others(3): Show | 6 | HG00621.hp2 NA18971.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.594+1392_594+1405d others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286755 | ||||||
| chr13:77286755
|
CAAAAAAA others(8): Show |
C | 9 | a0001c0004t0001g0088a0001c0004t0001g0151a0001c0004t0001g0154others(6): Show | 9 | HG00408.hp2 HG00558.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.594+1391_594+1405d others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286755 | ||||||
| chr13:77286756
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.594+1405T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286756 | ||||||
| chr13:77286774
|
AAAAAAAA others(10): Show |
A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.594+1370_594+1386d others(19): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286774 | ||||||
| chr13:77286775
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0004t0001g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.594+1370_594+1385d others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286775 | ||||||
| chr13:77286776
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0280 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.594+1370_594+1384d others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286776 | ||||||
| chr13:77286777
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.594+1383_594+1384i others(15): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286777 | ||||||
| chr13:77286779
|
A | T | 1 | a0001c0001t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.594+1382T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286779 | ||||||
| chr13:77286781
|
A | AATATATA others(3): Show |
1 | a0001c0005t0002g0268 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.594+1379_594+1380i others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286781 | ||||||
| chr13:77286781
|
A | T | 1 | a0001c0001t0001g0312 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.594+1380T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286781 | ||||||
| chr13:77286783
|
A | AAT | 8 | a0001c0001t0001g0034a0001c0001t0001g0089a0001c0001t0001g0168others(5): Show | 8 | HG00609.hp1 HG01255.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+1377_594+1378i others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286783 | ||||||
| chr13:77286783
|
A | AT | 6 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0177others(3): Show | 6 | HG01928.hp2 NA18955.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.594+1377_594+1378i others(3): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286783 | ||||||
| chr13:77286783
|
A | ATAT | 3 | a0001c0001t0001g0007a0001c0001t0001g0190a0001c0036t0001g0291 | 3 | HG02055.hp1 NA18961.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.594+1377_594+1378i others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286783 | ||||||
| chr13:77286783
|
A | ATATATAT others(6): Show |
1 | a0001c0005t0002g0269 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.594+1377_594+1378i others(15): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286783 | ||||||
| chr13:77286783
|
A | T | 7 | a0001c0001t0001g0262a0001c0001t0001g0312a0001c0001t0001g0313others(4): Show | 7 | HG02015.hp2 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.594+1378T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286783 | ||||||
| chr13:77286783
|
AAAAAAAA others(1): Show |
A | 7 | a0001c0002t0001g0052a0001c0002t0001g0054a0001c0002t0001g0055others(4): Show | 7 | HG00609.hp2 HG01168.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.594+1370_594+1377d others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286783 | ||||||
| chr13:77286784
|
AAAAAAAT | A | 8 | a0001c0002t0001g0036a0001c0002t0001g0048a0001c0002t0001g0056others(5): Show | 8 | HG00280.hp1 HG00642.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.594+1370_594+1376d others(9): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286784 | ||||||
| chr13:77286785
|
A | AAT | 7 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0195others(4): Show | 7 | HG00673.hp2 HG01934.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.594+1375_594+1376i others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286785 | ||||||
| chr13:77286785
|
A | AATATATA others(3): Show |
1 | a0001c0005t0002g0221 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.594+1375_594+1376i others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286785 | ||||||
| chr13:77286785
|
A | AATATATA others(5): Show |
1 | a0001c0013t0001g0192 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.594+1375_594+1376i others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286785 | ||||||
| chr13:77286785
|
A | AATATATA others(7): Show |
1 | a0001c0005t0002g0271 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.594+1375_594+1376i others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286785 | ||||||
| chr13:77286785
|
A | AATATATA others(23): Show |
1 | a0001c0008t0001g0302 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.594+1375_594+1376i others(32): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286785 | ||||||
| chr13:77286785
|
A | AT | 8 | a0001c0001t0001g0130a0001c0001t0001g0163a0001c0001t0001g0188others(5): Show | 8 | HG00438.hp1 HG01167.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.594+1375_594+1376i others(3): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286785 | ||||||
| chr13:77286785
|
A | ATAT | 5 | a0001c0001t0001g0186a0001c0001t0001g0286a0001c0001t0001g0290others(2): Show | 5 | HG00544.hp1 HG02897.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+1375_594+1376i others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286785 | ||||||
| chr13:77286785
|
A | ATATATAT others(4): Show |
3 | a0001c0005t0002g0138a0001c0005t0002g0270a0001c0013t0001g0191 | 3 | HG00099.hp1 NA18968.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.594+1375_594+1376i others(13): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286785 | ||||||
| chr13:77286785
|
A | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0089others(37): Show | 40 | HG00597.hp1 HG00609.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.594+1376T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286785 | ||||||
| chr13:77286785
|
AAAAAAT | A | 7 | a0001c0002t0001g0026a0001c0002t0001g0057a0001c0002t0001g0062others(4): Show | 7 | HG00544.hp2 HG01099.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.594+1370_594+1375d others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286785 | ||||||
| chr13:77286785
|
AAAAAATA others(11): Show |
A | 1 | a0007c0018t0003g0004 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.594+1358_594+1375d others(20): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286785 | ||||||
| chr13:77286787
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0095 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.594+1373_594+1374i others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | AATATATA others(5): Show |
3 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0137 | 3 | NA18966.hp2 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.594+1373_594+1374i others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | AATATATA others(25): Show |
1 | a0001c0001t0001g0276 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.594+1373_594+1374i others(34): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | AT | 4 | a0001c0001t0001g0159a0001c0001t0001g0248a0001c0001t0001g0298others(1): Show | 4 | NA19001.hp1 NA19054.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+1373_594+1374i others(3): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | ATAT | 4 | a0001c0001t0001g0093a0001c0001t0001g0249a0001c0009t0001g0077others(1): Show | 4 | HG00423.hp2 HG01515.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+1373_594+1374i others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | ATATAT | 3 | a0001c0001t0001g0164a0002c0007t0001g0214a0002c0007t0001g0216 | 3 | HG02896.hp2 HG02897.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.594+1373_594+1374i others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | ATATATAT others(4): Show |
4 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(1): Show | 4 | NA18946.hp1 NA18978.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+1373_594+1374i others(13): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | ATATATAT others(6): Show |
1 | a0001c0005t0002g0223 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.594+1373_594+1374i others(15): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | ATATATAT others(8): Show |
1 | a0013c0037t0002g0134 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.594+1373_594+1374i others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0315 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.594+1373_594+1374i others(21): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0238 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.594+1373_594+1374i others(25): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.594+1373_594+1374i others(27): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | ATATATAT others(28): Show |
1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.594+1373_594+1374i others(37): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
A | T | 103 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.594+1374T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286787
|
AAAATATA others(9): Show |
A | 1 | a0001c0001t0003g0002 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.594+1358_594+1373d others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286787 | ||||||
| chr13:77286788
|
A | ATATATAT others(26): Show |
1 | a0001c0003t0001g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.594+1372_594+1373i others(35): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286788 | ||||||
| chr13:77286789
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.594+1371_594+1372i others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAAAAAAA others(35): Show |
1 | a0001c0008t0001g0306 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.594+1371_594+1372i others(44): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.594+1371_594+1372i others(13): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAAAAATA others(9): Show |
1 | a0001c0008t0001g0308 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.594+1371_594+1372i others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAAAATAT others(12): Show |
1 | a0001c0008t0001g0307 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.594+1371_594+1372i others(21): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAAATATA others(3): Show |
2 | a0001c0003t0001g0018a0001c0003t0001g0019 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.594+1371_594+1372i others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAAATATA others(7): Show |
1 | a0001c0008t0001g0305 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.594+1371_594+1372i others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAAATATA others(9): Show |
1 | a0001c0008t0001g0263 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.594+1371_594+1372i others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAAATATA others(11): Show |
1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.594+1371_594+1372i others(20): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAATATAT others(4): Show |
1 | a0001c0005t0002g0273 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.594+1371_594+1372i others(13): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAATATAT others(8): Show |
1 | a0012c0038t0002g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.594+1371_594+1372i others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAATATAT others(12): Show |
1 | a0001c0019t0001g0274 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.594+1371_594+1372i others(21): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAATATAT others(14): Show |
1 | a0001c0001t0001g0146 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.594+1371_594+1372i others(23): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AAATATAT others(20): Show |
1 | a0001c0001t0001g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.594+1371_594+1372i others(29): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AATATATA others(9): Show |
1 | a0001c0008t0001g0296 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.594+1356_594+1371d others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AATATATA others(13): Show |
1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.594+1352_594+1371d others(22): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | AATATATA others(19): Show |
1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.594+1346_594+1371d others(28): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | ATATATAT others(4): Show |
2 | a0001c0005t0002g0136a0001c0005t0002g0272 | 2 | NA18981.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.594+1371_594+1372i others(13): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | ATATATAT others(6): Show |
1 | a0001c0008t0001g0309 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.594+1371_594+1372i others(15): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0314 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.594+1371_594+1372i others(25): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0003g0005 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.594+1371_594+1372i others(27): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0275 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.594+1371_594+1372i others(29): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286789
|
A | T | 179 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.594+1372T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286789 | ||||||
| chr13:77286790
|
A | G | 1 | a0001c0003t0001g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.594+1371T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286790 | ||||||
| chr13:77286790
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0003g0003 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.594+1356_594+1370d others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286790 | ||||||
| chr13:77286793
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.594+1368A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286793 | ||||||
| chr13:77286796
|
A | G | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.594+1365T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286796 | ||||||
| chr13:77286797
|
T | A | 1 | a0001c0003t0001g0289 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.594+1364A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286797 | ||||||
| chr13:77286936
|
G | C | 3 | a0001c0005t0002g0268a0001c0005t0002g0269a0001c0005t0002g0270 | 3 | NA18982.hp1 NA18983.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.594+1225C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286936 | ||||||
| chr13:77286953
|
C | T | 41 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 41 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.594+1208G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77286953 | ||||||
| chr13:77287063
|
G | A | 114 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(111): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.594+1098C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287063 | ||||||
| chr13:77287094
|
A | T | 1 | a0001c0002t0001g0100 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.594+1067T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287094 | ||||||
| chr13:77287130
|
G | A | 2 | a0001c0002t0001g0121a0001c0002t0001g0122 | 2 | NA19085.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.594+1031C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287130 | ||||||
| chr13:77287138
|
T | C | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+1023A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287138 | ||||||
| chr13:77287167
|
G | A | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+994C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287167 | ||||||
| chr13:77287192
|
C | CT | 83 | a0001c0001t0001g0233a0001c0002t0001g0025a0001c0002t0001g0026others(80): Show | 83 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.594+968dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287192 | ||||||
| chr13:77287244
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0251 | 2 | HG00738.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.594+917C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287244 | ||||||
| chr13:77287326
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.594+835T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287326 | ||||||
| chr13:77287354
|
T | C | 114 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(111): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.594+807A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287354 | ||||||
| chr13:77287596
|
T | C | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+565A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287596 | ||||||
| chr13:77287696
|
C | G | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.594+465G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287696 | ||||||
| chr13:77287743
|
A | C | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.594+418T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287743 | ||||||
| chr13:77287940
|
G | A | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.594+221C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77287940 | ||||||
| chr13:77288091
|
G | A | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.594+70C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77288091 | ||||||
| chr13:77288136
|
A | G | 1 | a0001c0004t0001g0265 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.594+25T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 3/82 | chr13 | 77288136 | ||||||
| chr13:77288536
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-160G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77288536 | ||||||
| chr13:77288547
|
C | G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.379-171G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77288547 | ||||||
| chr13:77288602
|
A | T | 5 | a0001c0001t0001g0163a0001c0001t0001g0173a0001c0001t0001g0249others(2): Show | 5 | HG00738.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-226T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77288602 | ||||||
| chr13:77288849
|
G | A | 211 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.379-473C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77288849 | ||||||
| chr13:77288900
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.379-524G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77288900 | ||||||
| chr13:77289390
|
C | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0255 | 2 | NA18943.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.379-1014G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77289390 | ||||||
| chr13:77289475
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.379-1099T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77289475 | ||||||
| chr13:77289638
|
G | A | 1 | a0001c0004t0001g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.379-1262C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77289638 | ||||||
| chr13:77289694
|
G | A | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.379-1318C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77289694 | ||||||
| chr13:77289774
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.379-1398T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77289774 | ||||||
| chr13:77289862
|
TA | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-1487delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77289862 | ||||||
| chr13:77290371
|
C | T | 1 | a0001c0006t0001g0321 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.379-1995G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77290371 | ||||||
| chr13:77290712
|
G | A | 32 | a0001c0001t0001g0007a0001c0001t0001g0095a0001c0001t0001g0159others(29): Show | 32 | HG00544.hp1 HG00609.hp1 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.379-2336C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77290712 | ||||||
| chr13:77290754
|
C | T | 111 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(108): Show | 111 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.379-2378G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77290754 | ||||||
| chr13:77291054
|
T | C | 9 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(6): Show | 9 | HG01071.hp2 HG01261.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.379-2678A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77291054 | ||||||
| chr13:77291102
|
G | A | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.379-2726C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77291102 | ||||||
| chr13:77291192
|
G | C | 1 | a0001c0002t0001g0062 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.379-2816C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77291192 | ||||||
| chr13:77291244
|
C | A | 27 | a0001c0001t0001g0280a0001c0004t0001g0087a0001c0004t0001g0088others(24): Show | 27 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.379-2868G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77291244 | ||||||
| chr13:77291337
|
C | T | 1 | a0001c0006t0001g0318 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.379-2961G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77291337 | ||||||
| chr13:77291463
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.379-3087A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77291463 | ||||||
| chr13:77291639
|
T | C | 1 | a0001c0006t0001g0319 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.379-3263A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77291639 | ||||||
| chr13:77291661
|
G | A | 1 | a0001c0003t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.379-3285C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77291661 | ||||||
| chr13:77291977
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-3601A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77291977 | ||||||
| chr13:77292003
|
G | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-3627C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292003 | ||||||
| chr13:77292077
|
T | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-3701A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292077 | ||||||
| chr13:77292136
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.379-3760A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292136 | ||||||
| chr13:77292349
|
A | C | 4 | a0001c0002t0001g0056a0001c0002t0001g0057a0001c0002t0001g0062others(1): Show | 4 | HG00423.hp1 NA18978.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-3973T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292349 | ||||||
| chr13:77292527
|
A | C | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.378+4072T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292527 | ||||||
| chr13:77292530
|
T | TA | 114 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(111): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.378+4068dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292530 | ||||||
| chr13:77292531
|
A | T | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+4068T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292531 | ||||||
| chr13:77292696
|
T | C | 123 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(120): Show | 123 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.378+3903A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292696 | ||||||
| chr13:77292811
|
A | G | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+3788T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292811 | ||||||
| chr13:77292819
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.378+3780C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292819 | ||||||
| chr13:77292911
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.378+3688G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292911 | ||||||
| chr13:77292954
|
G | A | 1 | a0001c0002t0001g0124 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.378+3645C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292954 | ||||||
| chr13:77292958
|
C | CA | 18 | a0001c0001t0001g0163a0001c0002t0001g0055a0001c0002t0001g0068others(15): Show | 18 | HG00673.hp1 HG00735.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.378+3640dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292958 | ||||||
| chr13:77292958
|
C | CAA | 52 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.378+3639_378+3640d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292958 | ||||||
| chr13:77292958
|
C | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+3641G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292958 | ||||||
| chr13:77292974
|
A | G | 13 | a0001c0003t0001g0014a0001c0003t0001g0028a0001c0003t0001g0029others(10): Show | 13 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.378+3625T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77292974 | ||||||
| chr13:77293135
|
C | T | 10 | a0001c0001t0001g0140a0001c0008t0001g0263a0001c0008t0001g0296others(7): Show | 10 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.378+3464G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77293135 | ||||||
| chr13:77293637
|
T | C | 1 | a0001c0001t0001g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.378+2962A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77293637 | ||||||
| chr13:77293779
|
G | C | 1 | a0001c0023t0001g0206 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.378+2820C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77293779 | ||||||
| chr13:77293993
|
A | C | 114 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(111): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.378+2606T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77293993 | ||||||
| chr13:77294102
|
G | A | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.378+2497C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294102 | ||||||
| chr13:77294104
|
C | A | 1 | a0002c0007t0001g0219 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.378+2495G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTA | 4 | a0001c0002t0001g0201a0001c0003t0001g0260a0001c0003t0001g0261others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+2493_378+2494d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTATATA | 7 | a0001c0002t0001g0036a0001c0002t0001g0103a0001c0002t0001g0104others(4): Show | 7 | HG00280.hp1 HG02004.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+2489_378+2494d others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTATATAT others(1): Show |
8 | a0001c0002t0001g0060a0001c0002t0001g0067a0001c0002t0001g0068others(5): Show | 8 | HG01099.hp1 HG01256.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.378+2487_378+2494d others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTATATAT others(3): Show |
43 | a0001c0002t0001g0001a0001c0002t0001g0026a0001c0002t0001g0039others(40): Show | 44 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.378+2485_378+2494d others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTATATAT others(5): Show |
30 | a0001c0002t0001g0052a0001c0002t0001g0054a0001c0002t0001g0055others(27): Show | 30 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.378+2483_378+2494d others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTATATAT others(7): Show |
6 | a0001c0002t0001g0108a0001c0002t0001g0114a0001c0002t0001g0123others(3): Show | 6 | HG02109.hp1 HG04199.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+2481_378+2494d others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTATATAT others(9): Show |
8 | a0001c0002t0001g0048a0001c0002t0001g0125a0001c0002t0001g0203others(5): Show | 8 | HG01981.hp2 HG02027.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+2479_378+2494d others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTATATAT others(11): Show |
14 | a0001c0005t0002g0131a0001c0005t0002g0132a0001c0005t0002g0133others(11): Show | 14 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.378+2494_378+2495i others(20): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTATATAT others(17): Show |
1 | a0001c0005t0002g0272 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.378+2494_378+2495i others(26): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTATATAT others(11): Show |
3 | a0001c0001t0001g0158a0001c0002t0001g0115a0001c0006t0001g0321 | 3 | HG01168.hp1 HG01884.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.378+2477_378+2494d others(20): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTATATAT others(31): Show |
1 | a0001c0002t0001g0199 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.378+2494_378+2495i others(40): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294104
|
C | CTATATAT others(37): Show |
1 | a0018c0042t0001g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.378+2494_378+2495i others(46): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294104 | ||||||
| chr13:77294105
|
T | TATATATA others(7): Show |
2 | a0001c0001t0004g0181a0001c0001t0004g0184 | 2 | NA18942.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.378+2493_378+2494i others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294105 | ||||||
| chr13:77294105
|
T | TATATATA others(9): Show |
3 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0137 | 3 | NA18966.hp2 NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.378+2493_378+2494i others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294105 | ||||||
| chr13:77294107
|
T | TATATATA others(21): Show |
3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG01167.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.378+2491_378+2492i others(30): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294107 | ||||||
| chr13:77294107
|
T | TATATATA others(23): Show |
1 | a0001c0001t0001g0254 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.378+2491_378+2492i others(32): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294107 | ||||||
| chr13:77294110
|
A | ATATATAT others(7): Show |
1 | a0001c0009t0001g0076 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.378+2488_378+2489i others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294110 | ||||||
| chr13:77294110
|
A | ATATATAT others(3): Show |
1 | a0001c0009t0001g0311 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.378+2488_378+2489i others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294110 | ||||||
| chr13:77294111
|
T | TATATACA others(25): Show |
1 | a0001c0001t0001g0012 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.378+2487_378+2488i others(34): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294111 | ||||||
| chr13:77294111
|
TATATATA others(13): Show |
T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+2468_378+2487d others(22): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294111 | ||||||
| chr13:77294113
|
T | TATACATA others(21): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.378+2485_378+2486i others(30): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294113 | ||||||
| chr13:77294113
|
T | TATACATA others(25): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013 | 3 | HG01952.hp2 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.378+2485_378+2486i others(34): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294113 | ||||||
| chr13:77294114
|
A | ATATATAC others(23): Show |
1 | a0012c0038t0002g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.378+2484_378+2485i others(32): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294114 | ||||||
| chr13:77294115
|
T | TAC | 4 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(1): Show | 4 | NA18942.hp1 NA18957.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+2483_378+2484i others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294115 | ||||||
| chr13:77294115
|
T | TACATATA others(17): Show |
1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.378+2483_378+2484i others(26): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294115 | ||||||
| chr13:77294115
|
T | TACATATA others(41): Show |
2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.378+2483_378+2484i others(50): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294115 | ||||||
| chr13:77294115
|
T | TACATATA others(17): Show |
29 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(26): Show | 29 | HG01255.hp2 HG01257.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.378+2483_378+2484i others(26): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294115 | ||||||
| chr13:77294115
|
T | TACATATA others(47): Show |
1 | a0001c0001t0001g0232 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.378+2483_378+2484i others(56): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294115 | ||||||
| chr13:77294119
|
T | TATATATA others(9): Show |
1 | a0001c0002t0001g0119 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.378+2479_378+2480i others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294119 | ||||||
| chr13:77294121
|
T | C | 2 | a0001c0005t0002g0135a0013c0037t0002g0134 | 2 | NA18977.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.378+2478A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294121 | ||||||
| chr13:77294125
|
T | TATATATA others(7): Show |
2 | a0001c0012t0001g0074a0001c0012t0001g0075 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.378+2473_378+2474i others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294125 | ||||||
| chr13:77294125
|
T | TATATATA others(11): Show |
3 | a0001c0009t0001g0077a0001c0009t0001g0220a0001c0009t0001g0310 | 3 | HG02132.hp1 HG02523.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.378+2473_378+2474i others(20): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294125 | ||||||
| chr13:77294125
|
T | TATATATA others(15): Show |
1 | a0001c0009t0001g0127 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.378+2473_378+2474i others(24): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294125 | ||||||
| chr13:77294125
|
T | TATATATA others(17): Show |
1 | a0001c0009t0001g0128 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.378+2473_378+2474i others(26): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294125 | ||||||
| chr13:77294127
|
T | C | 1 | a0001c0005t0002g0272 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.378+2472A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294127 | ||||||
| chr13:77294127
|
T | TATATATA others(25): Show |
1 | a0001c0001t0001g0176 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.378+2471_378+2472i others(34): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294127 | ||||||
| chr13:77294127
|
T | TATATATA others(9): Show |
1 | a0001c0006t0001g0318 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.378+2471_378+2472i others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294127 | ||||||
| chr13:77294127
|
T | TATATATA others(17): Show |
3 | a0001c0006t0001g0317a0001c0006t0001g0330a0001c0006t0001g0331 | 3 | HG00642.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.378+2471_378+2472i others(26): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294127 | ||||||
| chr13:77294129
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0085a0010c0025t0001g0086 | 3 | HG02145.hp2 HG02970.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.378+2470A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATACATA others(17): Show |
1 | a0001c0001t0001g0248 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.378+2469_378+2470i others(26): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATACATA others(19): Show |
1 | a0001c0026t0001g0285 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.378+2469_378+2470i others(28): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATACATA others(21): Show |
2 | a0001c0001t0001g0249a0001c0001t0001g0251 | 2 | HG00738.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.378+2469_378+2470i others(30): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATACA others(21): Show |
8 | a0001c0001t0001g0034a0001c0001t0001g0091a0001c0001t0001g0093others(5): Show | 8 | HG00423.hp2 HG00597.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.378+2469_378+2470i others(30): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATACA others(23): Show |
22 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0159others(19): Show | 22 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.378+2469_378+2470i others(32): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATACA others(25): Show |
1 | a0001c0001t0001g0282 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.378+2469_378+2470i others(34): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATACA others(27): Show |
1 | a0001c0001t0001g0167 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.378+2469_378+2470i others(36): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(23): Show |
6 | a0001c0001t0001g0089a0001c0001t0001g0095a0001c0001t0001g0175others(3): Show | 6 | HG02602.hp2 HG03704.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+2469_378+2470i others(32): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(25): Show |
10 | a0001c0001t0001g0090a0001c0001t0001g0166a0001c0001t0001g0179others(7): Show | 10 | HG01243.hp2 HG02080.hp2 HG03927.hp1 others(7): Show |
intron_variant | MODIFIER | c.378+2469_378+2470i others(34): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(27): Show |
6 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0164others(3): Show | 6 | HG01106.hp1 HG01516.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+2469_378+2470i others(36): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(29): Show |
3 | a0001c0001t0001g0043a0001c0001t0001g0161a0001c0001t0001g0165 | 3 | HG00741.hp2 HG01261.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.378+2469_378+2470i others(38): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(3): Show |
2 | a0001c0004t0001g0243a0001c0020t0001g0147 | 2 | NA18947.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.378+2469_378+2470i others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(7): Show |
4 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(1): Show | 4 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+2469_378+2470i others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(53): Show |
1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.378+2469_378+2470i others(62): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(27): Show |
1 | a0001c0001t0001g0299 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.378+2469_378+2470i others(36): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(5): Show |
12 | a0001c0001t0001g0195a0001c0001t0001g0280a0001c0001t0001g0312others(9): Show | 12 | HG00558.hp2 HG01884.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.378+2469_378+2470i others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(7): Show |
10 | a0001c0001t0001g0196a0001c0002t0001g0102a0001c0002t0001g0149others(7): Show | 10 | HG00408.hp2 HG01928.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.378+2469_378+2470i others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(33): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0283 | 2 | NA18973.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.378+2469_378+2470i others(42): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(9): Show |
5 | a0001c0004t0001g0088a0001c0004t0001g0157a0001c0004t0001g0265others(2): Show | 5 | HG00099.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+2469_378+2470i others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(11): Show |
3 | a0001c0001t0001g0197a0001c0004t0001g0278a0001c0004t0001g0293 | 3 | HG01978.hp2 HG02273.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.378+2469_378+2470i others(20): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(13): Show |
3 | a0001c0002t0001g0101a0001c0004t0001g0277a0001c0043t0001g0292 | 3 | HG00733.hp1 HG02080.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.378+2469_378+2470i others(22): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(15): Show |
1 | a0001c0004t0001g0303 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.378+2469_378+2470i others(24): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
T | TATATATA others(17): Show |
1 | a0001c0001t0001g0194 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.378+2469_378+2470i others(26): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294129
|
TAC | T | 5 | a0001c0008t0001g0296a0001c0008t0001g0305a0001c0008t0001g0306others(2): Show | 5 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+2468_378+2469d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294129 | ||||||
| chr13:77294131
|
C | CAT | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.378+2466_378+2467d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294131 | ||||||
| chr13:77294131
|
C | CATAT | 17 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(14): Show | 17 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.378+2464_378+2467d others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294131 | ||||||
| chr13:77294131
|
C | T | 124 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(121): Show | 124 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.378+2468G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294131 | ||||||
| chr13:77294337
|
T | C | 1 | a0001c0004t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.378+2262A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294337 | ||||||
| chr13:77294414
|
A | G | 1 | a0001c0043t0001g0292 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.378+2185T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294414 | ||||||
| chr13:77294511
|
G | T | 1 | a0001c0002t0001g0069 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.378+2088C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294511 | ||||||
| chr13:77294517
|
G | A | 1 | a0001c0006t0001g0320 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.378+2082C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294517 | ||||||
| chr13:77294740
|
A | T | 9 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(6): Show | 9 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.378+1859T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294740 | ||||||
| chr13:77294791
|
C | G | 1 | a0001c0001t0001g0250 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.378+1808G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294791 | ||||||
| chr13:77294813
|
G | A | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.378+1786C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294813 | ||||||
| chr13:77294838
|
T | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+1761A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77294838 | ||||||
| chr13:77295043
|
G | A | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+1556C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77295043 | ||||||
| chr13:77295107
|
G | T | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.378+1492C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77295107 | ||||||
| chr13:77295238
|
A | G | 1 | a0004c0011t0001g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.378+1361T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77295238 | ||||||
| chr13:77295283
|
A | G | 132 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(129): Show | 132 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.378+1316T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77295283 | ||||||
| chr13:77295354
|
G | A | 1 | a0001c0023t0001g0206 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.378+1245C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77295354 | ||||||
| chr13:77295360
|
T | C | 1 | a0001c0020t0001g0147 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.378+1239A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77295360 | ||||||
| chr13:77295376
|
C | T | 1 | a0001c0009t0001g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.378+1223G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77295376 | ||||||
| chr13:77295399
|
G | A | 3 | a0001c0001t0001g0280a0001c0004t0001g0088a0001c0004t0001g0151 | 3 | HG02258.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.378+1200C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77295399 | ||||||
| chr13:77295411
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.378+1188G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77295411 | ||||||
| chr13:77295542
|
T | A | 1 | a0001c0021t0001g0301 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.378+1057A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77295542 | ||||||
| chr13:77295557
|
T | C | 1 | a0001c0002t0002g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.378+1042A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77295557 | ||||||
| chr13:77296153
|
C | T | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+446G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 2/82 | chr13 | 77296153 | ||||||
| chr13:77296695
|
G | A | 4 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.303-21C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77296695 | ||||||
| chr13:77296824
|
T | C | 1 | a0014c0032t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.303-150A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77296824 | ||||||
| chr13:77296844
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.303-170A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77296844 | ||||||
| chr13:77296977
|
T | A | 2 | a0001c0002t0001g0048a0001c0002t0001g0067 | 2 | NA18979.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.303-303A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77296977 | ||||||
| chr13:77297236
|
T | G | 1 | a0001c0021t0001g0301 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.303-562A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77297236 | ||||||
| chr13:77297305
|
T | C | 4 | a0001c0006t0001g0323a0001c0006t0001g0324a0001c0006t0001g0325others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-631A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77297305 | ||||||
| chr13:77297314
|
T | C | 1 | a0001c0005t0002g0273 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.303-640A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77297314 | ||||||
| chr13:77297470
|
A | G | 9 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(6): Show | 9 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.303-796T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77297470 | ||||||
| chr13:77297509
|
C | G | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-835G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77297509 | ||||||
| chr13:77297590
|
A | G | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.303-916T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77297590 | ||||||
| chr13:77297762
|
T | C | 1 | a0001c0002t0001g0203 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.303-1088A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77297762 | ||||||
| chr13:77297806
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.303-1132C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77297806 | ||||||
| chr13:77297831
|
A | C | 113 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(110): Show | 113 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.303-1157T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77297831 | ||||||
| chr13:77297881
|
TACC | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-1210_303-1208d others(5): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77297881 | ||||||
| chr13:77297981
|
A | G | 1 | a0001c0002t0001g0115 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.303-1307T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77297981 | ||||||
| chr13:77298064
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.303-1390C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77298064 | ||||||
| chr13:77298069
|
C | T | 1 | a0001c0004t0001g0265 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.303-1395G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77298069 | ||||||
| chr13:77298269
|
A | G | 1 | a0001c0003t0001g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.303-1595T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77298269 | ||||||
| chr13:77298995
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.303-2321G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77298995 | ||||||
| chr13:77298996
|
G | A | 2 | a0001c0002t0001g0001a0001c0002t0001g0114 | 3 | HG03490.hp1 HG03492.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.303-2322C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77298996 | ||||||
| chr13:77299010
|
A | AT | 114 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(111): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.303-2337dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299010 | ||||||
| chr13:77299075
|
G | A | 7 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.303-2401C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299075 | ||||||
| chr13:77299139
|
C | G | 113 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(110): Show | 113 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.303-2465G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299139 | ||||||
| chr13:77299207
|
T | C | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.303-2533A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299207 | ||||||
| chr13:77299320
|
G | T | 7 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(4): Show | 7 | HG00621.hp1 HG02132.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.303-2646C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299320 | ||||||
| chr13:77299398
|
C | G | 111 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(108): Show | 111 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.303-2724G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299398 | ||||||
| chr13:77299444
|
G | T | 1 | a0002c0007t0001g0217 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.303-2770C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299444 | ||||||
| chr13:77299461
|
G | A | 3 | a0001c0005t0002g0221a0001c0005t0002g0272a0001c0005t0002g0273 | 3 | HG01928.hp1 HG02132.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.303-2787C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299461 | ||||||
| chr13:77299577
|
T | C | 8 | a0001c0004t0001g0087a0001c0004t0001g0153a0001c0004t0001g0240others(5): Show | 8 | HG00621.hp2 NA18946.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.303-2903A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299577 | ||||||
| chr13:77299657
|
A | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-2983T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299657 | ||||||
| chr13:77299736
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.303-3062C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299736 | ||||||
| chr13:77299755
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.303-3081G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299755 | ||||||
| chr13:77299819
|
A | G | 20 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(17): Show | 20 | HG00099.hp1 HG01928.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.303-3145T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299819 | ||||||
| chr13:77299865
|
T | A | 1 | a0001c0034t0001g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.303-3191A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77299865 | ||||||
| chr13:77300162
|
C | T | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.303-3488G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77300162 | ||||||
| chr13:77300253
|
T | G | 4 | a0001c0004t0001g0155a0004c0011t0001g0148a0004c0011t0001g0152others(1): Show | 4 | HG00558.hp2 NA18950.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-3579A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77300253 | ||||||
| chr13:77300393
|
G | A | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-3719C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77300393 | ||||||
| chr13:77300460
|
T | A | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-3786A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77300460 | ||||||
| chr13:77300532
|
G | T | 4 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.303-3858C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77300532 | ||||||
| chr13:77300917
|
C | T | 205 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.303-4243G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77300917 | ||||||
| chr13:77300993
|
T | C | 113 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(110): Show | 113 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.303-4319A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77300993 | ||||||
| chr13:77301081
|
C | G | 1 | a0002c0040t0001g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.303-4407G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301081 | ||||||
| chr13:77301181
|
G | A | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-4507C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301181 | ||||||
| chr13:77301252
|
T | C | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-4578A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301252 | ||||||
| chr13:77301377
|
C | T | 74 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(71): Show | 74 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.303-4703G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301377 | ||||||
| chr13:77301379
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0300 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.303-4705G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301379 | ||||||
| chr13:77301388
|
A | G | 2 | a0001c0004t0001g0153a0001c0004t0001g0240 | 2 | NA18946.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.303-4714T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301388 | ||||||
| chr13:77301402
|
T | A | 1 | a0001c0002t0001g0123 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.303-4728A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301402 | ||||||
| chr13:77301409
|
C | G | 9 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(6): Show | 9 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.303-4735G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301409 | ||||||
| chr13:77301415
|
TC | T | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.303-4742delG | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301415 | ||||||
| chr13:77301422
|
C | CA | 16 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(13): Show | 16 | HG00735.hp2 HG01952.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.303-4749dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301422 | ||||||
| chr13:77301422
|
CA | C | 132 | a0001c0001t0001g0007a0001c0001t0001g0080a0001c0001t0001g0081others(129): Show | 133 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.303-4749delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301422 | ||||||
| chr13:77301422
|
CAA | C | 14 | a0001c0001t0001g0141a0001c0002t0001g0049a0001c0002t0001g0058others(11): Show | 14 | HG00408.hp1 HG00558.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.303-4750_303-4749d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301422 | ||||||
| chr13:77301422
|
CAAAAAAA others(4): Show |
C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.303-4759_303-4749d others(13): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301422 | ||||||
| chr13:77301422
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.303-4761_303-4749d others(15): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301422 | ||||||
| chr13:77301422
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0006t0001g0328a0001c0006t0001g0329 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.303-4762_303-4749d others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301422 | ||||||
| chr13:77301422
|
CAAAAAAA others(9): Show |
C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.303-4764_303-4749d others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301422 | ||||||
| chr13:77301448
|
A | AC | 12 | a0001c0001t0001g0094a0001c0001t0001g0130a0001c0001t0001g0159others(9): Show | 12 | HG00438.hp1 HG01071.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.303-4775_303-4774i others(3): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301448 | ||||||
| chr13:77301448
|
A | C | 100 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(97): Show | 100 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.303-4774T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301448 | ||||||
| chr13:77301542
|
A | T | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.303-4868T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301542 | ||||||
| chr13:77301708
|
T | C | 2 | a0001c0003t0001g0015a0001c0003t0001g0017 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.303-5034A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301708 | ||||||
| chr13:77301765
|
G | T | 1 | a0001c0003t0001g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.303-5091C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301765 | ||||||
| chr13:77301816
|
G | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.303-5142C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301816 | ||||||
| chr13:77301920
|
T | C | 1 | a0001c0002t0001g0110 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.303-5246A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77301920 | ||||||
| chr13:77302103
|
G | C | 11 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG02027.hp2 HG02071.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.303-5429C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77302103 | ||||||
| chr13:77302270
|
A | G | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.303-5596T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77302270 | ||||||
| chr13:77302491
|
G | C | 114 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(111): Show | 114 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.303-5817C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77302491 | ||||||
| chr13:77302513
|
C | G | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-5839G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77302513 | ||||||
| chr13:77303061
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(70): Show | 73 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.303-6387C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303061 | ||||||
| chr13:77303075
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.303-6401G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303075 | ||||||
| chr13:77303087
|
C | A | 1 | a0001c0001t0001g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.303-6413G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303087 | ||||||
| chr13:77303282
|
T | G | 113 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(110): Show | 113 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.303-6608A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303282 | ||||||
| chr13:77303316
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.303-6642C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303316 | ||||||
| chr13:77303368
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0013 | 2 | HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.303-6694G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303368 | ||||||
| chr13:77303390
|
A | G | 113 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(110): Show | 113 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.303-6716T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303390 | ||||||
| chr13:77303700
|
C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.303-7026G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303700 | ||||||
| chr13:77303717
|
C | T | 2 | a0001c0003t0001g0041a0001c0003t0001g0042 | 2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.303-7043G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303717 | ||||||
| chr13:77303718
|
G | A | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | NA18947.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.303-7044C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303718 | ||||||
| chr13:77303743
|
C | G | 1 | a0001c0006t0001g0322 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303-7069G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303743 | ||||||
| chr13:77303755
|
C | T | 1 | a0001c0008t0001g0306 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.303-7081G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303755 | ||||||
| chr13:77303771
|
G | GA | 122 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(119): Show | 122 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.303-7098dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77303771 | ||||||
| chr13:77304061
|
T | C | 5 | a0001c0005t0002g0222a0001c0005t0002g0224a0001c0005t0002g0268others(2): Show | 5 | NA18952.hp1 NA18982.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-7387A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77304061 | ||||||
| chr13:77304165
|
A | C | 2 | a0003c0010t0001g0111a0003c0010t0001g0112 | 2 | NA18943.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.303-7491T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77304165 | ||||||
| chr13:77304545
|
G | T | 1 | a0001c0001t0001g0239 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.303-7871C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77304545 | ||||||
| chr13:77304564
|
A | G | 1 | a0001c0031t0001g0070 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.303-7890T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77304564 | ||||||
| chr13:77304867
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.303-8193G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77304867 | ||||||
| chr13:77304952
|
GA | G | 11 | a0001c0001t0001g0013a0001c0003t0001g0129a0001c0009t0001g0076others(8): Show | 11 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.303-8279delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77304952 | ||||||
| chr13:77304986
|
T | C | 1 | a0001c0021t0001g0301 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.303-8312A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77304986 | ||||||
| chr13:77305134
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-8460A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77305134 | ||||||
| chr13:77305241
|
G | A | 83 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(80): Show | 84 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.303-8567C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77305241 | ||||||
| chr13:77305667
|
C | G | 1 | a0001c0001t0001g0316 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.303-8993G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77305667 | ||||||
| chr13:77305683
|
AAGAG | A | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.303-9013_303-9010d others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77305683 | ||||||
| chr13:77306287
|
A | G | 1 | a0001c0003t0001g0016 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.303-9613T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77306287 | ||||||
| chr13:77306315
|
G | A | 2 | a0001c0003t0001g0260a0001c0003t0001g0261 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.303-9641C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77306315 | ||||||
| chr13:77306426
|
G | A | 10 | a0001c0006t0001g0317a0001c0006t0001g0318a0001c0006t0001g0321others(7): Show | 10 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.303-9752C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77306426 | ||||||
| chr13:77306490
|
G | T | 6 | a0001c0004t0001g0265a0001c0004t0001g0266a0001c0004t0001g0267others(3): Show | 6 | HG01071.hp2 HG01261.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-9816C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77306490 | ||||||
| chr13:77306502
|
T | C | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0304 | 3 | HG00673.hp2 NA18945.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.303-9828A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77306502 | ||||||
| chr13:77306594
|
T | A | 6 | a0001c0004t0001g0087a0001c0004t0001g0153a0001c0004t0001g0240others(3): Show | 6 | HG00621.hp2 NA18946.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.303-9920A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77306594 | ||||||
| chr13:77306640
|
C | A | 1 | a0001c0004t0001g0277 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.303-9966G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77306640 | ||||||
| chr13:77306717
|
T | C | 1 | a0016c0028t0001g0241 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.303-10043A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77306717 | ||||||
| chr13:77306795
|
C | T | 1 | a0006c0017t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.303-10121G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77306795 | ||||||
| chr13:77307075
|
T | C | 9 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(6): Show | 9 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.303-10401A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307075 | ||||||
| chr13:77307095
|
G | A | 49 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(46): Show | 49 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.303-10421C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307095 | ||||||
| chr13:77307378
|
T | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-10704A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307378 | ||||||
| chr13:77307507
|
T | TCCCAGCT others(7): Show |
1 | a0001c0005t0002g0271 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.303-10847_303-1083 others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307507 | ||||||
| chr13:77307625
|
C | CA | 114 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0043others(111): Show | 115 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.303-10952dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307625 | ||||||
| chr13:77307625
|
C | CAA | 43 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0144others(40): Show | 43 | HG00423.hp1 HG00609.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.303-10953_303-1095 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307625 | ||||||
| chr13:77307625
|
C | CAAA | 11 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(8): Show | 11 | HG00544.hp2 HG01934.hp1 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.303-10954_303-1095 others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307625 | ||||||
| chr13:77307625
|
C | CAAAA | 10 | a0001c0001t0001g0085a0001c0001t0001g0139a0001c0001t0001g0226others(7): Show | 10 | HG00438.hp2 HG01255.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.303-10955_303-1095 others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307625 | ||||||
| chr13:77307625
|
CAAAAAAA others(2): Show |
C | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.303-10960_303-1095 others(13): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307625 | ||||||
| chr13:77307625
|
CAAAAAAA others(3): Show |
C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.303-10961_303-1095 others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307625 | ||||||
| chr13:77307639
|
A | C | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.303-10965T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307639 | ||||||
| chr13:77307640
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.303-10966T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307640 | ||||||
| chr13:77307643
|
A | C | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.303-10969T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307643 | ||||||
| chr13:77307644
|
A | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.303-10970T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307644 | ||||||
| chr13:77307972
|
G | A | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.303-11298C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77307972 | ||||||
| chr13:77308504
|
T | C | 9 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(6): Show | 9 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.303-11830A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77308504 | ||||||
| chr13:77308687
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.303-12013C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77308687 | ||||||
| chr13:77308889
|
C | T | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-12215G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77308889 | ||||||
| chr13:77309082
|
A | C | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.303-12408T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77309082 | ||||||
| chr13:77309321
|
T | C | 1 | a0001c0002t0001g0119 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.303-12647A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77309321 | ||||||
| chr13:77309366
|
T | C | 1 | a0001c0002t0001g0257 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.303-12692A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77309366 | ||||||
| chr13:77309578
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.303-12904A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77309578 | ||||||
| chr13:77309704
|
G | A | 1 | a0001c0003t0001g0033 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.303-13030C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77309704 | ||||||
| chr13:77309711
|
T | C | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.303-13037A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77309711 | ||||||
| chr13:77309847
|
C | G | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-13173G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77309847 | ||||||
| chr13:77309853
|
C | A | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-13179G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77309853 | ||||||
| chr13:77309876
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.303-13202C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77309876 | ||||||
| chr13:77309995
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.303-13321G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77309995 | ||||||
| chr13:77310105
|
C | T | 1 | a0001c0003t0006g0209 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.303-13431G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77310105 | ||||||
| chr13:77310255
|
C | T | 1 | a0001c0002t0001g0199 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.303-13581G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77310255 | ||||||
| chr13:77310329
|
T | C | 1 | a0001c0002t0001g0201 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.303-13655A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77310329 | ||||||
| chr13:77310567
|
T | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.303-13893A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77310567 | ||||||
| chr13:77310645
|
T | C | 14 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(11): Show | 14 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.303-13971A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77310645 | ||||||
| chr13:77310777
|
C | T | 1 | a0001c0006t0001g0321 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.303-14103G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77310777 | ||||||
| chr13:77310786
|
G | GCA | 121 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(118): Show | 121 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.303-14114_303-1411 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77310786 | ||||||
| chr13:77310863
|
T | A | 330 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.303-14189A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77310863 | ||||||
| chr13:77311495
|
T | C | 3 | a0001c0005t0002g0138a0001c0005t0002g0223a0001c0005t0002g0271 | 3 | HG00099.hp1 NA18995.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.303-14821A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77311495 | ||||||
| chr13:77311506
|
C | T | 9 | a0001c0009t0001g0076a0001c0009t0001g0077a0001c0009t0001g0127others(6): Show | 9 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.303-14832G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77311506 | ||||||
| chr13:77311555
|
GTTTTTTT others(7): Show |
G | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG01257.hp1 HG01891.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.303-14895_303-1488 others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77311555 | ||||||
| chr13:77311565
|
G | GT | 8 | a0001c0001t0001g0130a0001c0001t0001g0163a0001c0003t0001g0096others(5): Show | 8 | HG00438.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.303-14892dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77311565 | ||||||
| chr13:77311565
|
G | GTT | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.303-14893_303-1489 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77311565 | ||||||
| chr13:77311565
|
GT | G | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.303-14892delA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77311565 | ||||||
| chr13:77311570
|
T | G | 1 | a0001c0005t0002g0138 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.303-14896A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77311570 | ||||||
| chr13:77311579
|
G | GT | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.302+14894dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77311579 | ||||||
| chr13:77311581
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.302+14893A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77311581 | ||||||
| chr13:77311671
|
T | C | 8 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(5): Show | 8 | HG02071.hp2 NA18960.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+14803A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77311671 | ||||||
| chr13:77311698
|
C | T | 1 | a0001c0019t0001g0274 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.302+14776G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77311698 | ||||||
| chr13:77312010
|
C | A | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.302+14464G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77312010 | ||||||
| chr13:77312154
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.302+14320A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77312154 | ||||||
| chr13:77312260
|
G | A | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | NA18947.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.302+14214C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77312260 | ||||||
| chr13:77312333
|
A | T | 1 | a0001c0004t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.302+14141T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77312333 | ||||||
| chr13:77312598
|
T | C | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.302+13876A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77312598 | ||||||
| chr13:77312825
|
C | CT | 9 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(6): Show | 9 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.302+13648dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77312825 | ||||||
| chr13:77313085
|
T | A | 1 | a0001c0014t0001g0050 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.302+13389A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77313085 | ||||||
| chr13:77313291
|
T | C | 108 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(105): Show | 108 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.302+13183A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77313291 | ||||||
| chr13:77313495
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.302+12979G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77313495 | ||||||
| chr13:77313789
|
A | C | 1 | a0001c0009t0001g0076 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.302+12685T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77313789 | ||||||
| chr13:77313880
|
T | C | 6 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(3): Show | 6 | HG00741.hp1 HG01496.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+12594A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77313880 | ||||||
| chr13:77313896
|
G | T | 9 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(6): Show | 9 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.302+12578C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77313896 | ||||||
| chr13:77313925
|
C | T | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.302+12549G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77313925 | ||||||
| chr13:77313994
|
T | C | 1 | a0001c0002t0001g0120 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.302+12480A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77313994 | ||||||
| chr13:77314033
|
G | T | 1 | a0001c0002t0001g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.302+12441C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77314033 | ||||||
| chr13:77314151
|
C | T | 49 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(46): Show | 49 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.302+12323G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77314151 | ||||||
| chr13:77314361
|
A | T | 2 | a0001c0005t0002g0223a0001c0005t0002g0271 | 2 | NA18995.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.302+12113T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77314361 | ||||||
| chr13:77314384
|
T | C | 1 | a0001c0002t0001g0203 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.302+12090A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77314384 | ||||||
| chr13:77314583
|
T | TA | 35 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(32): Show | 35 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.302+11890dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77314583 | ||||||
| chr13:77314732
|
G | C | 1 | a0001c0002t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.302+11742C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77314732 | ||||||
| chr13:77314745
|
T | A | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.302+11729A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77314745 | ||||||
| chr13:77314756
|
G | A | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.302+11718C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77314756 | ||||||
| chr13:77314975
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.302+11499A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77314975 | ||||||
| chr13:77315017
|
T | C | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.302+11457A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315017 | ||||||
| chr13:77315081
|
C | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.302+11393G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315081 | ||||||
| chr13:77315082
|
C | A | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.302+11392G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315082 | ||||||
| chr13:77315120
|
G | A | 29 | a0001c0001t0001g0280a0001c0002t0001g0149a0001c0004t0001g0087others(26): Show | 29 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.302+11354C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315120 | ||||||
| chr13:77315439
|
T | C | 9 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(6): Show | 9 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.302+11035A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315439 | ||||||
| chr13:77315617
|
G | A | 3 | a0001c0006t0001g0319a0001c0006t0001g0320a0001c0006t0001g0322 | 3 | HG01891.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.302+10857C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315617 | ||||||
| chr13:77315663
|
G | A | 1 | a0002c0007t0001g0219 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.302+10811C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315663 | ||||||
| chr13:77315820
|
G | A | 2 | a0001c0002t0001g0048a0001c0002t0001g0067 | 2 | NA18979.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.302+10654C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315820 | ||||||
| chr13:77315894
|
C | CA | 7 | a0001c0002t0001g0101a0001c0002t0001g0105a0001c0002t0001g0204others(4): Show | 7 | HG01109.hp1 HG02886.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.302+10579dupT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315894 | ||||||
| chr13:77315894
|
CA | C | 109 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(106): Show | 109 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.302+10579delT | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315894 | ||||||
| chr13:77315894
|
CAA | C | 40 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(37): Show | 40 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.302+10578_302+1057 others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315894 | ||||||
| chr13:77315984
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.302+10490G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77315984 | ||||||
| chr13:77316132
|
C | T | 9 | a0001c0001t0001g0034a0001c0001t0001g0163a0001c0001t0001g0173others(6): Show | 9 | HG00280.hp2 HG00738.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.302+10342G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77316132 | ||||||
| chr13:77316280
|
G | A | 1 | a0004c0011t0001g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.302+10194C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77316280 | ||||||
| chr13:77316409
|
T | C | 1 | a0001c0004t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.302+10065A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77316409 | ||||||
| chr13:77316534
|
C | T | 1 | a0001c0033t0001g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.302+9940G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77316534 | ||||||
| chr13:77316684
|
G | A | 1 | a0001c0005t0002g0138 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.302+9790C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77316684 | ||||||
| chr13:77316703
|
T | TACTAGCC others(52): Show |
4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(1): Show | 4 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+9712_302+9770d others(61): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77316703 | ||||||
| chr13:77316729
|
C | G | 21 | a0001c0005t0002g0078a0001c0005t0002g0079a0001c0005t0002g0131others(18): Show | 21 | HG00099.hp1 HG01496.hp2 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.302+9745G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77316729 | ||||||
| chr13:77316825
|
G | A | 1 | a0001c0003t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.302+9649C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77316825 | ||||||
| chr13:77316867
|
C | T | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+9607G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77316867 | ||||||
| chr13:77316952
|
G | GT | 97 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(94): Show | 97 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.302+9521dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77316952 | ||||||
| chr13:77317096
|
C | T | 89 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.302+9378G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317096 | ||||||
| chr13:77317209
|
C | T | 1 | a0001c0002t0001g0125 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.302+9265G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317209 | ||||||
| chr13:77317219
|
T | C | 1 | a0001c0002t0001g0201 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.302+9255A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317219 | ||||||
| chr13:77317242
|
G | A | 1 | a0001c0002t0001g0205 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.302+9232C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317242 | ||||||
| chr13:77317516
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.302+8958C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317516 | ||||||
| chr13:77317661
|
G | A | 1 | a0001c0003t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.302+8813C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317661 | ||||||
| chr13:77317662
|
G | T | 1 | a0001c0001t0001g0007 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.302+8812C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317662 | ||||||
| chr13:77317714
|
G | A | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.302+8760C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317714 | ||||||
| chr13:77317735
|
G | A | 8 | a0001c0003t0001g0028a0001c0003t0001g0029a0001c0003t0001g0031others(5): Show | 8 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.302+8739C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317735 | ||||||
| chr13:77317758
|
G | A | 31 | a0001c0003t0001g0129a0001c0005t0002g0078a0001c0005t0002g0079others(28): Show | 31 | HG00099.hp1 HG00621.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.302+8716C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317758 | ||||||
| chr13:77317798
|
G | A | 6 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+8676C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317798 | ||||||
| chr13:77317894
|
G | A | 1 | a0001c0006t0001g0333 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.302+8580C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317894 | ||||||
| chr13:77317938
|
A | AAACAT | 44 | a0001c0001t0001g0008a0001c0001t0001g0089a0001c0001t0001g0140others(41): Show | 44 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.302+8531_302+8535d others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317938 | ||||||
| chr13:77317938
|
A | AAACATAA others(3): Show |
11 | a0001c0001t0001g0080a0001c0001t0001g0139a0001c0001t0001g0227others(8): Show | 11 | HG00597.hp2 HG00642.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.302+8526_302+8535d others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317938 | ||||||
| chr13:77317938
|
A | AAACATAA others(8): Show |
2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG01981.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.302+8521_302+8535d others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317938 | ||||||
| chr13:77317938
|
A | AAACATAA others(13): Show |
3 | a0001c0002t0001g0048a0001c0012t0001g0074a0001c0012t0001g0075 | 3 | HG01069.hp2 HG01071.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.302+8516_302+8535d others(22): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317938 | ||||||
| chr13:77317938
|
AAACAT | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.302+8531_302+8535d others(7): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317938 | ||||||
| chr13:77317938
|
AAACATAA others(3): Show |
A | 50 | a0001c0001t0001g0043a0001c0001t0001g0094a0001c0001t0001g0146others(47): Show | 50 | HG00099.hp1 HG00673.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.302+8526_302+8535d others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317938 | ||||||
| chr13:77317938
|
AAACATAA others(8): Show |
A | 7 | a0001c0001t0001g0211a0001c0002t0001g0124a0001c0003t0001g0289others(4): Show | 7 | HG01261.hp2 HG02004.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.302+8521_302+8535d others(17): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317938 | ||||||
| chr13:77317938
|
AAACATAA others(13): Show |
A | 9 | a0001c0003t0001g0260a0001c0003t0001g0261a0002c0007t0001g0212others(6): Show | 9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.302+8516_302+8535d others(22): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317938 | ||||||
| chr13:77317938
|
AAACATAA others(18): Show |
A | 1 | a0002c0040t0001g0297 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.302+8511_302+8535d others(27): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77317938 | ||||||
| chr13:77318014
|
C | T | 41 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(38): Show | 41 | HG00438.hp2 HG01255.hp2 HG01257.hp1 others(38): Show |
intron_variant | MODIFIER | c.302+8460G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77318014 | ||||||
| chr13:77318470
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.302+8004T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77318470 | ||||||
| chr13:77318626
|
C | T | 1 | a0001c0009t0001g0220 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.302+7848G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77318626 | ||||||
| chr13:77318733
|
G | T | 1 | a0002c0007t0001g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.302+7741C>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77318733 | ||||||
| chr13:77318741
|
G | A | 1 | a0001c0003t0001g0033 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.302+7733C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77318741 | ||||||
| chr13:77318754
|
AAAAC | A | 4 | a0001c0006t0001g0323a0001c0006t0001g0324a0001c0006t0001g0325others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+7716_302+7719d others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77318754 | ||||||
| chr13:77318801
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.302+7673C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77318801 | ||||||
| chr13:77318853
|
T | C | 204 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.302+7621A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77318853 | ||||||
| chr13:77318944
|
A | C | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+7530T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77318944 | ||||||
| chr13:77318983
|
G | A | 2 | a0001c0001t0001g0085a0010c0025t0001g0086 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.302+7491C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77318983 | ||||||
| chr13:77319125
|
T | A | 1 | a0001c0004t0001g0287 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.302+7349A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77319125 | ||||||
| chr13:77319154
|
C | G | 1 | a0001c0001t0001g0281 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.302+7320G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77319154 | ||||||
| chr13:77319225
|
C | G | 49 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(46): Show | 49 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.302+7249G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77319225 | ||||||
| chr13:77319226
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0255 | 2 | NA18943.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.302+7248C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77319226 | ||||||
| chr13:77319287
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.302+7187A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77319287 | ||||||
| chr13:77319300
|
C | T | 2 | a0001c0002t0001g0099a0001c0002t0001g0100 | 2 | NA18947.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.302+7174G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77319300 | ||||||
| chr13:77319476
|
T | C | 140 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(137): Show | 140 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.302+6998A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77319476 | ||||||
| chr13:77319569
|
C | A | 9 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(6): Show | 9 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.302+6905G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77319569 | ||||||
| chr13:77319835
|
A | C | 1 | a0001c0001t0001g0007 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.302+6639T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77319835 | ||||||
| chr13:77319952
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.302+6522C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77319952 | ||||||
| chr13:77320116
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.302+6358G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320116 | ||||||
| chr13:77320151
|
TAGATGTA others(3): Show |
T | 1 | a0001c0001t0001g0007 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.302+6313_302+6322d others(12): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320151 | ||||||
| chr13:77320290
|
A | T | 1 | a0001c0030t0001g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.302+6184T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320290 | ||||||
| chr13:77320569
|
G | GT | 3 | a0001c0004t0001g0265a0001c0004t0001g0266a0001c0004t0001g0267 | 3 | HG01071.hp2 HG01261.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.302+5904dupA | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320569 | ||||||
| chr13:77320575
|
G | A | 5 | a0001c0003t0001g0047a0001c0003t0001g0097a0001c0003t0001g0098others(2): Show | 5 | HG00741.hp1 HG01496.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+5899C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320575 | ||||||
| chr13:77320671
|
G | A | 73 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0043others(70): Show | 73 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.302+5803C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320671 | ||||||
| chr13:77320734
|
G | C | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.302+5740C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320734 | ||||||
| chr13:77320756
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.302+5718G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320756 | ||||||
| chr13:77320769
|
A | C | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+5705T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320769 | ||||||
| chr13:77320784
|
T | A | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.302+5690A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320784 | ||||||
| chr13:77320808
|
C | T | 1 | a0001c0002t0001g0036 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.302+5666G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320808 | ||||||
| chr13:77320966
|
G | A | 1 | a0001c0002t0001g0125 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.302+5508C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77320966 | ||||||
| chr13:77321004
|
T | C | 2 | a0001c0003t0001g0295a0001c0021t0001g0301 | 2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.302+5470A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77321004 | ||||||
| chr13:77321007
|
A | G | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.302+5467T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77321007 | ||||||
| chr13:77321433
|
A | G | 1 | a0006c0017t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.302+5041T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77321433 | ||||||
| chr13:77321510
|
T | C | 5 | a0001c0003t0001g0014a0001c0003t0001g0044a0001c0003t0001g0046others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+4964A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77321510 | ||||||
| chr13:77321661
|
T | A | 1 | a0001c0001t0001g0007 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.302+4813A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77321661 | ||||||
| chr13:77321706
|
C | T | 1 | a0001c0009t0001g0311 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.302+4768G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77321706 | ||||||
| chr13:77321777
|
G | A | 18 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(15): Show | 18 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.302+4697C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77321777 | ||||||
| chr13:77321825
|
T | C | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.302+4649A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77321825 | ||||||
| chr13:77321858
|
C | T | 1 | a0001c0009t0001g0310 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.302+4616G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77321858 | ||||||
| chr13:77321929
|
G | A | 1 | a0001c0003t0001g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.302+4545C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77321929 | ||||||
| chr13:77322137
|
C | A | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.302+4337G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77322137 | ||||||
| chr13:77322300
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.302+4174G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77322300 | ||||||
| chr13:77322328
|
T | C | 1 | a0001c0004t0001g0287 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.302+4146A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77322328 | ||||||
| chr13:77322814
|
T | G | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.302+3660A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77322814 | ||||||
| chr13:77322869
|
G | A | 10 | a0001c0001t0001g0193a0001c0001t0001g0256a0001c0001t0001g0262others(7): Show | 10 | HG00544.hp1 HG00741.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.302+3605C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77322869 | ||||||
| chr13:77322955
|
C | T | 213 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.302+3519G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77322955 | ||||||
| chr13:77323356
|
T | C | 1 | a0012c0038t0002g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.302+3118A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77323356 | ||||||
| chr13:77323452
|
C | T | 14 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(11): Show | 14 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.302+3022G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77323452 | ||||||
| chr13:77323576
|
T | C | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.302+2898A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77323576 | ||||||
| chr13:77323710
|
G | A | 6 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0289others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+2764C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77323710 | ||||||
| chr13:77323814
|
C | A | 92 | a0001c0002t0001g0001a0001c0002t0001g0025a0001c0002t0001g0026others(89): Show | 93 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.302+2660G>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77323814 | ||||||
| chr13:77323846
|
A | G | 10 | a0001c0003t0001g0129a0001c0009t0001g0076a0001c0009t0001g0077others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.302+2628T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77323846 | ||||||
| chr13:77323848
|
C | T | 1 | a0001c0036t0001g0291 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.302+2626G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77323848 | ||||||
| chr13:77323977
|
CCT | C | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.302+2495_302+2496d others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77323977 | ||||||
| chr13:77323991
|
T | A | 2 | a0001c0001t0001g0262a0001c0001t0001g0290 | 2 | HG00544.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.302+2483A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77323991 | ||||||
| chr13:77324014
|
T | G | 1 | a0001c0023t0001g0206 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.302+2460A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77324014 | ||||||
| chr13:77324017
|
C | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.302+2457G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77324017 | ||||||
| chr13:77324085
|
G | C | 1 | a0001c0045t0001g0327 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.302+2389C>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77324085 | ||||||
| chr13:77324561
|
C | T | 330 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(327): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.302+1913G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77324561 | ||||||
| chr13:77324773
|
A | G | 1 | a0006c0017t0001g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.302+1701T>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77324773 | ||||||
| chr13:77324780
|
T | C | 1 | a0001c0003t0001g0210 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.302+1694A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77324780 | ||||||
| chr13:77324968
|
T | G | 4 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0005others(1): Show | 4 | NA18942.hp1 NA18957.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.302+1506A>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77324968 | ||||||
| chr13:77325177
|
C | T | 13 | a0001c0003t0001g0027a0001c0003t0001g0041a0001c0003t0001g0042others(10): Show | 13 | HG00735.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.302+1297G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77325177 | ||||||
| chr13:77325770
|
C | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.302+704G>C | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77325770 | ||||||
| chr13:77325811
|
A | T | 2 | a0001c0003t0001g0071a0001c0003t0001g0072 | 2 | HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.302+663T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77325811 | ||||||
| chr13:77326005
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.302+469C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326005 | ||||||
| chr13:77326040
|
A | C | 1 | a0001c0001t0001g0007 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.302+434T>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326040 | ||||||
| chr13:77326041
|
T | A | 1 | a0001c0001t0001g0007 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.302+433A>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326041 | ||||||
| chr13:77326041
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.302+433A>G | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326041 | ||||||
| chr13:77326072
|
C | T | 8 | a0001c0008t0001g0263a0001c0008t0001g0296a0001c0008t0001g0302others(5): Show | 8 | HG00735.hp2 HG02109.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.302+402G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326072 | ||||||
| chr13:77326228
|
C | T | 1 | a0001c0031t0001g0070 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.302+246G>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326228 | ||||||
| chr13:77326240
|
G | GAC | 55 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(52): Show | 55 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.302+232_302+233dup others(2): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
G | GACAC | 29 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0280others(26): Show | 29 | HG00544.hp1 HG00733.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.302+230_302+233dup others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
G | GACACAC | 5 | a0001c0001t0001g0294a0001c0003t0001g0295a0001c0004t0001g0293others(2): Show | 5 | HG00280.hp2 HG02055.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+228_302+233dup others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
G | GACACACA others(1): Show |
6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG00673.hp2 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+226_302+233dup others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
G | GACACACA others(3): Show |
3 | a0001c0001t0001g0304a0001c0004t0001g0303a0001c0008t0001g0302 | 3 | HG01952.hp1 HG03139.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.302+224_302+233dup others(10): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
G | GACACACA others(7): Show |
4 | a0001c0008t0001g0305a0001c0008t0001g0306a0001c0008t0001g0307others(1): Show | 4 | HG00735.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.302+220_302+233dup others(14): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
G | GACACACA others(9): Show |
1 | a0001c0008t0001g0309 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.302+218_302+233dup others(16): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
GAC | G | 65 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(62): Show | 65 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.302+232_302+233del others(2): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
GACAC | G | 40 | a0001c0001t0001g0043a0001c0002t0001g0048a0001c0002t0001g0049others(37): Show | 40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.302+230_302+233del others(4): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
GACACAC | G | 15 | a0001c0001t0001g0034a0001c0002t0001g0036a0001c0002t0001g0039others(12): Show | 15 | HG00280.hp1 HG01099.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.302+228_302+233del others(6): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
GACACACA others(1): Show |
G | 3 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0034t0001g0024 | 3 | HG00544.hp2 HG02622.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.302+226_302+233del others(8): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
GACACACA others(11): Show |
G | 9 | a0001c0003t0001g0015a0001c0003t0001g0016a0001c0003t0001g0017others(6): Show | 9 | HG02717.hp2 HG02809.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.302+216_302+233del others(18): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326240
|
GACACACA others(19): Show |
G | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG01891.hp1 HG01952.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.302+208_302+233del others(26): Show |
MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326240 | ||||||
| chr13:77326365
|
A | T | 1 | a0001c0001t0001g0007 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.302+109T>A | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326365 | ||||||
| chr13:77326405
|
G | A | 2 | a0001c0009t0001g0310a0001c0009t0001g0311 | 2 | NA18612.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.302+69C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326405 | ||||||
| chr13:77326451
|
G | A | 5 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314others(2): Show | 5 | HG01884.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.302+23C>T | MYCBP2 | ENSG00000005810.20 | transcript | ENST00000544440.7 | protein_coding | 1/82 | chr13 | 77326451 |